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US20090257994A1 - Chimeric immunoreceptor useful in treating human cancers - Google Patents

Chimeric immunoreceptor useful in treating human cancers Download PDF

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US20090257994A1
US20090257994A1 US12/314,195 US31419508A US2009257994A1 US 20090257994 A1 US20090257994 A1 US 20090257994A1 US 31419508 A US31419508 A US 31419508A US 2009257994 A1 US2009257994 A1 US 2009257994A1
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cells
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human
glioma
receptor
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Michael Jensen
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City of Hope
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City of Hope
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Priority claimed from US10/134,645 external-priority patent/US20030171546A1/en
Priority claimed from US11/274,344 external-priority patent/US7514537B2/en
Priority to US12/314,195 priority Critical patent/US20090257994A1/en
Application filed by City of Hope filed Critical City of Hope
Publication of US20090257994A1 publication Critical patent/US20090257994A1/en
Priority to PCT/US2009/066714 priority patent/WO2010065818A1/fr
Assigned to CITY OF HOPE reassignment CITY OF HOPE ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: JENSEN, MICHAEL
Priority to US13/046,518 priority patent/US8324353B2/en
Priority to US13/570,032 priority patent/US8497118B2/en
Priority to US13/953,622 priority patent/US9217025B2/en
Priority to US14/976,689 priority patent/US20170209543A9/en
Priority to US16/723,782 priority patent/US11278594B2/en
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Definitions

  • the invention relates to the field of biomedicine and specifically methods useful for cancer therapy.
  • embodiments of the invention relate to methods for specific CTL immunotherapeutic strategies for cancer including the use of genetically-modified T lymphocytes expressing chimeric immunoreceptors in the treatment of human brain tumors and other cancers.
  • Gliomas are the most common type of primary brain tumors; 20,000 cases are diagnosed and 14,000 glioma-related deaths occur annually in the United States 5-8 . Gliomas are heterogeneous with respect to their malignant behavior and, in their most common and aggressive forms, anaplastic astrocytoma (AA-grade III) and glioblastoma multiforme (GBM-grade IV), are rapidly progressive and nearly uniformly lethal 9; 10 .
  • the cornerstones of oncologic management of malignant glioma are resection and radiation therapy 11-16 .
  • the mean duration of survival has increased to 82 weeks for glioblastoma multiforme and 275 weeks for anaplastic astrocytoma, although 5-year survival rates have only increased from 3 to 6% for glioblastoma multiforme and 12.1% for anaplastic astrocytoma 6-8 .
  • the major prognostic indicators for prolonged survival are younger age ( ⁇ 40 yrs) and performance status (KPS score >70) 17 . Resections of >90% of bulky tumors are usually attempted provided that vital functional anatomy is spared.
  • recurrent tumors arise from radiographically enhancing remnants of the original incompletely resected tumor 10; 30; 31 .
  • Provided recurrences are unifocal and amenable in their location to aggressive re-resection, this approach can extend survival duration, particularly for patients with anaplastic astrocytoma and those glioblastoma multiforme patients with a KPS>70.
  • the median survival of recurrent glioblastoma multiforme patients treated with re-resection is 36 weeks 10; 30; 31 .
  • Radiation therapy in the form of either brachytherapy or stereotactic radiosurgery may extend the duration of survival in re-resected recurrent glioblastoma multiforme patients by only 10-12 weeks 32 .
  • the use of chemotherapy in the setting of recurrent disease should be in the context of available clinical trials, as its efficacy in this patient population is unsubstantiated.
  • TK-suicide gene therapy
  • antisense inhibition of tumor growth factor receptors conditionally lethal viral vectors
  • immunotherapy antibody, tumor cell vaccines, immunotoxins, adoptive transfer of activated lymphocytes
  • anti-angiogenesis approaches 33-40 The multiplicity of challenges faced in the development of effective adjuvant therapies for malignant glioma include the extensive infiltrative growth of tumor cells into normal brain parenchyma, the capacity of soluble factors elaborated from these tumors to attenuate the development of immune responses, and the difficulty of establishing clinically meaningful therapeutic ratios when administering therapeutics into the central nervous system (CNS). Early clinical evaluation of novel therapeutics is clearly indicated in this patient population.
  • receptors for transferrin and growth factors have been the subject of experimental glioma therapeutics utilizing ligands for these receptors conjugated to toxins or radionucleotides as a delivery system 41 .
  • the specificity of this approach relies on the unique expression or over-expression of targeted receptors on glioma cells compared to normal brain.
  • some receptor complexes for interleukins utilized by the immune system are expressed by gliomas, in particular high-affinity IL-13 receptors 42-48 .
  • IL-13 receptor trimolecular complex utilized by the immune system, which consists of the IL-13R ⁇ 1, the IL-4R ⁇ , and ⁇ c
  • glioma cells overexpress a unique IL-13R ⁇ 2 chain capable of binding IL-13 independently of the requirement for IL-4R ⁇ or ⁇ c 44; 49; 50 .
  • IL-13 has pleotrophic immunoregulatory activity outside the CNS 51-53 . Both cytokines stimulate IgE production by B lymphocytes and suppress pro-inflammatory cytokine production by macrophages. The immunobiology of IL-13 within the CNS is largely unknown.
  • IL-13R ⁇ 2 stands as the most specific and ubiquitously expressed cell-surface target for glioma described to date.
  • IL-13 cytokine As a strategy to exploit the glioma-specific expression of IL-13R ⁇ 2 in the CNS, molecular constructs of the IL-13 cytokine have been described that fuse various cytotoxins ( Pseudomonas exotoxin and Diptheria toxin) to its carboxyl terminal 55-58 . Internalization of these toxins upon binding to IL-13 receptors is the basis of the selective toxicity of these fusion proteins. These toxins display potent cytotoxicity towards glioma cells in vitro at picomolar concentrations 55 . Human intracranial glioma xenografts in immunodeficient mice can be eliminated by intratumor injection of the IL-13-toxin fusion protein without observed toxicities 55 . These studies support the initiation of clinical investigation utilizing IL-13-directed immunotoxins loco-regionally for malignant glioma.
  • IL-13-based cytotoxins to the broadly expressed IL-13R ⁇ 1/IL-4 ⁇ / ⁇ c receptor complex has the potential of mediating untoward toxicities to normal tissues outside the CNS, and thus limits the systemic administration of these agents.
  • IL-13 has been extensively dissected at the molecular level: structural domains of this cytokine that are important for associating with individual receptor subunits have been mapped 55; 58 Consequently, selected amino acid substitutions in IL-13 have predictable effects on the association of this cytokine with its receptor subunits.
  • IL-13's alpha helix A in particular at amino acid 13, disrupt its ability to associate with IL-4 ⁇ , thereby selectively reducing the affinity of IL-13 to the IL-13R ⁇ 1/IL-4 ⁇ / ⁇ c receptor by a factor of five 55; 57; 58
  • binding of mutant IL-13(E13Y) to IL-13R ⁇ 2 was not only preserved but increased relative to wild-type IL-13 by 50-fold.
  • minimally altered IL-13 analogs can simultaneously increase IL-13's specificity and affinity for glioma cells via selective binding to IL-13R ⁇ 2 relative to normal tissues bearing IL-13R ⁇ 1/IL-4 ⁇ / ⁇ c receