NZ717492B2 - Administration of kynurenine depleting enzymes for tumor therapy - Google Patents

Abstract

Methods and compositions related to the use of a protein with kynureninase activity are described. For example, in certain aspects there may be disclosed a modified kynureninase capable of degrading kynurenine. Furthermore, certain aspects of the invention provide compositions and methods for the treatment of cancer with kynurenine depletion using the disclosed proteins or nucleic acids. eatment of cancer with kynurenine depletion using the disclosed proteins or nucleic acids.

Description

DESCRIPTION ADMINISTRATION OF KYNURENINE DEPLETING ENZYMES FOR TUMOR THERAPY BACKGROUND OF THE INVENTION The present application claims the priority benefit of United States provisional application numbers 61/872,132, filed August 30, 2013 and 61/986,366, filed April 30, 2014, the entire contents of which are incorporated herein by nce.

The invention was made with government support under Grant No. R01 CA154754 awarded by the National Institutes of Health. The government has certain rights in the invention. 1. Field of the Invention The invention lly relates to compositions and methods for the treatment of cancer with enzymes that deplete renine or Lhydroxykynurenine. More particularly, it concerns the engineering, pharmacological optimization and use of bacterial and mammalian s with L-kynurenine degrading activity suitable for human therapy. 2. Description of Related Art Overexpression of indolamine—2,3—dioxygenase isoforms (IDOl or ID02) by cancer cells or reprogramming of cancer infiltrating leukocytes to express either of these enzymes has been shown to have a profound effect on attenuating adaptive immune responses to cancer. IDOl and ID02 as well as the enzyme tryptophan 2,3—dioxygenase (TDO), whose expression by stromal cells may be induced by some tumors, catalyze the rate limiting step in tryptophan (Trp) catabolism to L-kynurenine (KYN) (Godin—Ethier et all, 2011). Tumors exchange a cytosolic KYN molecule for an extracellular Trp le using a LATl-like amino acid exchanger (Kaper et al., 2007), which has the dual effect on immune cells of locally elevating levels of KYN while locally depleting Trp levels. Neighboring immune cells internalize KYN, where it is an activating ligand for the aryl hydrocarbon or (AHR) resulting in the expression of numerous nes and chemokines that lead to tumor nce through immune cell differentiation and/or induction of apoptosis (Della Chiesa et al, 2006; Opitz et al., 2011; Song et al, 2011). Additionally, other KYN-related nds formed from kynurenine, most notably kynurenic acid also exert an immunosuppressive effect by serving as agonists of the orphan GPCR GPCR35. Inhibition of KYN formation (and thus inhibition of the formation of KYN metabolism byproducts, including kynurenic acid, 3-hydroxyl nine and quinolinic acid, via the inhibition of IDOl or TDO has received a significant amount of attention as a cancer target (Chen and Guillemin, 2009; Rutella et al., 2009; Prendergast, 2011). Substrate analog inhibitors, such as l-DL-methyltryptophan, for IDOl have been developed and have shown initial promise in overcoming cancer induced tumor tolerance thus restoring the ability of the native immune system to fight tumors (Lob et ai, 2009). However, KYN is also produced by tryptophan 2,3—dioxygenase (TDO), which is also frequently expressed in tumors and this enzyme is not inhibited by 1—DL—methyltryptophan (Pilotte er al., 2012). There are also additional concerns with the D-isomer of 1-DL-methyltryptophan (l-D-MT) currently in phase 1 and 2 clinical . xically, 1—D-MT can late IDOl expression, actually sing KYN levels and inducing suppression in certain cancers (Opitz et al., 2011).

Controlling tumor production of KYN is the focus of much research and has the potential to treat, among others, cancers such as breast cancer, n, glioblastoma, and pancreatic oma. KYN is known to suppresses proliferation as well as induce apoptosis in T cells and NK cells (Opitz et al., 2011; Mandi and , 2012) ng tumors to evade detection and destruction by a patient’s immune system. KYN is a potent ligand of the aryl hydrocarbon receptor (AHR) whose activation in T cells induces differentiation into CD25+FoxP3+ T regulatory cells (Tregs) (Mezrich et al., 2010). KYN has also been shown to prevent cytokine mediated up-regulation of specific receptors (NKp46 and NKG2D) required for NK mediated cell killing tumor cell lines (Della Chiesa et al, 2006), an action that is also likely mediated by its agonistic effect on AHR (Shin er (1]., 2013). There is also clinical evidence linking elevated serum KYN levels and decreased survival in multiple types of cancer. In healthy patients, KYN levels in serum are in the range of 0.5 to 1 uM. In patients with cancer types that produce KYN, such as diffuse large B-cell lymphoma, serum KYN levels were measured to be as much as 10 times higher (Yoshikawa et al., 2010; de Jong er al, 2011; Yao et al, 2011) and were prognostic for survival among lymphoma patients receiving the same treatment regimen; those with serum levels below 1.5 uM exhibited a 3 year survival rate of 89%, compared to only 58% al for those with KYN levels above 1.5 uM. This difference in survival was attributed to the immune suppressing effects of KYN kawa er al., 2010). The use of small le IDO inhibitors, such as 1—D-MT, has demonstrated the utility of controlling KYN levels in restoring immune function, but the off target effects of IDOl up-regulation by 1-D—MT and lack of inhibition for TDO and the IDOl isoform are of concern.

The present invention discloses the use enzymes for the specific depletion of KYN and its metabolites in tumors and/or in the blood. KYN depleting enzymes are used to lower KYN concentrations for the treatment of tumors expressing IDOl, ID02, or TDO thus preventing tumor—mediated tolerogenic s and d mediating tumor-ablating pro- atory responses. Notably, the use of enzymes for the depletion of KYN and KYN metabolic byproducts circumvents the ms associated with small molecule tors of IDO ms and TDO discussed above and further completely circumvents off target effects that are very commonly any small molecule drugs and lead to unpredicted ties and side effects.

SUMMARY OF THE INVENTION Aspects of the present invention overcome a major deficiency in the art by providing enzymes that comprise bacterial and mammalian polypeptide sequences capable of degrading L-kynurenine and 3-hydroxy-L-kynurenine and displaying favorable pharmacokinetics in serum as desired for cancer y. In some aspects, the kynureninase enzyme may have greater catalytic ty towards kynurenine than 3’OH-kynurenine. A kynureninase from a bacterial species may be used. Such an enzyme may have an amino acid sequence selected from the group consisting of SEQ ID NOs: 7 and 13—52 or a modified version thereof. In particular, the therapeutic may be d from the Pseudomonas fluorescens enzyme, kynureninase (Pf-KYNU). Alternatively, a kynureninase from Saccharomyces cerevisiae or pora crassa may be used. The therapeutic may be derived from the Mucilagz’nibacter paludis kynureninase enzyme. Further, to prevent adverse effects due to the immunogenicity of heterologous kynureninases, the Homo sapiens enzyme or other primate kynureninases displaying >95% ce identity to the human enzyme may be used. For example, a novel enzyme may have an amino acid sequence selected from the group consisting of SEQ ID NOs: 7-9.

In other s, there may be a polypeptide comprising either a native or modified human or primate kynureninase capable of degrading KYN and having activity towards the degradation of 3—hydroxykynurenine or kynurenic acid. In some embodiments, the polypeptide may be capable of degrading KYN under physiological conditions. For example, the polypeptide may have a catalytic ncy for KYN (km/KM) of at least or about 0.01, 0.05, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 2000, 3000, 4000, 5000, 6000, 7000, 8000, 9000, 104, 105, 106 M’ls’l or any range derivable therein.

A modified polypeptide as discussed above may be characterized as having a certain percentage of identity as compared to an unmodified ptide (e.g., a native polypeptide) or to any polypeptide sequence disclosed herein. For example, the unmodified polypeptide may comprise at least, or up to, about 150, 200, 250, 300, 350, 400 residues (or any range derivable therein) of a native ninase. The percentage identity may be about, at most or at least 40%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or 100% (or any range derivable n) n the modified and unmodified polypeptides, or between any two sequences in comparison. It is also contemplated that percentage of identity sed above may relate to a particular modified region of a polypeptide as compared to an unmodified region of a ptide. For instance, a polypeptide may contain a modified or mutant substrate ition site of a kynureninase that can be characterized based on the ty of the amino acid sequence of the modified or mutant substrate recognition site of the kynureninase to that of an unmodified or mutant kynureninase from the same species or across the species. A modified or mutant human polypeptide characterized, for example, as having at least 90% identity to an unmodified kynureninase means that at least 90% of the amino acids in that modified or mutant human polypeptide are identical to the amino acids in the fied polypeptide.

Such an unmodified polypeptide may be a native kynureninase, particularly a human isoform or other primate isoforms. For example, the native human kynureninase may have the ce of SEQ ID NO: 8. Non—limiting examples of other native primate kynureninase include Pongo abeliz' kynureninase (Genbank ID: XP_002812508.1; SEQ ID NO: 10), Macaca fascicufaris kynureninase (Genbank ID: EHH54849.1; SEQ ID NO: 11), and Pan troglodytes kynureninase (Genbank ID: 309314.1; SEQ ID NO: 12).

Exemplary native polypeptides include a sequence having about, at most or at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or 100% identity (or any range derivable therein) of SEQ ID NO: 8 or 10-12 or a fragment thereof. For example, the native polypeptide may comprise at least or up to about 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 150, 200, 250, 300, 350, 400, 415 residues (or any range derivable therein) of the sequence of SEQ ID NO: 8 or 10—12.

In some embodiments, the native kynureninase may be d by one or more other modifications, such as chemical ations, substitutions, ions, deletions, and/or truncations. For example, the modifications may be at a substrate recognitions site of the native enzyme. In a particular embodiment, the native kynureninase may be modified by substitutions. For example, the number of substitutions may be one, two, three, four or more.

In further embodiments, the native kynureninase may be modified in the substrate recognition site or any location that may affect substrate specificity.

[0012] In one embodiment, an isolated, modified human kynureninase enzyme is provided, wherein the modified enzyme has at least one substitution ve to native human kynureninase (see SEQ ID NO: 8), and wherein the at least one substitution includes a Met or Leu substitution for a Phe normally found at on 306 of native human kynureninase.

Thus, in one aspect, an isolated, modified human kynureninase enzyme is provided that comprises a Phe306Met substitution. In another aspect, an isolated, modified human kynureninase enzyme is provided that comprises a Phe306Leu substitution.

In some aspects, the present invention also contemplates polypeptides comprising a kynureninase linked to a heterologous amino acid sequence. For example, the kynureninase may be linked to the heterologous amino acid sequence as a fusion protein. In a particular embodiment, the ninase may be linked to amino acid sequences, such as an IgG Fc, n, an albumin binding protein, or an XTEN polypeptide for increasing the in vivo half-life.

To increase serum stability, the kynureninase may be linked to one or more polyether molecules. In a particular embodiment, the her may be polyethylene glycol (PEG). The polypeptide may be linked (e.g., covalently) to PEG via c amino acid residues, such as lysine or ne. For eutic administration, such a polypeptide comprising the kynureninase may be dispersed in a ceutically acceptable carrier.

In some aspects, a nucleic acid ng such a kynureninase is contemplated.

In some embodiments, the nucleic acid has been codon optimized for expression in bacteria.

In particular embodiments, the bacteria is E. coli. In other aspects, the nucleic acid has been codon zed for expression in fungus (e.g., yeast), insects, or mammals. The present invention r contemplates vectors, such as expression vectors, containing such nucleic acids. In particular embodiments, the nucleic acid encoding the kynureninase is operably linked to a promoter, including but not limited to heterologous promoters. In one embodiment, a kynureninase may be delivered to a target cell by a vector (e.g., a gene therapy vector). Such viruses may have been modified by recombinant DNA technology to enable the expression of the kynureninase—encoding nucleic acid in the target cell. These vectors may be derived from vectors of non—viral (e.g., ds) or viral (e.g., adenovirus, adeno-associated virus, retrovirus, lentivirus, herpes virus, or ia virus) origin. Non- viral vectors are preferably complexed with agents to facilitate the entry of the DNA across the cellular membrane. Examples of such non—viral vector complexes include the formulation with polycationic agents which facilitate the sation of the DNA and lipid- based delivery s. An e of a lipid—based delivery system would e liposome based delivery of nucleic acids.

In still r aspects, the present invention further contemplates host cells comprising such s. The host cells may be bacteria (e.g., E. coli), fungal cells (e.g., yeast), insect cells, or mammalian cells.

In some embodiments, the vectors are uced into host cells for expressing the kynureninase. The proteins may be expressed in any suitable manner. In one embodiment, the ns are expressed in a host cell such that the protein is glycosylated. In another embodiment, the proteins are expressed in a host cell such that the protein is aglycosylated.

Certain aspects of the present invention also contemplate methods of treatment by the administration of the kynureninase peptide, the nucleic acid ng the kynureninase in a gene therapy vector, or the formulation of the present invention, and in particular methods of treating tumor cells or subjects with cancer. The subject may be any animal, such as a mouse. For example, the subject may be a mammal, particularly a e, and more particularly a human patient. In some embodiments, the method may comprise selecting a patient with cancer.

In some embodiments, the cancer is any cancer that is sensitive to nine depletion. In one embodiment, the present invention contemplates a method of treating a tumor cell or a cancer patient comprising administering a formulation comprising such a polypeptide. In some embodiments, the administration occurs under conditions such that at least a portion of the cells of the cancer are killed. In another embodiment, the formulation comprises such a kynureninase with kynurenine-degrading activity at logical conditions and further comprising an attached polyethylene glycol chain. In some embodiment, the formulation is a pharmaceutical formulation comprising any of the above discussed kynureninases and pharmaceutically acceptable excipients. Such pharmaceutically acceptable excipients are well known to those of skill in the art. All of the above ninases may be contemplated as useful for human y.

In a further embodiment, there may also be provided a method of treating a tumor cell comprising administering a formulation comprising a non-bacterial (mammalian, e.g., primate or mouse) kynureninase that has kynurenine-degrading activity or a nucleic acid ng thereof.

The administration or treatment may be directed to the nutrient source for the cells, and not necessarily the cells themselves. Therefore, in an in vivo application, treating a tumor cell includes contacting the nutrient medium for a population of tumor cells with the kynureninase. In this embodiment, the medium can be blood, lymphatic fluid, spinal fluid and the like bodily fluid where nine depletion is desired.

In accordance with certain aspects of the present invention, such a formulation containing the kynureninase can be administered intravenously, intradermally, rterially, intraperitoneally, intralesionally, intracranially, rticularly, intraprostaticaly, intrapleurally, intrasynovially, intratracheally, asally, intravitreally, intravaginally, intrarectally, umorally, intramuscularly, subcutaneously, subconjunctival, intravesicularlly, mucosally, intrapericardially, intraumbilically, intraocularly, orally, topically, by inhalation, infusion, continuous infusion, localized perfusion, via a catheter, via a lavage, in lipid compositions (e.g., liposomes), or by other method or any combination of the forgoing as would be known to one of ordinary skill in the art.

In a further embodiment, the method may also comprise administering at least a second ncer therapy to the subject. The second ncer therapy may be a surgical therapy, herapy, radiation therapy, cryotherapy, hormone therapy, immunotherapy or cytokine therapy. In n aspects, the second anticancer therapy may be an anti-PD-l, anti-CTLA-4, or anti- PD-Ll antibody.

In some embodiment, a cell comprising a chimeric antigen receptor (CAR) and a kynureninase enzyme are contemplated for use in treating a t with cancer. In some aspects, the cell may be ected with a DNA encoding the CAR and the kynureninase and, in some cases, a transposase.

The CAR may target any cancer-cell antigen of interest, ing, for example, HER2, CD19, CD20, and GD2. The antigen binding regions or domain can se a fragment of the VH and VL chains of a single-chain variable fragment (scFv) derived from a particular human monoclonal antibody, such as those bed in US. Patent 7,109,304, which is incorporated herein by reference in its entirety. The fragment can also be any number of different antigen binding domains of a human antigen-specific antibody. In a more specific embodiment, the fragment is an antigen—specific scFv encoded by a ce that is optimized for human codon usage for expression in human cells. For additional examples of CARs, see, for e, WO 2012/031744, WO 2012/079000, WO 2013/059593, and US. Patent 8,465,743, all of which are incorporated herein by nce in their entireties.

The kynureninase may be any kynureninase disclosed herein. Methods of transfecting of cells are well known in the art, but in certain aspects, highly efficient transfections methods such as electroporation are employed. For example, nucleic acids may be introduced into cells using a nucleofection apparatus. Preferably, the transfection step does not involve infecting or transducing the cells with virus, which can cause xicity and/or lead to an immune response to cells ning viral sequences in a treated subject.

A wide range of CAR constructs and expression vectors for the same are known in the art and are r detailed herein. For example, in some aspects, the CAR expression vector is a DNA sion vector such as a plasmid, linear expression vector or an episome. In some aspects, the vector comprises additional sequences, such as sequence that facilitates expression of the CAR, such a promoter, enhancer, poly-A signal, and/or one or more introns. In preferred aspects, the CAR coding sequence is flanked by transposon sequences, such that the presence of a transposase allows the coding sequence to integrate into the genome of the transfected cell.

[0028] In certain aspects, cells are further transfected with a transposase that tates integration of a CAR coding sequence into the genome of the transfected cells. In some aspects, the transposase is provided as DNA expression . However, in red s, the transposase is provided as an expressible RNA or a protein such that long—term expression of the transposase does not occur in the transgenic cells. Any transposase system may be used in accordance with the embodiments. In other aspects, cells may be infected with a lentivirus to tate integration of the CAR coding sequence and the kynureninase coding sequence into the genome of the cell.

In one embodiment, a ition comprising a ninase or a nucleic acid encoding a kynureninase is provided for use in the treatment of a tumor in a subject. In another ment, the use of a kynureninase or a c acid encoding a kynureninase in the manufacture of a medicament for the treatment of a tumor is provided. Said kynureninase may be any kynureninase of the embodiments.

Embodiments discussed in the context of methods and/or compositions of the invention may be employed with respect to any other method or ition described herein. Thus, an embodiment pertaining to one method or composition may be applied to other methods and compositions of the invention as well.

As used herein the terms “encode” or “encoding,” with reference to a nucleic acid, are used to make the invention readily understandable by the skilled n; however, these terms may be used interchangeably with “comprise” or “comprising,” respectively.

As used herein the specification, “a” or “an” may mean one or more. As used herein in the claim(s), when used in conjunction with the word “comprising”, the words “a” or “an” may mean one or more than one.

The use of the term “or” in the claims is used to mean “and/or” unless itly indicated to refer to alternatives only or the alternatives are mutually exclusive, although the disclosure supports a definition that refers to only alternatives and “and/or.” As used herein “another” may mean at least a second or more.

Throughout this application, the term “about” is used to indicate that a value includes the inherent variation of error for the device, the method being employed to determine the value, or the variation that exists among the study subjects.

Other s, features and advantages of the present invention will become apparent from the following detailed description. It should be understood, however, that the detailed description and the specific examples, while indicating red embodiments of the invention, are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS The following drawings form part of the present specification and are included to further demonstrate certain s of the present invention. The invention may be better understood by nce to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.

— SDS-PAGE of (lane 1) PRECISION PLUS PROTEINTM MW standard (BioRad) (lanes 2-4) increasing concentrations of Pf—KYNU and (lane 5) PEG 5,000 MW modified Pf—KYNU.

[0038] — Stability of U in (open square) PBS and (open circle) pooled human serum. — y of —KYNU in an autologous B16 mouse melanoma model as measured by tumor growth rates. (Solid square) Heat inactivated —KYNU.

(Solid circle) Active PEG—Pf—KYNU.

[0040] — Efficacy of —KYNU in an autologous B16 mouse melanoma model as measured by survival. (Solid square) Heat vated PEG-Pf—KYNU. (Solid circle) Active PEG—Pf—KYNU.

FIGS. SA-B — Mice treated with heat-inactivated PEG-Pf—KYNU. (0) Mice treated with active PEG—Pf—KYNU. - The population of circulating CD4+ regulatory T-cell is significantly smaller in the group treated with active PEG—Pf—KYNU.

FIG SB — The population of tumor infiltrating CD8+ T—cells shows significantly higher expression of granzyme B and interferon y.

— Genetic ion for kynureninase activity in E. 0011‘. E. trpE cells plated on M9 minimal media plates with filter paper disks soaked in L—Trp (Trp), buffer (—), anthranilic acid (AA), or L-Kyn (Kyn).

— In vitro stability of Mucilaginibacter paludz’s kynureninase (Mu- KYNU). Activity as a function of time of Mu-KYNU (open square) in PBS at 37 °C with a 1T1/2 = 6 h with an amplitude of 74% remaining activity and a subsequent 2Tm = 150 h, and (solid circle) in pooled human serum at 37 °C with a 1T“; = 5 h with an amplitude of 30% remaining activity and a subsequent 2T1/2 = 73 h.

— Kaplan-Meier plot of B16 afts in C57BL/6J treated with either PEG-Pf-KYNU (no), deactivated PEG—Pf—KYNU (40), anti-PDl (00.), or anti—CTLA—4 (—). Arrows indicate treatment days, (A) indicates treatment with antibody, (E) indicates treatment with .

FIGS. 9A-C — — C57BL/6J bearing B16 tumor allografts treated with PBS (circle) (control), anti-PDl alone (square), anti-PDl/PEG—Mu—KYNU (upside—down triangle), or anti-PDl/PEG-Pf—KYNU (right-side up le). — Additive effects were observed with anti-PDl/PEG—Pf—KYNU combination treatment eliminating 60% of tumors and anti-PDl/PEG—Mu-KYNU combination eliminating 20% of tumors compared to 0% tumor elimination with anti-PDl alone. - Corresponding Kaplan-Meier plot.

FIGS. 10A-B — A - 6J bearing B16 tumor allografts treated with heat—inactivated PEG-Mu-KYNU (I) or active PEG-Mu-KYNU (A). B — Corresponding -Meier plot ing a median al time of 25 days for PEG-Mu- KYNU (-——), and median survival time of 22 days for heat—inactivated PEG-Mu-KYNU (—) (arrows indicate treatment days).

PTION OF ILLUSTRATIVE EMBODIMENTS

[0047] Kynurenine is a metabolite of the amino acid tryptophan generated via the action of either indolamine-2,3-dioxygenase (IDO) or tryptophan-2,3-dioxygenase (TDO).

Kynurenine exerts multiple effects on cell logy, one of the most important of which is modulation of T cell responses. Many tumor cells regulate the synthesis of IDO and/or TDO to elevate the local concentration of kynurenine, which is accompanied with depletion of tryptophan. High levels of kynurenine serve as a powerful way to inhibit the function of tumor infiltrating T cells that would ise attack the tumor.

The present invention provides methods for the use of kynurenine degrading enzymes as a means for depleting local kynurenine levels in the tumor microenvironment as well as in the serum and thus prevent mediated suppression of T—cell action.

Kynurenine hydrolyzing enzymes (kynureninases) convert kynurenine to alanine and anthranilic acid, the latter of which is not known to affect T-cell function. The inventors generated a pharmaceutical preparation of kynureninase enzyme to enable the enzyme to persist for prolonged times under physiological conditions. The inventors then showed that intratumoral administration of the enzyme results in dramatic retardation of growth of an aggressive tumor in mice. 1. ions As used herein the terms “protein” and “polypeptide” refer to compounds sing amino acids joined via peptide bonds and are used hangeably.

[0050] As used herein, the term “fusion protein” refers to a chimeric protein containing proteins or protein fragments operably linked in a non-native way.

As used herein, the term “half-life” (1/2-life) refers to the time that would be required for the concentration of a polypeptide thereof to fall by half in vitro or in viva, for example, after injection in a mammal.

[0052] The terms “in operable combination,3, LL’ 1n operable order,” and “operably linked” refer to a linkage wherein the components so described are in a relationship permitting them to on in their intended manner, for example, a linkage of nucleic acid sequences in such a manner that a c acid molecule capable of directing the transcription of a given gene and/or the synthesis of desired protein molecule, or a e of amino acid sequences in such a manner so that a fusion protein is produced.

The term r” is meant to refer to a compound or moiety that acts as a lar bridge to operably link two different molecules, wherein one portion of the linker is ly linked to a first molecule, and n another portion of the linker is operably linked to a second molecule.

The term ated” refers to conjugation with polyethylene glycol (PEG), which has been widely used as a drug carrier, given its high degree of biocompatibility and ease of modification. PEG can be d (e.g., covalently linked) to active agents through the hydroxy groups at the end of the PEG chain via chemical s; r, PEG itself is limited to at most two active agents per molecule. In a different approach, copolymers of PEG and amino acids have been explored as novel biomaterial that would retain the biocompatibility of PEG, but that would have the added advantage of numerous attachment points per molecule (thus providing greater drug loading), and that can be synthetically designed to suit a variety of applications.

[0055] The term “gene” refers to a DNA sequence that comprises control and coding sequences necessary for the production of a polypeptide or sor thereof. The polypeptide can be encoded by a full—length coding sequence or by any n of the coding sequence so as the desired enzymatic activity is retained.

The term “native” refers to the typical form of a gene, a gene product, or a characteristic of that gene or gene product when isolated from a naturally occurring source.

A native form is that which is most frequently observed in a natural population and is thus arbitrarily designated the normal or wild-type form. In contrast, the term “modified,” “variant,” or “mutant” refers to a gene or gene product that displays modification in sequence and functional properties (i.e., d characteristics) when compared to the native gene or gene product.

The term “vector” is used to refer to a carrier nucleic acid molecule into which a nucleic acid sequence can be inserted for introduction into a cell where it can be replicated.

A nucleic acid sequence can be “exogenous,” which means that it is foreign to the cell into which the vector is being uced or that the sequence is homologous to a sequence in the cell but in a position within the host cell nucleic acid in which the sequence is ordinarily not found. Vectors include plasmids, s, viruses (bacteriophage, animal s, and plant viruses), and artificial chromosomes (e.g., YACs). One of skill in the art would be well equipped to construct a vector through standard recombinant techniques (see, for example, Maniatis et al., 1988 and Ausubel et al, 1994, both incorporated herein by reference).

[0058] The term “expression vector” refers to any type of c uct comprising a nucleic acid coding for an RNA capable of being transcribed. In some cases, 2014/053437 RNA molecules are then translated into a protein, polypeptide, or peptide. In other cases, these sequences are not translated, for example, in the production of antisense molecules or mes. Expression vectors can contain a variety of “control sequences,” which refer to nucleic acid sequences ary for the transcription and possibly translation of an operably linked coding sequence in a particular host cell. In addition to control sequences that govern transcription and translation, vectors and expression vectors may contain nucleic acid ces that serve other ons as well and are described infra.

The term “therapeutically effective amount” as used herein refers to an amount of cells and/or therapeutic composition (such as a therapeutic polynucleotide and/or therapeutic polypeptide) that is employed in methods to achieve a therapeutic effect. The term “therapeutic benefit” or peutically effective” as used throughout this application refers to anything that promotes or enhances the well-being of the subject with t to the medical treatment of this condition. This includes, but is not limited to, a reduction in the frequency or severity of the signs or symptoms of a disease. For example, treatment of cancer may involve, for example, a reduction in the size of a tumor, a reduction in the invasiveness of a tumor, reduction in the growth rate of the cancer, or prevention of metastasis. Treatment of cancer may also refer to prolonging al of a subject with cancer.

The term “KM” as used herein refers to the Michaelis-Menten constant for an enzyme and is defined as the concentration of the specific substrate at which a given enzyme yields one-half its maximum velocity in an enzyme catalyzed reaction. The term “ cat” as used herein refers to the turnover number or the number of substrate molecules each enzyme site converts to product per unit time, and in which the enzyme is g at maximum efficiency. The term “ cat/KM” as used herein is the specificity constant, which is a measure of how efficiently an enzyme converts a substrate into t.

The term ric antigen receptors (CARs),” as used herein, may refer to artificial T-cell receptors, ic T-cell receptors, or chimeric immunoreceptors, for example, and encompass engineered receptors that graft an artificial specificity onto a particular immune or cell. CARs may be employed to impart the specificity of a onal antibody onto a T cell, thereby allowing a large number of specific T cells to be generated, for example, for use in adoptive cell therapy. In specific ments, CARS direct specificity of the cell to a tumor associated antigen, for example. In some embodiments, CARS comprise an intracellular activation domain, a transmembrane domain, and an extracellular domain comprising a tumor associated antigen binding region. In paiticular aspects, CARs comprise fusions of single-chain variable fragments (scFV) derived from monoclonal dies (such as those described in US. Patent 7,109,304, which is incorporated herein by reference in its entirety), fused to CD3-zeta transmembrane and endodomains. The specificity of other CAR designs may be derived from ligands of receptors (e. g., peptides) or from pattern—recognition receptors, such as Dectins. In ular embodiments, one can target malignant B cells by redirecting the specificity of T cells by using a CAR specific for the B-lineage molecule, CD19. In certain cases, the spacing of the antigen—recognition domain can be modified to reduce activation-induced cell death. In certain cases, CARs comprise s for additional co-stimulatory ing, such as CD3- zeta, FcR, CD27, CD28, CD137, DAPlO, and/or 0X40. In some cases, molecules can be co- expressed with the CAR, including co-stimulatory molecules, reporter genes for imaging (e.g., for on emission tomography), gene products that conditionally ablate the T cells upon addition of a pro-drug, homing receptors, chemokines, chemokine receptors, cytokines, and cytokine receptors.

“Treatment” and “treating” refer to administration or application of a therapeutic agent to a t or performance of a procedure or modality on a subject for the purpose of obtaining a eutic benefit of a e or health-related condition. For example, a ent may include administration of a pharmaceutically effective amount of a kynureninase. ct” and “patient” refer to either a human or non-human, such as primates, mammals, and vertebrates. In particular embodiments, the subject is a human. 11. Kynureninase ptides

[0064] Some embodiments concern modified proteins and polypeptides. Particular embodiments concern a d protein or polypeptide that ts at least one functional ty that is comparable to the unmodified version, preferably, the kynurenine degrading activity or the 3’—hydroxy—kynurenine degrading activity. In further aspects, the protein or polypeptide may be further modified to increase serum stability. Thus, when the present application refers to the function or activity of “modified protein” or a “modified ptide,” one of ordinary skill in the art would understand that this es, for example, a protein or polypeptide that possesses an additional advantage over the unmodified protein or polypeptide, such as kynurenine degrading activity or 3’-hydroxy-kynurenine degrading activity. In certain embodiments, the unmodified protein or polypeptide is a native kynureninase, preferably a human kynureninase or the Pseudomonas fluorescens kynureninase. It is specifically plated that embodiments concerning a “modified protein” may be implemented with respect to a “modified polypeptide,” and Vice versa. ination of activity may be ed using assays familiar to those of skill in the art, particularly with respect to the protein's activity, and may include for comparison purposes, the use of native and/or recombinant versions of either the modified or unmodified protein or polypeptide.

In certain ments, a modified polypeptide, such as a modified kynureninase, may be identified based on its increase in nine and/or roxy- kynurenine degrading activity. For example, substrate recognition sites of the unmodified polypeptide may be fied. This identification may be based on structural analysis or homology analysis. A population of mutants involving modifications of such substrate recognition sites may be generated. In a further embodiment, s with increased nine degrading activity may be selected from the mutant population. Selection of desired mutants may include methods, such as ion of byproducts or products from nine degradation.

[0067] Modified proteins may possess deletions and/or substitutions of amino acids; thus, a protein with a on, a n with a substitution, and a protein with a deletion and a substitution are modified proteins. In some embodiments, these modified proteins may further include insertions or added amino acids, such as with fusion proteins or proteins with linkers, for e. A “modified deleted protein” lacks one or more residues of the native protein, but may possess the specificity and/or activity of the native protein. A “modified deleted protein” may also have reduced immunogenicity or antigenicity. An example of a d deleted protein is one that has an amino acid residue deleted from at least one antigenic region that is, a region of the protein determined to be antigenic in a particular organism, such as the type of organism that may be administered the modified protein.

[0068] Substitution or replacement variants typically contain the exchange of one amino acid for another at one or more sites within the n and may be designed to -l6- modulate one or more properties of the polypeptide, particularly its effector functions and/or bioavailability. Substitutions may or may not be vative, that is, one amino acid is replaced with one of similar shape and charge. Conservative substitutions are well known in the art and include, for example, the changes of: e to serine; ne to lysine; asparagine to glutamine or histidine; aspartate to glutamate; cysteine to serine; glutamine to asparagine; glutamate to aspartate; glycine to proline; histidine to asparagine or glutamine; isoleucine to leucine or valine; leucine to valine or isoleucine; lysine to arginine; methionine to leucine or isoleucine; phenylalanine to tyrosine, leucine, or methionine; serine to threonine; threonine to serine; tryptophan to tyrosine; tyrosine to tryptophan or phenylalanine; and valine to isoleucine or e.

In addition to a on or substitution, a modified protein may possess an insertion of residues, which typically involves the addition of at least one residue in the polypeptide. This may include the insertion of a targeting peptide or ptide or simply a single residue. Terminal additions, called fusion proteins, are discussed below.

[0070] The term gically functional equivalent” is well understood in the art and is further defined in detail herein. ingly, sequences that have between about 70% and about 80%, or between about 81% and about 90%, or even between about 91% and about 99% of amino acids that are identical or functionally equivalent to the amino acids of a control polypeptide are included, provided the biological activity of the protein is maintained.

A modified protein may be biologically functionally equivalent to its native counterpart in certain aspects.

It also will be tood that amino acid and nucleic acid sequences may include additional residues, such as additional N— or C—terminal amino acids or 5’ or 3' sequences, and yet still be essentially as set forth in one of the sequences disclosed herein, so long as the sequence meets the criteria set forth above, including the maintenance of biological protein ty where protein expression is ned. The on of terminal sequences particularly applies to nucleic acid ces that may, for example, include various non—coding sequences flanking either of the 5’ or 3’ portions of the coding region or may include various internal sequences, i.e., introns, which are known to occur within genes.

WO 31771 III. Enzymatic Kynurenine Degradation for Therapy In certain aspects, the ptides may be used for the treatment of diseases, including cancers that are sensitive to kynurenine depletion, with enzymes that deplete kynurenine, to prevent tumor-mediated tolerogenic effects and instead mediate tumor- ablating pro-inflammatory responses. In certain aspects, kynureninases are contemplated for use in treating tumors expressing IDO l, IDO2, and/or TDO.

Certain aspects of the present invention provide a modified kynureninase for treating diseases, such as tumors. ularly, the d polypeptide may have human polypeptide ces and thus may prevent allergic ons in human patients, allow repeated dosing, and increase the therapeutic efficacy.

Tumors for which the present treatment methods are useful include any malignant cell type, such as those found in a solid tumor or a hematological tumor.

Exemplary solid tumors can include, but are not limited to, a tumor of an organ selected from the group consisting of as, colon, cecum, stomach, brain, head, neck, ovary, kidney, larynx, sarcoma, lung, bladder, melanoma, prostate, and breast. Exemplary hematological tumors include tumors of the bone marrow, T or B cell malignancies, leukemias, lymphomas, blastomas, myelomas, and the like. Further examples of cancers that may be treated using the methods provided herein include, but are not limited to, carcinoma, lymphoma, blastoma, sarcoma, leukemia, squamous cell , lung cancer (including small-cell lung cancer, non- small cell lung cancer, adenocarcinoma of the lung, and squamous carcinoma of the lung), cancer of the peritoneum, hepatocellular cancer, gastric or stomach cancer (including gastrointestinal cancer and gastrointestinal stromal cancer), pancreatic cancer, glioblastoma, al cancer, ovarian cancer, liver , bladder cancer, breast cancer, colon cancer, colorectal cancer, endometrial or uterine carcinoma, salivary gland carcinoma, kidney or renal , prostate cancer, vulval cancer, thyroid , various types of head and neck , melanoma, cial spreading melanoma, o malignant melanoma, acral lentiginous melanomas, nodular melanomas, as well as B-cell lymphoma (including low grade/follicular non-Hodgkin's lymphoma (NHL); small lymphocytic (SL) NHL; intermediate grade/follicular NHL; intermediate grade diffuse NHL; high grade immunoblastic NHL; high grade lymphoblastic NHL; high grade small non-cleaved cell NHL; bulky disease NHL; mantle cell lymphoma; AIDS—related lymphoma; and Waldenstrom's macroglobulinemia), chronic lymphocytic leukemia (CLL), acute -l8- lymphoblastic leukemia (ALL), Hairy cell ia, multiple myeloma, acute myeloid leukemia (AML) and c myeloblastic leukemia.

The cancer may specifically be of the following histological type, though it is not limited to these: sm, malignant; oma; carcinoma, undifferentiated; giant and spindle cell carcinoma; small cell oma; papillary carcinoma; squamous cell oma; lymphoepithelial carcinoma; basal cell carcinoma; pilomatrix carcinoma; transitional cell carcinoma; papillary transitional cell carcinoma; adenocarcinoma; gastrinoma, malignant; cholangiocarcinoma; hepatocellular carcinoma; combined hepatocellular oma and cholangiocarcinoma; trabecular adenocarcinoma; adenoid cystic carcinoma; adenocarcinoma in atous polyp; adenocarcinoma, familial polyposis coli; solid carcinoma; carcinoid tumor, malignant; branchiolo-alveolar adenocarcinoma; papillary arcinoma; chromophobe carcinoma; acidophil carcinoma; oxyphilic arcinoma; basophil carcinoma; clear cell adenocarcinoma; granular cell carcinoma; follicular arcinoma; papillary and follicular adenocarcinoma; nonencapsulating sclerosing carcinoma; l cortical carcinoma; troid carcinoma; skin appendage carcinoma; ne adenocarcinoma; sebaceous adenocarcinoma; ceruminous adenocarcinoma; mucoepidermoid carcinoma; cystadenocarcinoma; papillary cystadenocarcinoma; papillary serous cystadenocarcinoma; mucinous cystadenocarcinoma; mucinous adenocarcinoma; signet ring cell carcinoma; infiltrating duct carcinoma; medullary carcinoma; r carcinoma; inflammatory oma; paget's disease, mammary; acinar cell carcinoma; adenosquamous carcinoma; adenocarcinoma W/squamous metaplasia; thymoma, malignant; ovarian stromal tumor, malignant; thecoma, malignant; granulosa cell tumor, malignant; androblastoma, malignant; sertoli cell carcinoma; leydig cell tumor, malignant; lipid cell tumor, malignant; paraganglioma, malignant; extra-mammary paraganglioma, malignant; pheochromocytoma; glomangiosarcoma; malignant melanoma; amelanotic melanoma; superficial spreading melanoma; malignant ma in giant pigmented nevus; epithelioid cell melanoma; blue nevus, malignant; sarcoma; fibrosarcoma; fibrous histiocytoma, malignant; rcoma; liposarcoma; leiomyosarcoma; rhabdomyosarcoma; embryonal rhabdomyosarcoma; alveolar rhabdomyosarcoma; stromal a; mixed tumor, malignant; mullerian mixed tumor; nephroblastoma; hepatoblastoma; carcinosarcoma; mesenchymoma, malignant; brenner tumor, malignant; phyllodes tumor, malignant; synovial sarcoma; mesothelioma, malignant; dysgerminoma; embryonal carcinoma; teratoma, malignant; struma ovarii, malignant; choriocarcinoma; mesonephroma, malignant; hemangiosarcoma; hemangioendothelioma, malignant; kaposi's sarcoma; hemangiopericytoma, malignant; lymphangiosarcoma; osteosarcoma; juxtacortical osteosarcoma; chondrosarcoma; oblastoma, ant; mesenchymal chondrosarcoma; giant cell tumor of bone; ewing's a; odontogenic tumor, malignant; ameloblastic odontosarcoma; ameloblastoma, malignant; lastic fibrosarcoma; pinealoma, malignant; chordoma; glioma, malignant; ependymoma; astrocytoma; protoplasmic astrocytoma; fibrillary astrocytoma; astroblastoma; glioblastoma; oligodendroglioma; oligodendroblastoma; primitive neuroectodermal; cerebellar sarcoma; ganglioneuroblastoma; neuroblastoma; retinoblastoma; olfactory neurogenic tumor; meningioma, malignant; lbrosarcoma; emmoma, malignant; granular cell tumor, malignant; malignant ma; hodgkin's disease; hodgkin’s; paragranuloma; malignant lymphoma, small lymphocytic; malignant ma, large cell, diffuse; malignant lymphoma, follicular; mycosis fungoides; other specified non-hodgkin's lymphomas; malignant histiocytosis; multiple myeloma; mast cell sarcoma; immunoproliferative small intestinal disease; leukemia; lymphoid leukemia; plasma cell leukemia; erythroleukemia; lymphosarcoma cell leukemia; myeloid leukemia; basophilic leukemia; eosinophilic leukemia; monocytic leukemia; mast cell leukemia; megakaryoblastic leukemia; myeloid a; and hairy cell leukemia.

The kynureninase may be used herein as an antitumor agent in a variety of modalities for depleting kynurenine and/or 3’-hydroxy-kynurenine from tumor tissue, or the circulation of a mammal with cancer, or for depletion of kynurenine where its depletion is considered desirable.

Depletion can be conducted in vivo in the circulation of a , in vitro in cases where kynurenine and roxy—kynurenine depletion in tissue culture or other biological mediums is desired, and in ex vivo ures where biological fluids, cells, or tissues are manipulated outside the body and subsequently returned to the body of the patient mammal. Depletion of nine from circulation, e media, biological fluids, or cells is conducted to reduce the amount of kynurenine accessible to the material being treated, and therefore comprises contacting the material to be depleted with a kynurenine-depleting amount of the kynureninase under kynurenine-depleting conditions as to e the ambient kynurenine in the al being contacted.

The ion may be directed to the nutrient source for the cells, and not necessarily the cells themselves. Therefore, in an in viva application, treating a tumor cell includes contacting the nutrient medium for a population of tumor cells with the kynureninase. In this embodiment, the medium may be blood, lymphatic fluid, spinal fluid and the like bodily fluid where kynurenine depletion is d.

Kynurenine- and 3’-hydroxy-kynurenine-depleting efficiency can vary widely depending upon the application, and typically depends upon the amount of kynurenine present in the material, the desired rate of depletion, and the tolerance of the material for exposure to kynureninase. Kynurenine and kynurenine metabolite levels in a material, and therefore rates of kynurenine and kynurenine metabolite depletion from the material, can readily be monitored by a variety of chemical and biochemical methods well known in the art. Exemplary kynurenine-depleting amounts are described r , and can range from 0.001 to 100 units (U) of kynureninase, preferably about 0.01 to 10 U, and more preferably about 0.1 to 5 U kyureninase per milliliter (mL) of material to be d. Typical dosages can be stered based on body weight, and are in the range of about 5—1000 U/kilogram (kg)/day, preferably about 5—100 U/kg/day, more preferably about 10—50 U/kg/day, and more preferably about 20-40 U/kg/day.

Kynurenine—depleting conditions are buffer and ature conditions compatible with the biological activity of a kynureninase, and include moderate temperature, salt, and pH conditions compatible with the enzyme, for example, physiological conditions. ary conditions include about 4—40 °C., ionic strength equivalent to about 0.05 to 0.2 M NaCl, and a pH of about 5 to 9, while physiological conditions are included.

In a particular embodiment, the invention contemplates methods of using a kynureninase as an antitumor agent, and therefore ses contacting a population of tumor cells with a therapeutically effective amount of kynureninase for a time period sufficient to inhibit tumor cell growth.

[0082] In one embodiment, the ting in vivo is accomplished by administering, by intravenous intraperitoneal, or intratumoral injection, a therapeutically effective amount of a physiologically ble composition comprising an kynureninase of this ion to a patient, thereby depleting the kynurenine source of the tumor cells present in the t.

A eutically effective amount of a kynureninase is a predetermined amount calculated to e the desired effect, i.e., to deplete kynurenine in the tumor tissue or in a patient's circulation, and thereby mediate a tumor-ablating pro-inflammatory response.

Thus, the dosage ranges for the stration of kynureninase of the invention are those large enough to produce the desired effect in which the symptoms of tumor cell division and cell cycling are reduced. The dosage should not be so large as to cause adverse side effects, such as hyperviscosity syndromes, pulmonary edema, tive heart failure, neurological effects, and the like. Generally, the dosage will vary with age of, condition of, sex of, and extent of the disease in the patient and can be ined by one of skill in the art. The dosage can be adjusted by the individual physician in the event of any complication.

The kynureninase can be administered parenterally by injection or by gradual infusion over time. The kynureninase can be administered intravenously, intraperitoneally, orally, intramuscularly, subcutaneously, avity, transdermally, dermally, can be delivered by altic means, can be injected ly into the tissue containing the tumor cells, or can be administered by a pump connected to a catheter that may contain a potential biosensor for kynurenine.

The therapeutic compositions containing kynureninase are conventionally administered intravenously, as by injection of a unit dose, for example. The term “unit dose” when used in reference to a therapeutic composition refers to physically discrete units suitable as unitary dosage for the subject, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect in ation with the required diluent, i.e., carrier, or vehicle.

[0086] The compositions are administered in a manner compatible with the dosage formulation, and in a therapeutically effective amount. The quantity to be administered depends on the subject to be treated, capacity of the subject's system to utilize the active ingredient, and degree of therapeutic effect desired. Precise amounts of active ient required to be administered depend on the judgment of the practitioner and are peculiar to each individual. However, suitable dosage ranges for systemic application are disclosed herein and depend on the route of administration. Suitable s for initial administration and r shots are also contemplated and are d by an initial administration followed by repeated doses at one or more hour intervals by a subsequent injection or other administration. Exemplary multiple administrations are bed herein and are particularly preferred to in continuously high serum and tissue levels of kynureninase and conversely low serum and tissue levels of kynurenine. Alternatively, continuous intravenous infusion ent to maintain concentrations in the blood in the ranges specified for in viva therapies are contemplated.

IV. Conjugates Compositions and methods of the present invention involve modified kynureninases, such as by forming conjugates with heterologous peptide segments or polymers, such as polyethylene glycol. In further aspects, the ninases may be linked to PEG to se the hydrodynamic radius of the enzyme and hence increase the serum persistence. In certain aspects, the disclosed polypeptide may be conjugated to any targeting agent, such as a ligand having the ability to specifically and stably bind to an al or or g site on a tumor cell (US. Patent Publ. 2009/0304666).

A. Fusion Proteins Certain embodiments of the present invention concern fusion proteins. These molecules may have a native or modified kynureninase linked at the N- or C-terminus to a heterologous domain. For example, fusions may also employ leader sequences from other species to permit the recombinant expression of a protein in a heterologous host. Another useful fusion includes the addition of a protein affinity tag, such as a serum albumin affinity tag or six histidine residues, or an immunologically active domain, such as an antibody epitope, preferably cleavable, to facilitate purification of the fusion protein. Non-limiting affinity tags include polyhistidine, chitin binding protein (CBP), e binding protein (MBP), and glutathione—S—transferase (GST).

In a particular ment, the kynureninase may be linked to a e that increases the in viva ife, such as an XTEN polypeptide (Schellenberger et (21., 2009), IgG Fc domain, albumin, or albumin binding peptide.

Methods of generating fusion ns are well known to those of skill in the art. Such proteins can be produced, for example, by de novo synthesis of the complete fusion protein, or by attachment of the DNA sequence encoding the heterologous domain, followed by expression of the intact fusion n.

Production of fusion ns that recover the functional activities of the parent proteins may be facilitated by connecting genes with a bridging DNA segment WO 31771 encoding a peptide linker that is spliced between the polypeptides connected in tandem. The linker would be of sufficient length to allow proper folding of the resulting fusion protein.

B. s In certain embodiments, the ninase may be ally conjugated using bifunctional cross-linking reagents or fused at the n level with peptide linkers.

Bifunctional cross-linking reagents have been extensively used for a variety of purposes, including preparation of affinity matrices, modification and ization of diverse structures, identification of ligand and receptor binding sites, and structural studies. Suitable peptide linkers may also be used to link the kynureninase, such as Gly-Ser linkers.

[0094] Homobifunctional reagents that carry two identical functional groups proved to be highly efficient in inducing cross-linking between cal and different macromolecules or subunits of a macromolecule, and linking of polypeptide ligands to their specific binding sites. Heterobifunctional reagents contain two different functional groups.

By taking advantage of the differential reactivities of the two different functional groups, cross—linking can be controlled both selectively and sequentially. The bifunctional cross— linking reagents can be divided ing to the specificity of their functional groups, e.g., amino-, sulfhydryl-, guanidine-, indole-, carboxyl-specific groups. Of these, reagents directed to free amino groups have become especially popular because of their commercial availability, ease of synthesis, and the mild reaction conditions under which they can be applied.

A majority of heterobifunctional cross-linking ts contain a primary amine-reactive group and a thiol-reactive group. In another e, heterobifunctional cross—linking reagents and methods of using the cross—linking ts are described (US.

Pat. No. 5,889,155, specifically incorporated herein by reference in its entirety). The cross- linking reagents combine a nucleophilic hydrazide e with an electrophilic maleimide residue, allowing ng, in one example, of des to free thiols. The cross-linking reagent can be ed to cross—link various onal groups.

Additionally, any other linking/coupling agents and/or mechanisms known to those of skill in the art may be used to combine kynureninase, such as, for example, antibody- antigen interaction, avidin biotin linkages, amide linkages, ester linkages, thioester linkages, ether linkages, thioether linkages, phosphoester linkages, phosphoramide linkages, anhydride linkages, disulfide linkages, ionic and hobic interactions, bispecific antibodies and antibody fragments, or combinations thereof.

It is preferred that a cross—linker having able stability in blood will be ed. Numerous types of disulfide—bond ning linkers are known that can be successfully employed to conjugate ing and therapeutic/preventative agents. Linkers that contain a disulfide bond that is sterically hindered may prove to give greater stability in vivo. These linkers are thus one group of linking .

In addition to ed cross-linkers, non-hindered s also can be employed in accordance herewith. Other useful cross—linkers, not considered to contain or generate a protected disulfide, include SATA, SPDP, and 2-iminothiolane (Wawrzynczak and Thorpe, 1987). The use of such cross—linkers is well understood in the art. Another embodiment involves the use of flexible s.

Once chemically conjugated, the e generally will be purified to separate the conjugate from unconjugated agents and from other inants. A large number of purification techniques are available for use in providing conjugates of a sufficient degree of purity to render them clinically useful.

] Purification s based upon size separation, such as gel filtration, gel permeation, or high performance liquid chromatography, will generally be of most use.

Other chromatographic techniques, such as Blue—Sepharose separation, may also be used.

Conventional methods to purify the fusion proteins from inclusion bodies may be useful, such as using weak detergents, such as sodium N—lauroyl—sarcosine (SLS).

C. PEGylation In certain aspects of the invention, methods and compositions related to PEGylation of kynureninase are disclosed. For example, the kynureninase may be PEGylated in accordance with the methods disclosed herein.

PEGylation is the process of covalent attachment of poly(ethylene glycol) polymer chains to another molecule, normally a drug or therapeutic protein.

PEGylation is ely achieved by incubation of a reactive derivative of PEG with the 2014/053437 target macromolecule. The nt attachment of PEG to a drug or therapeutic protein can “mask” the agent from the host's immune system (reduced immunogenicity and nicity) or increase the hydrodynamic size (size in solution) of the agent, which prolongs its circulatory time by reducing renal clearance. PEGylation can also provide water lity to hydrophobic drugs and ns.

The first step of the tion is the suitable functionalization of the PEG polymer at one or both terminals. PEGs that are activated at each terminus with the same reactive moiety are known as “homobifunctional,” whereas if the functional groups present are different, then the PEG derivative is referred as “heterobifunctional” or “heterofunctional.” The chemically active or activated derivatives of the PEG polymer are prepared to attach the PEG to the desired molecule.

The choice of the suitable onal group for the PEG derivative is based on the type of ble reactive group on the molecule that will be coupled to the PEG.

For proteins, typical reactive amino acids include lysine, cysteine, histidine, arginine, aspartic acid, glutamic acid, serine, threonine, and tyrosine. The N—terminal amino group and the C- terminal carboxylic acid can also be used.

] The techniques used to form first generation PEG tives are generally reacting the PEG polymer with a group that is reactive with hydroxyl groups, typically anhydrides, acid chlorides, chloroformates, and carbonates. In the second generation PEGylation chemistry more nt functional groups, such as aldehyde, esters, amides, etc, are made available for ation.

As applications of PEGylation have become more and more advanced and sophisticated, there has been an increase in need for heterobifunctional PEGs for conjugation. These heterobifunctional PEGs are very useful in linking two entities, where a hydrophilic, flexible, and biocompatible spacer is needed. Preferred end groups for heterobifunctional PEGs are maleimide, vinyl sulfones, pyridyl disulfide, amine, carboxylic acids, and NHS esters.

The most common ation agents, or linkers, are based on methoxy PEG (mPEG) molecules. Their activity depends on adding a protein-modifying group to the alcohol end. In some instances polyethylene glycol (PEG diol) is used as the precursor molecule. The diol is subsequently modified at both ends in order to make a hetero— or homo—dimeric PEG—linked molecule.

Proteins are generally PEGylated at nucleophilic sites, such as unprotonated thiols (cysteinyl residues) or amino groups. Examples of cysteinyl-specific modification reagents include PEG maleimide, PEG iodoacetate, PEG thiols, and PEG vinylsulfone. All four are strongly nyl-specific under mild ions and neutral to slightly alkaline pH but each has some drawbacks. The thioether formed with the maleimides can be somewhat unstable under alkaline conditions so there may be some limitation to formulation options with this . The carbamothioate linkage formed with iodo PEGs is more stable, but free iodine can modify ne residues under some ions. PEG thiols form disulfide bonds with protein thiols, but this linkage can also be unstable under alkaline conditions. PEG—vinylsulfone reactivity is relatively slow ed to maleimide and iodo PEG; however, the thioether linkage formed is quite stable. Its slower reaction rate also can make the PEG-vinylsulfone reaction easier to control.

[00109] Site-specific PEGylation at native cysteinyl residues is seldom carried out, since these es are usually in the form of disulfide bonds or are required for biological activity. On the other hand, site—directed mutagenesis can be used to incorporate cysteinyl tion sites for thiol—specific linkers. The cysteine mutation must be designed such that it is accessible to the PEGylation reagent and is still biologically active after PEGylation.

Amine-specific modification agents include PEG NHS ester, PEG tresylate, PEG aldehyde, PEG isothiocyanate, and several others. All react under mild conditions and are very c for amino groups. The PEG NHS ester is probably one of the more reactive agents; however, its high reactivity can make the PEGylation on difficult to l on a large scale. PEG aldehyde forms an imine with the amino group, which is then reduced to a secondary amine with sodium cyanoborohydride. Unlike sodium borohydride, sodium cyanoborohydride will not reduce disulfide bonds. However, this chemical is highly toxic and must be handled cautiously, particularly at lower pH where it becomes volatile.

[00111] Due to the multiple lysine residues on most proteins, site—specific tion can be a challenge. Fortunately, because these ts react with unprotonated amino groups, it is possible to direct the PEGylation to lower-pK amino groups by performing the reaction at a lower pH. Generally the pK of the alpha-amino group is 1-2 pH units lower than the n-amino group of lysine residues. By PEGylating the molecule at pH 7 or below, high selectivity for the N-terminus frequently can be attained. r, this is only feasible if the N—terminal portion of the protein is not required for biological activity.

Still, the pharmacokinetic benefits from PEGylation frequently outweigh a significant loss of in vitro ivity, resulting in a product with much greater in viva bioactivity regardless of PEGylation chemistry.

There are several ters to consider when developing a PEGylation procedure. Fortunately, there are y no more than four or five key parameters. The “design of experiments” approach to optimization of PEGylation conditions can be very useful. For thiol—specific PEGylation reactions, parameters to consider include: protein concentration, PEG—to-protein ratio (on a molar , temperature, pH, reaction time, and in some instances, the exclusion of oxygen. (Oxygen can contribute to intermolecular disulfide formation by the protein, which will reduce the yield of the PEGylated product.) The same factors should be considered (with the exception of oxygen) for amine—specific modification except that pH may be even more critical, particularly when targeting the N—terminal amino group.

For both amine- and thiol-specific modifications, the reaction conditions may affect the stability of the protein. This may limit the temperature, n tration, and pH. In addition, the reactivity of the PEG linker should be known before starting the PEGylation reaction. For example, if the PEGylation agent is only 70 percent active, the amount of PEG used should ensure that only active PEG les are counted in the protein-to-PEG reaction stoichiometry.

V. Proteins and Peptides In certain embodiments, the present invention concerns novel compositions comprising at least one n or peptide, such as a kynureninase. These es may be comprised in a fusion protein or conjugated to an agent as described supra.

As used herein, a protein or peptide generally , but is not limited to, a protein of greater than about 200 amino acids, up to a full length sequence translated from a gene; a polypeptide of greater than about 100 amino acids; and/or a peptide of from about 3 to about 100 amino acids. For convenience, the terms “protein, 35 $‘polypeptide,” and “peptide” are used interchangeably herein.

As used herein, an “amino acid residue” refers to any lly occurring amino acid, any amino acid derivative, or any amino acid mimic known in the art.

In certain embodiments, the residues of the protein or peptide are sequential, without any non-amino acids interrupting the sequence of amino acid residues. In other embodiments, the sequence may comprise one or more non—amino acid moieties. In particular embodiments, the sequence of residues of the protein or peptide may be interrupted by one or more non— amino acid moieties.

[00117] Accordingly, the term “protein or peptide” encompasses amino acid sequences comprising at least one of the 20 common amino acids found in naturally occurring ns, or at least one modified or unusual amino acid.

Proteins or peptides may be made by any que known to those of skill in the art, ing the expression of proteins, polypeptides, or peptides through rd molecular biological techniques, the isolation of proteins or peptides from natural sources, or the chemical synthesis of ns or peptides. The nucleotide and protein, polypeptide, and peptide sequences corresponding to various genes have been previously disclosed, and may be found at computerized databases known to those of ordinary skill in the art. One such database is the National Center for Biotechnology Information's k and GenPept databases (available on the world wide web at ncbi.nlm.nih.gov/). The coding regions for known genes may be amplified and/or sed using the ques disclosed herein or as would be known to those of ordinary skill in the art. Alternatively, various commercial ations of proteins, polypeptides, and es are known to those of skill in the art.

VI. Nucleic Acids and Vectors In certain s of the invention, nucleic acid sequences ng a kynureninase or a fusion protein containing a kynureninase may be disclosed. Depending on which expression system is used, nucleic acid sequences can be selected based on conventional methods. For example, if the kynureninase is derived from human kynureninase and contains multiple codons that are rarely utilized in E. 0011', then that may interfere with expression. Therefore, the respective genes or ts thereof may be codon optimized for E. coli expression. Various vectors may be also used to s the protein of interest. Exemplary vectors e, but are not limited, plasmid vectors, viral s, transposon, or liposome—based vectors.

VII. Host Cells ] Host cells may be any that may be transformed to allow the expression and secretion of kynureninase and conjugates thereof. The host cells may be bacteria, mammalian cells, yeast, or filamentous fungi. Various bacteria include Escherichia and Bacillus. Yeasts belonging to the genera Saccharomyces, Kiuyveromyces, Hansenula, or Pichia would find use as an appropriate host cell. Various species of filamentous fungi may be used as expression hosts, including the following genera: Aspergillus, Trichoderma, Neurospora, Penicillium, Cephalosporium, Achlya, Podospora, Endothz'a, Mucor, Cochliobolus, and Pyricularia.

Examples of usable host organisms include bacteria, e. g., Escherichia coli MC1061, derivatives of Bacillus subtilis BRBl (Sibakov et al., 1984), Staphylococcus aureus SA1123 (Lordanescu, 1975) or ococcus lividans od et al., 1985); yeasts, e.g., Saccharomyces cerevisiae AH 22 (Mellor et al., 1983) or Schizosaccharomyces pombe; and filamentous fungi, e.g., Aspergillus hidulans, Aspergz'llus awamori (Ward, 1989), or Trichoderma reesei (Penttila et al., 1987; Harkki et al., 1989).

Examples of mammalian host cells e Chinese hamster ovary cells (CHO-Kl; ATCC CCL61), rat pituitary cells (GHl; ATCC CCL82), HeLa S3 cells (ATCC CCL2.2), rat hepatoma cells I—E; ATCCCRL 1548), SV40-transformed monkey kidney cells (COS—1; ATCC CRL 1650), and murine nic cells (NIH—3T3; ATCC CRL 1658). The ing being illustrative but not limitative of the many possible host organisms known in the art. In principle, all hosts capable of secretion can be used whether prokaryotic or eukaryotic. ian host cells expressing the kynureninase and/or their fusion proteins are cultured under conditions typically employed to culture the parental cell line.

Generally, cells are cultured in a standard medium containing physiological salts and nutrients, such as standard RPMI, MEM, IMEM, or DMEM, lly supplemented with 5%—10% serum, such as fetal bovine serum. Culture conditions are also standard, e.g., 2014/053437 cultures are incubated at 37 °C in stationary or roller cultures until desired levels of the proteins are achieved.

VIII. n Purification Protein ation ques are well known to those of skill in the art. These techniques involve, at one level, the homogenization and crude fractionation of the cells, tissue, or organ to polypeptide and non—polypeptide fractions. The protein or polypeptide of interest may be further purified using chromatographic and electrophoretic techniques to achieve partial or complete purification (or purification to neity) unless ise specified. Analytical methods particularly suited to the preparation of a pure peptide are ion-exchange chromatography, gel exclusion chromatography, polyacrylamide gel electrophoresis, affinity chromatography, immunoaffinity chromatography, and isoelectric focusing. A particularly efficient method of purifying peptides is fast-performance liquid chromatography (FPLC) or even high-performance liquid chromatography (HPLC).

A purified protein or peptide is intended to refer to a composition, isolatable from other components, wherein the protein or peptide is d to any degree relative to its naturally-obtainable state. An isolated or purified protein or peptide, therefore, also refers to a protein or peptide free from the nment in which it may naturally occur.

Generally, “purified” will refer to a protein or peptide composition that has been subjected to fractionation to remove various other components, and which composition substantially retains its sed biological activity. Where the term “substantially purified” is used, this designation will refer to a composition in which the protein or e forms the major component of the ition, such as constituting about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, or more of the proteins in the ition.

Various techniques suitable for use in protein purification are well known to those of skill in the art. These e, for example, precipitation with ammonium sulphate, PEG, antibodies and the like, or by heat denaturation, followed by centrifugation; chromatography steps, such as ion exchange, gel filtration, reverse phase, hydroxyapatite, and affinity chromatography; isoelectric focusing; gel electrophoresis; and combinations of these and other techniques. As is generally known in the art, it is believed that the order of conducting the various purification steps may be changed, or that certain steps may be omitted, and still result in a suitable method for the preparation of a substantially d protein or peptide.

Various methods for quantifying the degree of purification of the protein or peptide are known to those of skill in the art in light of the present disclosure.

These e, for example, determining the specific activity of an active fraction, or assessing the amount of polypeptides within a fraction by SDS/PAGE analysis. A preferred method for assessing the purity of a fraction is to calculate the specific ty of the fraction, to compare it to the c activity of the initial extract, and to thus calculate the degree of purity therein, assessed by a “—fold purification number.” The actual units used to represent the amount of activity will, of course, be dependent upon the particular assay technique chosen to follow the purification, and whether or not the sed protein or peptide exhibits a detectable activity.

There is no general requirement that the protein or e will always be provided in its most purified state. Indeed, it is contemplated that less substantially purified products may have utility in n embodiments. Partial purification may be accomplished by using fewer purification steps in combination, or by utilizing different forms of the same general ation scheme. For example, it is appreciated that a - exchange column chromatography performed ing an HPLC apparatus will generally result in a greater “-fold” purification than the same technique utilizing a low pressure chromatography system. Methods exhibiting a lower degree of relative purification may have advantages in total recovery of n product, or in maintaining the activity of an expressed protein.

In certain embodiments a protein or peptide may be isolated or purified, for example, a kynureninase, a fusion protein containing a kynureninase, or a modified kynureninase post PEGylation. For example, a His tag or an affinity e may be comprised in such a kynureninase to facilitate purification. Affinity chromatography is a chromatographic procedure that relies on the specific affinity between a substance to be isolated and a molecule to which it can specifically bind. This is a receptor-ligand type of interaction. The column material is synthesized by covalently coupling one of the binding partners to an insoluble matrix. The column material is then able to specifically adsorb the nce from the solution. n occurs by ng the conditions to those in which binding will not occur (e.g., d pH, ionic strength, temperature, etc). The matrix should -3 2- WO 31771 be a substance that does not adsorb molecules to any cant extent and that has a broad range of chemical, physical, and thermal stability. The ligand should be coupled in such a way as to not affect its binding properties. The ligand should also provide relatively tight binding. It should be possible to elute the substance without ying the sample or the ligand.

Size exclusion chromatography (SEC) is a chromatographic method in which molecules in on are separated based on their size, or in more technical terms, their hydrodynamic volume. It is usually applied to large molecules or macromolecular complexes, such as proteins and industrial polymers. Typically, when an s solution is used to transport the sample through the column, the technique is known as gel filtration chromatography, versus the name gel permeation chromatography, which is used when an organic solvent is used as a mobile phase.

The underlying principle of SEC is that particles of different sizes will elute (filter) h a stationary phase at different rates. This results in the separation of a solution of les based on size. Provided that all the particles are loaded simultaneously or near simultaneously, particles of the same size should elute together. Each size exclusion column has a range of molecular weights that can be separated. The exclusion limit defines the molecular weight at the upper end of this range and is where molecules are too large to be trapped in the stationary phase. The permeation limit defines the molecular weight at the lower end of the range of tion and is where molecules of a small enough size can ate into the pores of the stationary phase completely and all molecules below this molecular mass are so small that they elute as a single band.

High—performance liquid chromatography (or high—pressure liquid chromatography, HPLC) is a form of column chromatography used frequently in biochemistry and analytical chemistry to separate, identify, and quantify compounds. HPLC utilizes a column that holds chromatographic packing material (stationary phase), a pump that moves the mobile phase(s) through the , and a detector that shows the retention times of the molecules. ion time varies depending on the interactions n the stationary phase, the molecules being analyzed, and the solvent(s) used.

IX. Pharmaceutical Compositions It is contemplated that the novel kynureninase can be administered systemically or locally to inhibit tumor cell growth and, most preferably, to kill cancer cells in cancer patients with locally ed or metastatic cancers. They can be administered intravenously, intrathecally, and/or intraperitoneally. They can be administered alone or in combination with anti-proliferative drugs. In one embodiment, they are administered to reduce the cancer load in the patient prior to surgery or other procedures. Alternatively, they can be stered after surgery to ensure that any remaining cancer (e.g., cancer that the surgery failed to eliminate) does not e.

[00134] It is not intended that the present invention be limited by the particular nature of the therapeutic preparation. For example, such compositions can be provided in formulations er with physiologically tolerable liquid, gel, or solid carriers, diluents, and excipients. These therapeutic preparations can be stered to mammals for veterinary use, such as with domestic animals, and clinical use in humans in a manner r to other therapeutic agents. In general, the dosage ed for therapeutic efficacy will vary according to the type of use and mode of administration, as well as the particularized requirements of individual subjects.

Such compositions are typically prepared as liquid solutions or suspensions, as injectables. Suitable diluents and excipients are, for example, water, , dextrose, glycerol, or the like, and ations thereof. In addition, if desired, the compositions may contain minor amounts of auxiliary substances, such as wetting or emulsifying agents, stabilizing agents, or pH buffering agents.

Where clinical applications are contemplated, it may be necessary to prepare pharmaceutical compositions comprising proteins, antibodies, and drugs in a form appropriate for the intended application. Generally, pharmaceutical itions may comprise an effective amount of one or more kynureninase or additional agents dissolved or dispersed in a pharmaceutically acceptable carrier. The s “pharmaceutical or pharmacologically acceptable” refers to molecular entities and compositions that do not produce an adverse, allergic, or other untoward reaction when administered to an animal, such as, for example, a human, as riate. The ation of a pharmaceutical composition that contains at least one kyureninase ed by the method disclosed herein, or additional active ient will be known to those of skill in the art in light of the present disclosure, as exemplified by Remington's Pharmaceutical es, 18th Ed., 1990, incorporated herein by reference. Moreover, for animal (e.g., human) administration, it will be understood that preparations should meet sterility, pyrogenicity, general safety, and purity standards as required by the FDA Office of Biological Standards.

As used herein, “pharmaceutically acceptable carrier” includes any and all solvents, dispersion media, coatings, surfactants, antioxidants, preservatives (e.g., antibacterial agents, antifungal agents), isotonic agents, absorption delaying agents, salts, preservatives, drugs, drug stabilizers, gels, s, excipients, disintegration agents, lubricants, ning agents, ing agents, dyes, such like materials and combinations thereof, as would be known to one of ordinary skill in the art (see, for example, Remington's Pharmaceutical Sciences, 18th Ed., 1990, incorporated herein by reference). Except insofar as any conventional carrier is incompatible with the active ingredient, its use in the pharmaceutical itions is plated.

[00138] Certain embodiments of the present invention may comprise different types of rs depending on whether it is to be administered in solid, liquid, or aerosol form, and whether it needs to be sterile for the route of administration, such as injection. The compositions can be administered intravenously, intradermally, transdermally, hecally, intraarterially, intraperitoneally, intranasally, intravaginally, intrarectally, intramuscularly, subcutaneously, mucosally, orally, lly, locally, by inhalation (e.g., aerosol inhalation), by injection, by infusion, by continuous infusion, by localized ion bathing target cells directly, via a catheter, via a lavage, in lipid itions (e.g., liposomes), or by other methods or any combination of the forgoing as would be known to one of ordinary skill in the art (see, for e, Remington's Pharmaceutical Sciences, 18th Ed., 1990, incorporated herein by reference).

The modified polypeptides may be formulated into a ition in a free base, neutral, or salt form. Pharmaceutically acceptable salts include the acid addition salts, e.g., those formed with the free amino groups of a proteinaceous composition, or which are formed with nic acids, such as, for example, hydrochloric or phosphoric acids, or such organic acids as acetic, oxalic, tartaric, or mandelic acid. Salts formed with the free carboxyl groups can also be derived from inorganic bases, such as, for e, sodium, potassium, ammonium, calcium, or ferric hydroxides; or such organic bases as pylamine, hylamine, histidine, or procaine. Upon formulation, solutions will be administered in a manner compatible with the dosage formulation and in such amount as is therapeutically effective. The formulations are easily administered in a variety of dosage forms, such as formulated for eral administrations, such as injectable solutions, or aerosols for delivery to the lungs, or formulated for alimentary administrations, such as drug release capsules and the like.

] Further in accordance with certain aspects of the present invention, the composition suitable for administration may be provided in a pharmaceutically acceptable carrier with or without an inert diluent. The carrier should be assimilable and includes liquid, olid, i.e., pastes, or solid carriers. Except insofar as any conventional media, agent, diluent, or carrier is detrimental to the recipient or to the therapeutic effectiveness of a the ition contained therein, its use in administrable composition for use in practicing the methods is appropriate. es of carriers or diluents include fats, oils, water, saline ons, lipids, liposomes, resins, binders, s, and the like, or combinations thereof. The composition may also comprise various antioxidants to retard oxidation of one or more component. Additionally, the prevention of the action of microorganisms can be brought about by preservatives, such as various antibacterial and antifungal agents, including but not limited to parabens (e.g., methylparabens, propylparabens), chlorobutanol, phenol, sorbic acid, thimerosal or combinations thereof.

[00141] In accordance With certain aspects of the present invention, the composition is combined with the carrier in any convenient and practical manner, i.e., by solution, suspension, fication, admixture, encapsulation, absorption, and the like. Such procedures are routine for those d in the art.

In a specific embodiment of the present invention, the composition is combined or mixed ghly with a olid or solid carrier. The mixing can be carried out in any convenient manner, such as ng. Stabilizing agents can be also added in the mixing process in order to protect the composition from loss of therapeutic activity, i.e., denaturation in the stomach. Examples of stabilizers for use in a composition include buffers, amino acids, such as glycine and lysine, carbohydrates, such as dextrose, mannose, galactose, fructose, lactose, sucrose, maltose, sorbitol, mannitol, etc. -3 6- In further embodiments, the present invention may concern the use of a pharmaceutical lipid vehicle composition that includes kynureninases, one or more lipids, and an aqueous solvent. As used herein, the term “lipid” will be defined to include any of a broad range of substances that is characteristically ble in water and table with an c solvent. This broad class of compounds is well known to those of skill in the art, and as the term “lipid” is used herein, it is not limited to any particular structure. es include compounds that contain long-chain tic hydrocarbons and their derivatives. A lipid may be naturally occurring or synthetic (i.e., designed or produced by man). However, a lipid is usually a biological substance. Biological lipids are well known in the art, and include for example, neutral fats, phospholipids, phosphoglycerides, steroids, terpenes, lysolipids, glycosphingolipids, glycolipids, sulphatides, lipids with ether— and ester-linked fatty acids, polymerizable lipids, and combinations thereof. Of course, compounds other than those specifically described herein that are understood by one of skill in the art as lipids are also encompassed by the compositions and methods.

[00144] One of ordinary skill in the art would be familiar with the range of techniques that can be employed for dispersing a composition in a lipid vehicle. For e, the ninase or a fusion protein thereof may be sed in a on containing a lipid, dissolved with a lipid, emulsified with a lipid, mixed with a lipid, combined with a lipid, covalently bonded to a lipid, contained as a suspension in a lipid, contained or complexed with a micelle or liposome, or otherwise associated with a lipid or lipid structure by any means known to those of ordinary skill in the art. The dispersion may or may not result in the formation of liposomes.

The actual dosage amount of a composition administered to an animal patient can be determined by physical and logical factors, such as body weight, severity of condition, the type of disease being treated, previous or concurrent therapeutic interventions, idiopathy of the patient, and on the route of administration. Depending upon the dosage and the route of administration, the number of administrations of a preferred dosage and/or an effective amount may vary according to the se of the subject. The practitioner responsible for administration will, in any event, determine the concentration of active ingredient(s) in a composition and appropriate ) for the individual t.

In certain embodiments, pharmaceutical itions may comprise, for example, at least about 0.1% of an active compound. In other embodiments, an active WO 31771 compound may se between about 2% to about 75% of the weight of the unit, or between about 25% to about 60%, for example, and any range derivable therein. Naturally, the amount of active compound(s) in each therapeutically useful composition may be prepared in such a way that a suitable dosage will be obtained in any given unit dose of the compound. Factors, such as solubility, bioavailability, biological half-life, route of administration, product shelf life, as well as other pharmacological considerations, will be contemplated by one skilled in the art of preparing such pharmaceutical formulations, and as such, a y of dosages and treatment regimens may be desirable.

In other non—limiting examples, a dose may also comprise from about 1 microgram/kg/body weight, about 5 microgram/kg/body , about 10 microgram/kg/body weight, about 50 microgram/kg/body , about 100 microgram/kg/body weight, about 200 microgram/kg/body weight, about 350 microgram/kg/body weight, about 500 microgram/kg/body weight, about 1 ram/kg/body , about 5 milligram/kg/body weight, about 10 milligram/kg/body , about 50 milligram/kg/body weight, about 100 milligram/kg/body weight, about 200 milligram/kg/body weight, about 350 milligram/kg/body weight, about 500 milligram/kg/body weight, to about 1000 milligram/kg/body weight or more per administration, and any range derivable therein. In non—limiting es of a derivable range from the numbers listed herein, a range of about 5 ram/kg/body weight to about 100 milligram/kg/body weight, about 5 microgram/kg/body weight to about 500 milligram/kg/body weight, etc, can be administered, based on the numbers described above.

X. Combination Treatments In certain embodiments, the compositions and methods of the present embodiments involve administration of a kynureninase in ation with a second or onal therapy. Such therapy can be applied in the treatment of any disease that is associated with kynurenine dependency. For example, the disease may be cancer.

The methods and compositions, including combination therapies, e the therapeutic or tive effect, and/or increase the therapeutic effect of another anti-cancer or anti-hyperproliferative therapy. Therapeutic and prophylactic methods and compositions can be provided in a combined amount effective to achieve the desired effect, such as the killing of a cancer cell and/or the inhibition of cellular hyperproliferation. This -3 8- process may e administering a kynureninase and a second therapy. The second therapy may or may not have a direct cytotoxic effect. For example, the second therapy may be an agent that upregulates the immune system without having a direct cytotoxic effect. A tissue, tumor, or cell can be exposed to one or more compositions or pharmacological formulation(s) comprising one or more of the agents (e.g., a kynureninase or an anti-cancer agent), or by exposing the tissue, tumor, and/or cell with two or more ct compositions or formulations, n one composition provides 1) a kynureninase, 2) an anti-cancer agent, or 3) both a kynureninase and an ancer agent. Also, it is contemplated that such a combination therapy can be used in conjunction with chemotherapy, radiotherapy, al therapy, or immunotherapy.

The terms “contacted” and “exposed,” when applied to a cell, are used herein to describe the process by which a eutic construct and a chemotherapeutic or radiotherapeutic agent are delivered to a target cell or are placed in direct juxtaposition with the target cell. To achieve cell killing, for example, both agents are delivered to a cell in a combined amount ive to kill the cell or prevent it from dividing.

A kynureninase may be administered before, during, after, or in various combinations relative to an anti-cancer treatment. The administrations may be in intervals ranging from concurrently to minutes to days to weeks. In embodiments where the ninase is provided to a patient separately from an ancer agent, one would generally ensure that a significant period of time did not expire between the time of each delivery, such that the two compounds would still be able to exert an advantageously combined effect on the patient. In such instances, it is plated that one may provide a patient with the kynureninase and the ancer therapy within about 12 to 24 or 72 h of each other and, more particularly, within about 6—12 h of each other. In some situations it may be desirable to extend the time period for treatment significantly where several days (2, 3, 4, 5, 6, or 7) to several weeks (1, 2, 3, 4, 5, 6, 7, or 8) lapse n respective administrations.

In certain embodiments, a course of treatment will last 1-90 days or more (this such range includes intervening days). It is contemplated that one agent may be given on any day of day l to day 90 (this such range es intervening days) or any combination thereof, and another agent is given on any day of day 1 to day 90 (this such range includes intervening days) or any combination thereof. Within a single day (24—hour period), the patient may be given one or multiple administrations of the agent(s). Moreover, after a course of treatment, it is contemplated that there is a period of time at which no ancer treatment is administered. This time period may last 1-7 days, and/or 1-5 weeks, and/or 1—12 months or more (this such range es intervening days), ing on the condition of the t, such as their prognosis, strength, health, etc. It is expected that the treatment cycles would be repeated as necessary.

Various ations may be employed. For the example below a kynureninase is “A” and an anti-cancer therapy is “B”: A/B/A B/A/B B/B/A A/A/B A/B/B B/A/A A/B/B/B B/A/B/B B/B/B/A B/B/A/B A/A/B/B A/B/A/B A B/B/A/A B/A/B/A B/A/A/B A/A/A/B B/A/A/A A/B/A/A A ] Administration of any compound or y of the present embodiments to a patient will follow general protocols for the administration of such compounds, taking into account the toxicity, if any, of the agents. Therefore, in some embodiments there is a step of ring toxicity that is attributable to combination therapy.

A. Chemotherapy A wide variety of chemotherapeutic agents may be used in accordance with the present embodiments. The term therapy” refers to the use of drugs to treat cancer. A “chemotherapeutic agent” is used to connote a compound or composition that is administered in the treatment of cancer. These agents or drugs are categorized by their mode of activity within a cell, for example, whether and at what stage they affect the cell cycle.

Alternatively, an agent may be characterized based on its ability to directly cross-link DNA, to alate into DNA, or to induce chromosomal and mitotic aberrations by affecting nucleic acid synthesis.

[00156] Examples of chemotherapeutic agents include alkylating agents, such as thiotepa and cyclosphosphamide; alkyl sulfonates, such as busulfan, improsulfan, and piposulfan; aziridines, such as benzodopa, carboquone, meturedopa, and uredopa; ethylenimines and methylamelamines, including altretamine, triethylenemelamine, trietylenephosphoramide, triethiylenethiophosphoramide, and trimethylolomelamine; enins (especially bullatacin and bullatacinone); a camptothecin (including the synthetic analogue topotecan); bryostatin; callystatin; CC—1065 (including its adozelesin, carzelesin and bizelesin synthetic ues); cryptophycins (particularly cryptophycin l and cryptophycin 8); atin; duocarmycin ding the synthetic analogues, KW—2189 and CBl-TMl); eleutherobin; pancratistatin; a sarcodictyin; spongistatin; nitrogen mustards, such as chlorambucil, chlomaphazine, cholophosphamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, ichin, phenesterine, prednimustine, trofosfamide, and uracil d; ureas, such as carmustine, chlorozotocin, fotemustine, lomustine, nimustine, and ranimnustine; otics, such as the enediyne antibiotics (e.g., calicheamicin, especially eamicin gammalI and calicheamicin omegaIl); dynemicin, ing cin A; bisphosphonates, such as clodronate; an esperamicin; as well as neocarzinostatin chromophore and related chromoprotein enediyne iotic chromophores, aclacinomysins, actinomycin, authrarnycin, azaserine, bleomycins, cactinomycin, carabicin, carminomycin, carzinophilin, chromomycinis, dactinomycin, daunorubicin, detorubicin, 6—diazo—5—oxo—L—norleucine, doxorubicin ding morpholino-doxorubicin, cyanomorpholino—doxorubicin, 2-pyrrolino- bicin and oxorubicin), epirubicin, esorubicin, idarubicin, marcellomycin, mitomycins, such as mitomycin C, mycophenolic acid, nogalarnycin, olivomycins, peplomycin, potfiromycin, puromycin, quelamycin, rodorubicin, streptonigrin, streptozocin, tubercidin, ubenimex, atin, and zorubicin; anti—metabolites, such as methotrexate and 5— fluorouracil (5—FU); folic acid analogues, such as denopterin, terin, and trimetrexate; purine analogs, such as fludarabine, 6—mercaptopurine, thiamiprine, and thioguanine; pyrimidine analogs, such as ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, dideoxyuridine, ridine, enocitabine, and floxuridine; androgens, such as calusterone, dromostanolone propionate, epitiostanol, mepitiostane, and testolactone; anti-adrenals, such as mitotane and trilostane; folic acid replenisher, such as frolinic acid; aceglatone; aldophosphamide glycoside; aminolevulinic acid; eniluracil; amsacrine; bucil; bisantrene; edatraxate; defofamine; demecolcine; diaziquone; elformithine; elliptinium acetate; an epothilone; etoglucid; gallium nitrate; hydroxyurea; lentinan; lonidainine; maytansinoids, such as maytansine and ansamitocins; mitoguazone; mitoxantrone; mopidanmol; nitraerine; pentostatin; phenamet; pirarubicin; losoxantrone; podophyllinic acid; 2-ethylhydrazide; procarbazine; PSKpolysaccharide complex; razoxane; rhizoxin; sizofiran; spirogermanium; tenuazonic acid; triaziquone; 2,2',2"-trichlorotriethylamine; trichothecenes ially T-2 toxin, urin A, roridin A and anguidine); urethan; Vindesine; dacarbazine; mannomustine; mitobronitol; mitolactol; pipobroman; gacytosine; arabinoside (“Ara-C”); cyclophosphamide; s, e.g., paclitaxel and docetaxel gemcitabine; 6-thioguanine; mercaptopurine; platinum coordination complexes, such as cisplatin, oxaliplatin, and carboplatin; vinblastine; um; etoposide (VP-16); ifosfamide; mitoxantrone; vincristine; vinorelbine; rone; teniposide; edatrexate; daunomycin; aminopterin; xeloda; ibandronate; irinotecan (e.g., CPT-ll); omerase inhibitor RFS 2000; difluorometlhylornithine (DMFO); retinoids, such as retinoic acid; capecitabine; carboplatin, procarbazine,plicomycin, gemcitabien, navelbine, farnesyl-protein tansferase inhibitors, transplatinum, and pharmaceutically acceptable salts, acids, or derivatives of any of the above.

B. Radiotherapy ] Other factors that cause DNA damage and have been used extensively include what are commonly known as y—rays, X—rays, and/or the directed delivery of radioisotopes to tumor cells. Other forms of DNA damaging factors are also contemplated, such as microwaves, proton beam irradiation (US. Patents 5,760,395 and 4,870,287), and UV-irradiation. It is most likely that all of these factors affect a broad range of damage on DNA, on the sors of DNA, on the replication and repair of DNA, and on the assembly and maintenance of chromosomes. Dosage ranges for X—rays range from daily doses of 50 to 200 roentgens for prolonged periods of time (3 to 4 wk), to single doses of 2000 to 6000 roentgens. Dosage ranges for sotopes vary widely, and depend on the half—life of the isotope, the strength and type of radiation emitted, and the uptake by the neoplastic cells.

C. Immunotherapy The skilled n will understand that immunotherapies may be used in combination or in conjunction with methods of the ments. In the context of cancer treatment, immunotherapeutics, generally, rely on the use of immune effector cells and molecules to target and destroy cancer cells. Rituximab (RITUXAN®) is such an example.

Checkpoint inhibitors, such as, for e, ipilumimab, are another such example. The immune effector may be, for example, an antibody specific for some marker on the surface of a tumor cell. The antibody alone may serve as an effector of y or it may recruit other cells to actually affect cell killing. The antibody also may be conjugated to a drug or toxin (chemotherapeutic, radionuclide, ricin A chain, cholera toxin, pertussis toxin, etc.) and serve merely as a targeting agent. Alternatively, the effector may be a lymphocyte carrying a surface molecule that interacts, either directly or indirectly, with a tumor cell target. Various effector cells include cytotoxic T cells and NK cells.

In one aspect of immunotherapy, the tumor cell must bear some marker that is amenable to targeting, z'.e., is not present on the majority of other cells. Many tumor markers exist and any of these may be suitable for targeting in the t of the present embodiments. Common tumor markers include CD20, carcinoembryonic n, tyrosinase (p97), gp68, TAG—72, HMFG, Sialyl Lewis Antigen, MucA, MucB, PLAP, laminin receptor, erb B, and p155. An alternative aspect of immunotherapy is to combine ncer effects with immune stimulatory s. Immune stimulating molecules also exist including: cytokines, such as IL-2, IL-4, IL-12, GM-CSF, gamma-IFN, chemokines, such as MIP—l, MCP-l, IL—8, and growth factors, such as FLT3 .

Examples of therapies currently under investigation or in use are immune adjuvants, e.g., Mycobacterium bovis, Plasmodium falcz'parum, dinitrochlorobenzene, and aromatic compounds (US. Patents 5,801,005 and 5,739,169; Hui and oto, 1998; Christodoulides et al., 1998); ne therapy, e.g., interferons 0t, [3, and y, IL—l, GM-CSF, and TNF (Bukowski et al, 1998; Davidson et al, 1998; Hellstrand et al., 1998); gene therapy, e. g., TNF, IL—1, IL—2, and p53 (Qin et al., 1998; —Ward and Villaseca, 1998; US. Patents 5,830,880 and 5,846,945); and monoclonal antibodies, e.g., anti-CD20, anti-ganglioside GM2, and anti-p185 (Hollander, 2012; Hanibuchi et al., 1998; US. Patent 5,824,311). It is contemplated that one or more anti-cancer therapies may be employed with the antibody therapies described herein.

D. Surgery ] Approximately 60% of persons with cancer will undergo surgery of some type, which includes preventative, diagnostic or staging, ve, and palliative surgery. Curative surgery includes resection in which all or part of cancerous tissue is physically removed, excised, and/or destroyed and may be used in conjunction with other therapies, such as the treatment of the present embodiments, chemotherapy, radiotherapy, hormonal therapy, gene therapy, therapy, and/or ative therapies. Tumor resection refers to physical removal of at least part of a tumor. In addition to tumor resection, treatment by surgery includes laser surgery, cryosurgery, electrosurgery, and microscopically—controlled surgery (Mohs’ surgery). 2014/053437 Upon excision of part or all of cancerous cells, tissue, or tumor, a cavity may be formed in the body. Treatment may be accomplished by perfusion, direct injection, or local application of the area with an onal anti-cancer therapy. Such treatment may be repeated, for example, every 1, 2, 3, 4, 5, 6, or 7 days, or every 1, 2, 3, 4, and 5 weeks or every 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 months. These treatments may be of varying dosages as well.

E. Other Agents It is contemplated that other agents may be used in combination with certain aspects of the present embodiments to improve the therapeutic efficacy of ent.

These additional agents include agents that affect the upregulation of cell surface receptors and GAP junctions, cytostatic and differentiation agents, inhibitors of cell adhesion, agents that increase the sensitivity of the hyperproliferative cells to apoptotic inducers, or other biological agents. ses in intercellular signaling by elevating the number of GAP junctions would increase the anti-hyperproliferative effects on the oring hyperproliferative cell population. In other embodiments, cytostatic or differentiation agents can be used in combination with certain aspects of the present ments to improve the anti-hyperproliferative efficacy of the treatments. Inhibitors of cell adhesion are plated to improve the efficacy of the present embodiments. Examples of cell adhesion inhibitors are focal on kinase (FAKs) inhibitors and Lovastatin. It is further contemplated that other agents that increase the sensitivity of a hyperproliferative cell to apoptosis, such as the antibody c225, could be used in combination with certain aspects of the present embodiments to improve the treatment efficacy.

XI. Kits Certain aspects of the present ion may provide kits, such as therapeutic kits. For example, a kit may comprise one or more pharmaceutical composition as described herein and optionally instructions for their use. Kits may also comprise one or more devices for lishing administration of such compositions. For example, a subject kit may comprise a ceutical composition and catheter for accomplishing direct intravenous ion of the composition into a cancerous tumor. In other embodiments, a subject kit may comprise lled ampoules of a kynureninase, optionally formulated as a pharmaceutical, or lyophilized, for use with a delivery device.

Kits may comprise a container with a label. le containers include, for example, s, vials, and test tubes. The containers may be formed from a variety of als, such as glass or plastic. The container may hold a composition that includes a kynureninase that is effective for therapeutic or non-therapeutic applications, such as described above. The label on the container may indicate that the composition is used for a specific therapy or non-therapeutic application, and may also indicate directions for either in vivo or in vitro use, such as those described above. The kit of the invention will typically comprise the container bed above and one or more other containers comprising materials desirable from a cial and user standpoint, ing buffers, diluents, filters, needles, syringes, and package inserts with instructions for use.

XII. Examples The following examples are ed to demonstrate preferred embodiments of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent ques discovered by the inventor to function well in the practice of the invention, and thus can be considered to tute preferred modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.

Example 1 — Gene construction, expression, and purification of kynureninase from Psuedomonasfluorescens A gene for expression of the kynureninase enzyme from monas fluorescens (Pf—KYNU) was constructed by overlap extension rase chain reaction (PCR) of four codon optimized gene blocks designed using DNA—Works software (Hoover and Lubkowski, 2002). The full-length gene includes an N—terminal Xbal restriction enzyme site (nucleotides 1—6), an optimized ribosome g site (RBS; nucleotides 29—55), a start codon (nucleotides 56—58), an N—terminal His6 tag otides 59—91), an E. coli codon optimized Pf—KYNU gene (nucleotides 92—1336), a stop codon (nucleotides 1337—1342), and a C—terminal BamHI restriction enzyme site (nucleotides 1342—1347) (see, SEQ ID NO: 1).

The aforementioned restriction enzyme sites were used to clone the assembled gene into a pET—28a+ vector (Novagen). This construct was then used to transform BL21 (DE3) E. coli for expression. Cells were grown at 37 °C with shaking at 210 rpm in Terrific Broth (TB) media with 50 mg/L of kanamycin. Expression was d when an OD600 ~1.0 was reached by adding IPTG (0.5 mM final concentration) with continued shaking overnight at 37 °C. Cells were then harvested by fugation and re—suspended in lysis buffer consisting of 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, 0.5 mM pyridoxyl phosphate (PLP), 1 mM phenylmethylsulfonylfluoride, and 1 ug/mL DNase. Lysis was achieved by French press and the lysate was cleared of particulates by centrifuging at 20,000 x g for 1 h at 4 0C. The atant was then filtered through a 5 pm syringe filter and d to a Ni-NTA/agarose column (Qiagen) pre—equilibrated in a buffer composed of 50 mM sodium phosphate, 300 mM NaCl, and 0.1 mM PLP at pH 7.4. After loading the lysate onto the column, the resin was washed with 5 column volumes (CV) of 50 mM sodium ate, pH 7.4, 300 mM NaCl, and 0.1 mM PLP with 30 mM imidazole. Next, the flow rate was set to slowly wash the column overnight with 100 CV of endotoxin-free PBS (Corning) buffer with 0.1 mM PLP and 1% v/v TRITON® X114. This overnight wash removes lipopolysaccharide (LPS or endotoxin) that is a typical contaminant of bacterial expression systems. The washed enzyme was then eluted in 5 CV of endotoxin—free PBS with 0.1 mM PLP with 250 mM imidazole, and the resin was rinsed with a second 5 CV portion of endotoxin free PBS with 0.1 mM PLP. At this point, enzyme was buffer exchanged into fresh PBS to remove imidazole, 10% glycerol was added and aliquots were flash frozen in liquid nitrogen for storage at -80 °C.

Alternatively, enzyme was immediately buffer exchanged into freshly made, sterile 100 mM sodium phosphate, pH 8.4, to both remove ole and prepare it for tion (see, Example 4). Enzyme purities were typically >95% based on SDS-PAGE is and typical yields averaged around 75 mg/L of culture. Protein quantities were assessed by measuring nm and using the calculated enzyme extinction coefficient of 63,745 M'lcm'l.

Example 2 — Gene construction, expression, and purification of kynureninase from Homo s A gene for expression of the ninase enzyme from Homo sapiens (h-KYNU) was obtained by overlap extension polymerase chain reaction (PCR) of four codon optimized gene blocks designed using DNA—Works software (Hoover and Lubkowski, 2002). The full-length gene includes an N—terminal Xbal restriction enzyme site (nucleotides 1—6), an optimized RBS (nucleotides 28-60), a start codon (nucleotides 61-63), an N—terminal His6 tag (nucleotides 64—96), an E. coli codon optimized h—KYNU gene (nucleotides 97— 1488), a stop codon (nucleotides 1489—1491), and a C—terminal BamHI restriction enzyme site otides 1492—1497) (see, SEQ ID NO: 2). The aforementioned restriction enzyme sites were used to clone the assembled gene into a pET-28a+ vector (Novagen). This construct was then used to transform BL21 (DE3) E. coli for expression. Cells were grown at 37 0C with g at 210 rpm in Terrific Broth (TB) media with 50 mg/L of kanamycin.

Expression was induced when an OD500 ~l.0 was reached by adding IPTG (0.5 mM final concentration) with ued shaking overnight at 37 0C. Cells were then harvested by centrifugation and re-suspended in lysis buffer consisting of 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, 0.5 mM pyridoxyl phosphate (PLP), 1 mM phenylmethylsulfonylfluoride, and 1 ug/mL DNase. Lysis was achieved by French press and the lysate was cleared of particulates by fuging at 20,000 x g for l h at 4 °C. The atant was then filtered through a 5 pm syringe filter and applied to a Ni-NTA/agarose column (Qiagen) pre-equilibrated in 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, and 0.1 mM PLP buffer. After loading the lysate onto the , the resin was washed with 5 column volumes (CV) of 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, and 0.1 mM PLP with 30 mM imidazole. Next, the flow rate was set to slowly wash the column overnight with 100 CV of endotoxin-free PBS (Corning) buffer with 0.1 mM PLP and 1% v/v TRITON® X114. This overnight wash removes lipopolysaccharide (LPS or endotoxin) that is a l contaminant in bacterial expression of enzymes. The washed enzyme was then eluted in 5 CV of endotoxin free PBS with 0.1 mM PLP with 250 mM imidazole and the resin was rinsed with a second 5 CV portions of endotoxin free PBS with 0.1 mM PLP. At this point, enzyme was buffer exchanged into fresh PBS to remove imidazole, 10% glycerol was added and aliquots were flash frozen in liquid nitrogen for storage at -80 0C. atively, enzyme could be buffer exchanged into freshly made, sterile 100 mM sodium phosphate, pH 8.4, to both remove imidazole and prepare it for PEGylation (see, Example 4).

Enzyme purities were typically >95% as assessed by SDS—PAGE is and typical yields ed around 20 mg/L of liquid culture. Protein quantities were assessed by measuring AbSZgonm and using the calculated enzyme extinction coefficient of 76,040 M'lcm'l.

Example 3 — Gene construction, expression, and purification of kynureninase from Mus musculus A gene for expression of the kynureninase enzyme from Mus musculus (m—KYNU) was obtained by overlap extension polymerase chain reaction (PCR) of three WO 31771 codon optimized gene blocks designed using DNA—Works software (Hoover et (21., 2002).

The full-length gene included an N—terminal XbaI restriction enzyme site (nucleotides 1-6), an zed RBS otides 29-58), a start codon (nucleotides 59—61), an N—terminal His6 tag (nucleotides 62—94), an E. coli codon optimized m—KYNU gene otides 95—1483), a stop codon (nucleotides 486), and a inal BamHI restriction enzyme site (nucleotides 1487—1492) (see, SEQ ID NO: 3). The aforementioned restriction enzyme sites were used to clone the assembled gene into a pET-28a+ vector (Novagen). This construct was then used to transform BL21 (DE3) E. 0012' for expression. Cells were grown at 37 0C shaking at 210 rpm in Terrific Broth (TB) media with 50 mg/L of kanamycin. Expression was induced when an OD600 ~1.0 was reached by adding 0.5 mM IPTG and continued overnight at 37 0C. Cells were harvested by centrifugation and re—suspended in lysis buffer consisting of 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, 0.5 mM pyridoxyl phosphate (PLP), 1 mM phenylmethylsulfonylfluoride, and 1 ug/mL DNase. Lysis was ed by French press and the lysate cleared of particulates by centrifuging at 20,000 x g for 1 h at 4 °C. The supernatant was filtered through a 5 um syringe filter and applied to a Ni- NTA/agarose column n) pre—equilibrated in 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, and 0.1 mM PLP buffer. After loading the lysate onto the column, the resin was washed with 5 column volumes (CV) of 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, and 0.1 mM PLP with 30 mM imidazole. Next the flow rate was set to slowly wash overnight with 100 CV of xin-free PBS (Corning) buffer with 0.1 mM PLP and 1% v/v TRITON® X114. This overnight wash removeD lipopolysaccharide (LPS or endotoxin) that is a typical contaminant in bacterial expression of enzymes. The washed enzyme was eluted in 5 CV of endotoxin-free PBS with 0.1 mM PLP with 250 mM imidazole and the resin rinsed with a second 5 CV portion of endotoxin—free PBS with 0.1 mM PLP. At this point, enzyme was buffer exchanged into fresh PBS to remove imidazole, 10% glycerol added and aliquots flash frozen in liquid nitrogen for e at —80 0C.

Example 4 — cological preparation of kynureninase from Pseudomonas fluorescens To improve the circulation time of the enzyme in vivo, the hydrodynamic radius of KYNU enzymes was increased by functionalizing surface ve groups in the protein by conjugation to PEG. In one embodiment, Pf—KYNU was functionalized by reaction of surface lysine residues with Methoxyl PEG Succinimidyl Carbonate 5000 MW (NANOCS). The purified, endotoxin—free enzyme was thoroughly buffer exchanged into y prepared 100 mM sodium phosphate, pH 8.4, and concentrated to 10 mg/mL. The resulting solution was added directly to a 100:1 molar excess of solid PEG reagent and d to react at room temperature for l h (. Un—reacted PEG was removed from solution by thorough buffer exchange into fresh, endotoxin—free PBS in a 100 kDa cut off centrifugal filtration device (AMICON®). The nt molecular mass of the enzyme was then checked on a size exclusion HPLC column (Phenomenex) in PBS. A MW standard solution from BioRad was used to te a standard curve and enzyme retention times compared to those of the protein standards. Based on the standard curve, the non- PEGylated enzyme has an apparent mass of 40 kDa, which is close to that of the mass of one monomer of Pf—KYNU. The PEGylated version of the enzyme was seen to have an apparent mass of 1,300 kDa, i.e. substantially larger than the unmodified enzyme. Endotoxin levels were quantified using the Chromo-LAL c chromogenic endotoxin testing kit (Associates of Cape Cod, Inc.). Enzyme washed in the manner described above typically resulted in endotoxin levels 0.19 i 0.07 EU/mg of purified U.

Example 5 — Pharmacological preparation of kynureninase from Homo sapiens To improve circulatory residence time of the human enzyme in vivo, the hydrodynamic radius of h-KYNU was increased by functionalizing surface reactive groups in the protein by conjugation to PEG. In one embodiment, h—KYNU was functionalized by on of surface lysine es with Methoxyl PEG Succinimidyl ate 5000 MW (NANOCS). The purified, endotoxin—free enzyme was thoroughly buffer exchanged into freshly ed 100 mM sodium phosphate, pH 8.4, and concentrated to 10 mg/mL. The resulting solution was added directly to a 100:1 molar excess of solid PEG reagent and allowed to react at room temperature for l h. Un—reacted PEG was removed from solution by thorough buffer ge into fresh, endotoxin-free PBS in a 100 kDa cut off centrifugal filtration device (AMICON®). The apparent molecular mass of the enzyme was determined using a size ion HPLC column (Phenomenex) equilibrated with PBS and retention times compared to a MW standard solution (BioRad). Endotoxin levels were quantified using the Chromo-LAL kinetic chromogenic endotoxin testing kit (Associates of Cape Cod, Inc.).

Example 6 — Assay for measuring kinetic parameters of kynureninase The kinetic parameters of Pf-KYNU and h—KYNU, as well as of their PEGylated versions as described in Examples 4 and 5, were quantified by a spectrophotometric assay, in which the decay in the maximum absorbance of the enzyme substrate, L-kynurenine, was monitored as a function of time. renine solutions were prepared in a PBS buffer, pH 7.4, to result in final concentrations ranging from 8 “M to 250 “M. L-Kynurenine has an extinction coefficient of 4,500 M'lcm'1 with a 7mm at 365 nm while the products of the kynureninase reaction, L-anthranilic acid and L-alanine, do not appreciably absorb at 365 nm. Reactions were initiated by adding and rapidly mixing enzyme solutions (~20 nM final) with the substrate solutions and ring the loss of substrate KYN at 25 °C by measuring Abs365 um over time. The resulting data was sed and fitted to the Michaelis-Menten equation for determining kinetic constants. The kinetics of PEGylated Pf—KYNU enzyme was measured in an identical manner. For the non— PEGylated enzyme, kcat/KM = 1.0 X 105 M'ls'l, and for the PEGylated form, kcat/KM = 1.3 X 105 M'ls‘l. c parameters for the hydrolysis of 3-hydroxy-L-kynurenic acid were also determined as bed here.

Example 7 - In vitro stability of ninase To measure the in vitro stability of Pf—KYNU, the enzyme was added to either PBS buffer or pooled human serum to a final concentration of 10 uM and incubated at 37 °C. Portions of 10 ”L each were taken out at time points and added to 990 ML of a 250 “M on of L—kynurenine/PBS. The initial rate of reaction was monitored by ing the decay of absorbance at 365 nm over time as described in Example 3. Enzyme stability was determined by comparing the initial rate of renine catalysis at each time point and comparing it to the rate at time = 0. The resulting data was plotted as % activity vs. time and fitted to an exponential equation to determine the half-life (Tl/2). The Pf-KYNU enzyme was found to have a Tm = 34.3 hours in PBS and a Tm = 2.4 hours in pooled human serum (FIG. e 8 — Assay for quantifying nine and tryptophan levels in vivo In vivo levels of L-kynurenine, tryptophan, kynureninic acid, 3- hydroxy—L-kynurenine and L-anthranlilic acid (one of the products of kynureninase catalysis) were quantified and monitored by HPLC. Upon necropsy of the mice, samples of blood, the tumor, the spleen, and the liver were removed. Blood samples were centrifuged to separate whole blood from serum. Tissue samples were first homogenized, and then centrifuged to remove the solid portion. To each liquid portion was added a 1:10 v/v portion of 100% trichloroacetic acid to precipitate macromolecules. Solids were again removed by centrifuging and the supernatants were passed through a 0.45 um syringe filter. The treated supernatants were d ly to a HPLC dzu) and separated on a standard analytical C-l8 column using a gradient starting from 0% solution B to 100% solution B where solution A is H20 + 0.1% trifluoroacetic acid and on B is acetonitrile + 0.1% trifluoroacetic acid. The full absorbance range from 190 nm to 900 nm was continually collected to monitor all possible molecules and fluorescence spectroscopy (Ex = 365 nm, Em = 480 nm) was simultaneously collected to specifically monitor kynurenine levels.

Concentrations and retention times were determined using standard solutions made from the pure molecules (Sigma).

Example 9 — Efficacy of PEG-Pf—KYNU in the autologous B16 mouse melanoma model

[00175] B6—WT mice (n = 20) were each inoculated with 2.5 >< 105 B16 murine melanoma cells by subcutaneous flank injection. After ng tumors to establish for 10 days (tumor mean = 20 mm2) the mice were split into two groups of n = 10 each. The l group was then treated with 20 mg/kg of heat inactivated PEG-Pf—KYNU by intra—tumoral injection every three days until tumors reached 350 mm2 in size. The experimental group was treated in an identical manner except with 20 mg/kg of active PEG-Pf—KYNU by intra- tumoral injection every three days until tumors reached an endpoint of 350 mm2 in size. The growth rates of B16 melanoma tumors was significantly retarded in the treatment group administered active PEG—Pf—KYNU compared to the identically treated heat-inactivated PEG-Pf—KYNU group ( resulting in a significant life—span extension (.

Lymphocytes ed from control and experimental treatment groups were assessed with panels of dies (z'.e., anti-CD45, CD4, Nkl.l, CD25, FoxP3, CD8, granzyme B, IFNy, CTLA4, CDllc, CDllb, F4/80, GR—l, and Ly6—C) which revealed that the population of ating CD4+ CD25+ FoxP3+ regulatory T-cells was cantly lower in the group treated with active PEG—Pf—KYNU (4.8 i 0.8% vs. 8.6 i 0.8%). In addition, the population of tumor infiltrating CD8+ T-cells expressing granzyme B and interferon y was significantly higher in mice treated with active enzyme (26 :: 19% vs. 4 i 2%) (FIGS. 5A—B).

Example 10 — Kynureninase—scFv fusion proteins for tumor targeting In some aspects, the present invention also contemplates polypeptides comprising the modified bacterial or mammalian kynureninase linked to a heterologous amino acid sequence. For example, the native or modified ninase may be linked to a single-chain variable fragment (scFv) antibody that binds specific cell surface tumor antigens.

In this embodiment an scFv-kynureninase fiision protein with the scFv portion of the protein having specific affinity for a known tumor antigen, preferably a tumor specific antigen that intemalizes at a slower rate, e. g., MUC-l, would allow the kynureninase portion of the fusion protein to be delivered to the tumor cell and degrade KYN. One example would be a scFv— kynureninase fusion protein where the scFv portion targets and binds to the human epidermal growth factor receptor 2 (HERZ) that is upregulated in certain types of breast cancer.

In this embodiment a native or modified kynureninase-anti-HERZ- scFV fusion protein would act to target and concentrate kynureninase directly to the tumor surface and act to degrade tumor—produced KYN. e 11 — ninase-anti—CTLA4-scFV fusion proteins In some aspects, the present invention also contemplates polypeptides comprising the modified bacterial or mammalian kynureninase linked to a heterologous amino acid ce. For e, the native or modified kynureninase may be linked to a single-chain le nt (scFv) antibody that binds the Cytotoxic T—Lymphocyte Antigen 4 4) receptor, mmed Cell Death 1 (PD-l), or Programmed Cell Death Ligand l (PD-Ll). A blockade of CTLA—4, PD—l, or PD—Ll by an antagonizing antibody or antibody fragment allows the inhibitory T-cell signal to be reversed allowing CD28 to stimulate T-cell activation. In this embodiment a native or modified kynureninase-anti- CTLA4-, anti-PD—l-, or anti-PD-Ll-scFv fusion protein would act to remove both inhibitory proteinzprotein interaction ing and inhibitory kynurenine signaling. This embodiment of a native or d kynureninase—scFv fusion protein would be expected to ly upregulate T—cell activation and e robust anti—tumoral responses.

WO 31771 Example 12 — Chimeric antigen receptor constructs for delivery of kynureninase to T cells In some aspects, the present invention also contemplates a lentiviral vector suitable for transfection of T cells with chimeric n receptor (CAR) constructs such that a modified bacterial or mammalian kynureninase would be co-expressed in addition to the CAR construct. CAR constructs are proteins containing an extracellular antigen binding domain fused to a transmembrane and cytoplasmic signaling domain from a CD31, chain and often a CD28 molecule (Ahmed et al., 2010). The antigen binding domain may be an scFv designed to bind an antigen expressed by a tumor cell with es being HER2 expressed by glioblastoma or osteosarcoma, CD19 or CD20 expressed by various B—cell malignancies, or GD2 expressed by neuroblastoma (Lipowska-Bhalla er al., 2012) or any other relevant target. In this embodiment the lentiviral vector, delivering an appropriate CAR construct to a T cell, would in addition co-express a native or modified bacterial or mammalian kynureninase in the cytosol. The T cell containing this CAleynureninase construct would have the dual ability to 1) bind to specific tumor cells and 2) to degrade KYN, preventing KYN induction of a tory phenotype and or apoptosis. In another ment a T cell would express a CAR uct that binds a CD19+ or CD20+ diffuse large B-cell lymphoma while co-expressing a kynureninase to degrade the high concentrations of KYN often produced by this tumor type (Yoshikawa et ai, 2010; de Jong et al., 2011; Yao et al., 2011).

Example 13 — Genetic selection for kynureninase ty The amino acid L-tryptophan (L-Trp) is synthesized from the e derived precursor, chorismate, by sion of the trp biosynthetic genes. In ia such as E. 6011' the trp thetic genes are organized in an operon composed of five genes; trpE, trpD, trpC, trpB, and trpA. The TrpE and TrpD proteins are components of the anthranilate synthase complex that catalyzes the first step in the sion of chorismate and L- glutamine to nilic acid and L-glutamate. Anthranilic acid is then subsequently converted to L—Trp by the action of TrpC, TrpA, and TrpB. Cells g a functional anthranilate synthase gene are auxotrophic for L-Trp and cannot grow in minimal media without tryptophan. The inventors postulated that since kynurenine can be transported into the cytosol of many organisms, cells expressing recombinant L-kynureninase enzymes displaying a sufficiently high catalytic activity should be able to convert cytosolic L— 2014/053437 kynurenine to anthranilic acid and the latter then enables the synthesis of L—Trp. By contrast, cells that do not express the enzyme or express variants with low catalytic activity should display either no growth or very slow growth, respectively, on minimal media with L- kynurenine.

E. coli trpE and trpD deletion mutants were obtained from Genetic Resources at Yale CGSC. Strain pes were (F-,A(araD-araB)567, AlacZ4787(::rmB—3), 2v, AtrpE772::kan, rph—l, A(rhaD-rhaB)568, hst514) and (F-, A(araD—araB)567, AlacZ4787(::rrnB—3),?t-,AtrpD77l::kan, rph-l, A(rhaD-rhaB)568, hst514), respectively.

Cells were plated on M9 minimal media plates. Filter paper disks soaked in either L-Trp, L— Kyn, anthranilic acid, or buffer were then placed on the plates followed by incubation at 37 0C. E. coZi-AtrpD cells only grew in the presence of L-Trp, however E. coii-AtrpE could also grow in the presence of anthranilic acid but not buffer or L-Kyn, demonstrating that trpC, trpA, and trpB were expressed, ng rescue of the L-Trp ophy with anthranilic acid as an intermediate metabolite (. Furthermore, E. coli-AtrpE cells transformed with a plasmid harboring the Pf—KYNU gene grew ly on M9 minimal media plates in the presence of L—Kyn. e 14 — Gene construction, expression and ation of bacterial kynureninases ying high catalytic activity s kynurenine and identity to the human kynureninase

[00182] Similar to other eukaryotic kynureninases the Homo sapiens enzyme is highly selective towards the hydrolysis of 3’-OH kynurenine and has about 1,000-fold lower catalytic activity towards kynurenine. Because of its poor catalytic activity towards kynurenine, the human enzyme is not suitable for therapeutic purposes. Administration of PEGylated Pf—KYNU (Example 9), Mu-KYNU (Example 22 and Example 23), or Cp-KYNU (Example 17) (all of which display high catalytic activity towards kynurenine instead of 3’- OH kynurenine) resulted in tumor growth retardation as shown in Example 9 (.

However, stration of ted human ninase at r or higher dosing had no effect on the growth of B16 melanoma tumors (n = 4). However, as shown in Example , engineering of h-KYNU can improve the L-kynurenine degrading activity of the human enzyme. Such engineered h-KYNU variants may result in tumor growth retardation as seen with PEGylated Pf—KYNU (Example 9), Mu-KYNU (Example 22 and Example 23), and Cp- KYNU (Example 17).

] The Pf—KYNU displays low sequence identity to its human counterpart (24% amino acid identity). Due to its low sequence identity to the human protein, Pf-KYNU may elicit adverse immune responses in patients as well as the production of neutralizing antibodies. Therefore it is important to discover ninase enzymes that display high catalytic activity and selectivity towards kynurenine and have a higher degree of amino acid identity to the Homo sapiens kynureninase. The inventors identified a number of bacterial enzymes that display >3 8% amino acid identity to the Homo sapiens kynureninase and also high kynurenine hydrolysis activity. The sequences of these enzymes are provided as SEQ ID NOs: 13-52. The percent identities of these enzymes as compared to Homo sapiens kynureninase are provided in Table 1. As a entative e, a gene for expression of the kynureninase enzyme from Mucilaginibacter s (Mu-KYNU) (SEQ ID NO: 33) was constructed by overlap extension polymerase chain reaction (PCR) of two codon optimized gene blocks designed using the DNA—Works software (Hoover and Lubkowski, 2002). The full-length gene includes an inal Ncol restriction enzyme site, an optimized RBS, an N—terminal His6 tag, E. coli codon optimized Mu-KYNU gene, a stop codon and a C-terminal EcoRl restriction enzyme site. The aforementioned restriction enzyme sites were used to clone the assembled gene into a a+ vector (Novagen). This construct was then used to transform BL21 (DE3) E. coli for expression. Cells were grown at 37 0C with shaking at 210 rpm in Terrific Broth (TB) media with 50 mg/L of kanamycin. Expression was induced when an OD600 ~l.0 was reached by adding IPTG (0.5 mM final concentration) with ued shaking overnight at 37 °C. Cells were then harvested by fugation and re—suspended in lysis buffer consisting of 50 mM sodium ate, pH 7.4, 300 mM NaCl, 0.5 mM pyridoxyl ate (PLP), 1 mM phenylmethylsulfonylfluoride, and l ug/mL DNase. Lysis was achieved by French press and the lysate was cleared of particulates by fuging at 20,000 x g for 1 h at 4 °C. The supernatant was then filtered through a 5 mm syringe filter and applied to a Ni-NTA/agarose column n) pre-equilibrated in 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, and 0.1 mM PLP buffer. After loading the lysate onto the column, the resin was washed with 5 column s (CV) of 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, and 0.1 mM PLP with 30 mM imidazole. The washed enzyme was then eluted in 5 CV of PBS with 0.1 mM PLP with 250 mM imidazole. At this point, enzyme was buffer exchanged into fresh PBS to remove imidazole, 10% glycerol was added and aliquots were flash frozen in liquid nitrogen for storage at -80 °C. Enzyme purities were typically >95% based on SDS—PAGE analysis and typical yields averaged around 75 mg/L of culture. n quantities were assessed by measuring Aszgo mm and using the calculated enzyme extinction coefficient of 78,185 M'lcm'l.

Table 1. Percent identities of eubacterial kynureninase enzymes as compared to Homo sapiens kynureninase.

SEQ ID NO % Identit Arem'talea [urea 13 44.1 Belliella a DSM I5883 14 43.3 Bizionia argentinensis 15 42.9 Candidatus Entotkeonella Sp. TSYZ 16 44.9 Candidatus Koribacter versatilis Ellin345 17 43.3 Cecembia Zonarensz's 18 45.1 Chlam dmhila caviae GPIC 20 40.8 44.5 43-5 44.5 43-4 47 .5 45.7 47 .1 44.1 Kan; iella koreensis DSM 16069 30 44.3 Lacinutrix SI. 5H—3-7—4 31 44.2 mdz'us rol ticus 32 44.5 Mucilaginibacterpaludis 33 43 .9 Myroides adoratimimus 34 42.2 Myxococcusfulvus HW-I 35 44.5 Myxococcus stipitatus DSM 14675 36 44.4 M xococcus xanthus DK 1622 37 45.1 Niastella koreensis GR20-10 39 44.8 44.1 42.1 44.1 45.4 39.1 43.2 42.5 Xanthomonas axonopodis 48 42 Psychroflexus gondwanensis 49 44 lla cohaerens 50 45.6 44.9 Pontibacter roseus 52 44.8 Example 15 — Kinetic parameters of Mucilaginibacterpaludis kynureninase (Mu- KYNU) The kinetic parameters of Mu-KYNU were quantified by a spectrophotometric assay, in which the decay in the maximum absorbance of the enzyme substrate, L-kynurenine, was monitored as a function of time. L-Kynurenine solutions were prepared in a PBS buffer, pH 7.4, to result in final trations g from 16 [1M to 500 “M. L-Kynurenine has an extinction coefficient of 4,500 M'lcm'1 with a kmax at 365 nm while the products of the ninase reaction, L-anthranilic acid and ine, do not appreciably absorb at 365 nm. Reactions were initiated by adding and rapidly mixing enzyme solutions (~ 20 nM final concentration) with the substrate solutions and monitoring the loss of substrate at 25 °C by measuring Abs365 nm over time. The ing data were processed and fitted to the Michaelis-Menten equation for determining c constants.

Mu-KYNU was determined to have a Jew/KM = 1.2 x 105 .

Example 16 — In vitro stability of Mucilaginibacterpaludis kynureninase NU)

[00185] To measure the in vitro stability of Mu-KYNU, the enzyme was added to either PBS buffer or pooled human serum to a final concentration of 10 HM and incubated at 37 °C. Portions of 10 [LL each were taken out at time points and added to 990 [1L of a 250 [4M solution of L—kynurenine/PBS. The initial rate of reaction was monitored by measuring the decay of absorbance at 365 nm over time as described in Example 3. Enzyme stability was determined by comparing the initial rate of L-kynurenine catalysis at each time point and comparing it to the rate at time = 0. The resulting data were plotted as percent activity vs. time and fitted to a bi-phasic decay model (Stone et al., 2010) to determine the half—lives (Tl/2). The activity of U enzyme in PBS was found have a lTl/z = 6 h with an ude of 74% remaining activity and a subsequent 2Tm = 150 h (. The stability of Mu-KYNU enzyme in pooled human serum was determined to have a 1T1/2 = 5 h with an amplitude of 30% remaining activity and a subsequent 2T“; = 73 h (.

Example 17 — Gene uction, expression, and purification of kynureninase from Chlamydophila pecorum A gene for expression of the kynureninase enzyme from Chlamydophila pecorum (Cp—KYNU) was synthesized using E. coli—codon optimized gene blocks. The full-length gene includes an N—terminal NcoI restriction enzyme site (nucleotides 1—6), a start codon (nucleotides 3—5), an N—terminal His6 tag (nucleotides 6-35), an E. coli codon optimized Cp—KYNU gene (nucleotides 36—1295), a stop codon (nucleotides 1296— 1298), and a C-terminal EcoRl ction enzyme site otides 1299—1304) (SEQ ID NO: 53). The aforementioned restriction enzyme sites were used to clone the assembled gene into a pET-28a+ vector (Novagen). This construct was then used to transform BL21 (DE3) E. 0012' for expression. Cells were grown at 37 0C with shaking at 210 rpm in Terrific Broth (TB) media with 50 mg/L of kanamycin. Expression was d when an OD600 ~1.0 was reached by adding IPTG (0.5 mM final concentration) with continued shaking overnight at 16 0C. Cells were then harvested by fugation and re—suspended in lysis buffer consisting of 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, 0.5 mM pyridoxyl phosphate (PLP), 1 mM phenylmethylsulfonylfluoride, and 1 ug/mL DNase. Lysis was achieved by French press and the lysate was cleared of particulates by centrifuging at 20,000 x g for 1 h at 4 °C. The supernatant was then filtered h a 5 pm syringe filter and applied to a Ni-NTA/agarose column n) pre-equilibrated in 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, and 0.1 mM PLP buffer. After loading the lysate onto the column, the resin was washed with 10 column volumes (CV) of 50 mM sodium phosphate, pH 7.4, 300 mM NaCl, and 0.1 mM PLP with 30 mM ole. The washed enzyme was then eluted with 5 CV of PBS containing 0.1 mM PLP and 250 mM imidazole. The eluted enzyme was buffer exchanged into fresh PBS to remove ole, 10% glycerol was added, and aliquots were flash frozen in liquid nitrogen for e at —80 0C.

Example 18 — Kinetic parameters of Chlamydophila pecorum Kynureninase (Cp—KYNU) The kinetic parameters of Cp—KYNU (SEQ ID NO: 57) were quantified by a spectrophotometric assay, in which the decay in the maximum absorbance of the enzyme substrate, L-kynurenine, was monitored as a function of time. L-Kynurenine solutions were prepared in PBS buffer, pH 7.4, to result in final concentrations ranging from 16 MM to 500 uM. L-Kynurenine has an extinction coefficient of 4,500 M'lcm'1 with a 7mm at 365 nm while the products of the kynureninase reaction, anthranilate and L-alanine, do not iably absorb at 365 nm. Reactions were initiated by adding and rapidly mixing enzyme solutions (200 nM final concentrations) with the substrate solutions and monitoring the loss of substrate at 25 °C by measuring Abs365 um over time. The resulting data were —58- sed and fitted to the Michaelis-Menten equation for determining kinetic nts. Cp- KYNU was determined to have a kcat/KM = 3 X 104 M'ls'l.

Example 19 — cological preparation of kynureninase from Mucilaginibacter paludis To improve the circulation time of the enzyme in vivo, the hydrodynamic radius of Mu-KYNU was increased by functionalizing surface reactive groups in the protein by conjugation to PEG. In one embodiment, Mu—KYNU was PEGylated by reaction of surface lysine es with Methoxyl PEG Succinimidyl Carbonate 5000 MW (NANOCS). The purified Mu-KYNU, was determined to contain very low xin levels (<20 EU/mg) as bed below. It was thoroughly buffer exchanged into freshly prepared 100 mM sodium phosphate buffer, pH 8.4, and concentrated to greater than 1 mg/mL. The resultant solution was added directly to a 100:1 molar excess of solid PEG reagent and allowed to react at room temperature for l h with stirring. Un-reacted PEG was removed from solution by thorough buffer exchange into fresh, endotoxin—free PBS in a 100 kDa cutoff centrifugal filtration device n). The nt molecular mass of the enzyme was then checked on a size ion HPLC column (Phenomenex) in PBS using a MW standard solution from BioRad to generate a standard curve, and enzyme retention times were compared to those of the protein standards. Endotoxin levels were quantified using the Chromo—LAL kinetic chromogenic endotoxin testing kit (Associates of Cape Cod, lnc.).

Example 20 — Enhanced L-kynurenine degradation in an engineered human ninase variant The h—KYNU enzyme is highly selective towards the hydrolysis of 3’— OH kynurenine and has about 1,000 fold lower tic activity towards L-kynurenine.

Because of its poor catalytic activity towards L-kynurenine, the wild-type human enzyme is not le for therapeutic purposes. To engineer improved L-kynurenine degrading activity into h-KYNU, a saturation mutagenesis library was ucted by overlap extension rase chain reaction (PCR) using the h-KYNU gene and a pair of oligonucleotides designed to introduce mutations of the codon corresponding to amino acid F306. F306 is located within the active site of h-KYNU where it appears to play a role in substrate binding.

The F306 saturation library was screened for activity using the microtiter plate kynureninase assay of Example 6. More than a dozen clones displayed significantly higher activity than wild—type h—KYNU and were selected for further analysis. Sequencing of these clones revealed that two amino acid substitutions at position F306 resulted in increased L— kynurenine ing activity, namely h—KYNU—F306M (SEQ ID NO: 55) and h—KYNU— F306L (SEQ ID NO: 56). These variants were then purified to homogeneity and a detailed kinetic analysis revealed a 2-fold and 5—fold increase in kcat/KM for L-kynurenine for h- KYNU-F306M and h-KYNU-F306L, respectively, as compared to wild-type h-KYNU.

Example 21 — Comparison of Pf-KYNU, anti-PDl, and anti-CTLA-4 therapies in the autologous B16 mouse melanoma model ] The PEGylated Pseudomonas fluorescence kynureninase (PEG—Pf- KYNU) was evaluated in the B16 ma mouse model in a side-by-side comparison with the anti-PDl (clone 4, BioXCell # ) or anti-CTLA-4 (clone UC10-4F10-1 l, ll # BE0032) immune checkpoint inhibitor antibodies. Fifty thousand B16 cells were implanted in the flank of C57BL/6J mice (Day 0, n = 8 mice each group). Once palpable tumors developed (Day 10), the animals were treated with either 250 pg anti-PDl, 100 pg anti-CTLA—4 (200 pg lSt dose as per Holmgaard et a1. (2013)), or 500 pg of PEG—Pf—KYNU at the times shown (. Heat—inactivated PEG-Pf—KYNU was used as a control.

Administration of PEG-Pf-KYNU resulted in significant tumor growth retardation and extended survival in a manner indistinguishable from that ed with the Dl or anti— CTLA-4 checkpoint inhibitor antibodies ( for PEG-Pf-KYNU vs. inactivated enzyme or PBS only.

Example 22 — Efficacy of Mu-KYNU or Pf-KYNU and Dl combination therapy in the autologous B16 mouse melanoma model The PEGylated enzymes (PEG-Pf-KYNU and PEG—Mu-KYNU) were evaluated in B16 melanoma allografts in ation with the anti—PDl immune checkpoint tor antibody (Curran et al., 2010). Four groups of C57BL/6J mice (10 per group) were implanted with 50,000 B16 cells (Day 0) and tumors were allowed to develop. Once palpable tumors ped (Day 10), the animals were treated with 250 pg anti—PDl by IP injection (clone RMPl-l4, BioXCell # BE0146) on days 10, 13, and 16 either with or without 500 pg PEG—Pf—KYNU or 500 pg PEG—Mu-KYNU s.c. near the tumor site. Mice received a total of six doses of KYNU between days 10 and 25. One group was given PBS injections i.p. as a control for PD-l. Tumor growth was drastically ed or even reversed in all treatment arms compared to PBS control (). Importantly, additive s were observed with anti—PDl in combination with KYNU resulting in complete remission of 60% of the tumors with PEG-Pf-KYNU/anti-PDl treatment and 20% of the tumors with PEG-Mu- KYNU/anti-PDl treatment (). Corresponding Kaplan-Meier plots are ed in .

Example 23 — Efficacy of PEG-Mu-KYNU therapies in the autologous B16 mouse melanoma model The PEGylated Mucilagz‘nibacter paludis kynureninase (PEG—Mu— KYNU) was evaluated in the B16 melanoma mouse model. Allografts were initiated by implanting 50,000 B16 cells in the flanks of C57BL/6J mice (Day 0, n = 9 mice per group).

Once palpable tumors developed (Day 10), the animals were d with 500 ug of PEG—Mu- KYNU by aneous ion near the tumor site every three days for a total of 6 doses.

An identical treatment regimen with heat—inactivated PEG—Mu-KYNU was used as a control.

Administration of -KYNU resulted in tumor growth retardation (A) with an extended median survival time of 25 days compared to 22 days for the heat-inactivated PEG- Mu—KYNU control (B).

] All of the methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions and methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be d to the s and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the invention. More specifically, it will be apparent that certain agents which are both chemically and physiologically related may be substituted for the agents described herein while the same or similar results would be achieved. All such similar substitutes and modifications nt to those skilled in the art are deemed to be within the , scope and concept of the invention as defined by the appended claims.

REFERENCES The following nces, to the extent that they provide exemplary procedural or other details supplementary to those set forth herein, are specifically incorporated herein by reference.

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Claims (12)

WHAT IS CLAIMED IS:

1. Use of a kynureninase or a nucleic acid encoding a kynureninase in the manufacture of a medicament for the treatment of a tumor in a subject. 5

2. The use according to claim 1, wherein the kynureninase comprises a mammalian or bacterial kynureninase.

3. The use according to claim 1 or 2, n the kynureninase ses an amino acid sequence at least 90% identical to any of SEQ ID NOs: 7-52 and 57.

4. The use according to any one of claims 1 to 3, wherein the kynureninase comprises an 10 amino acid sequence at least 90% identical to SEQ ID NO: 8 and having at least one substitution relative to native human kynureninase (SEQ ID NO: 8), said at least one substitution including a substitution for a Phe normally found at position 306 of native human kynureninase.

5. The use according to claim 3 or 4, wherein the ninase comprises an amino acid 15 sequence at least 90% identical to SEQ ID NO: 8 with a Met or Phe306Leu substitution at on 306.

6. The use according to any one of claims 1 to 5, wherein the kynureninase is coupled to polyethylene glycol.

7. The use according to any one of claims 1 to 6, wherein the kynureninase further 20 comprises a heterologous peptide segment.

8. The use according to claim 7, wherein the heterologous peptide t is an XTEN peptide, an IgG Fc, an albumin, or an albumin binding peptide.

9. The use according to any one of claims 1 to 8, wherein the kynureninase has greater catalytic activity s kynenurine than 3’-OH kynenurine. 25

10. The use according to any one of claims 1 to 9, wherein the kynureninase has a kcat/KM for nine of at least 0.5 M-1s-1.

11. The use according to claim 1, wherein the tumor is a solid tumor.

12. The use according to claim 1, n the tumor is a hematological tumor.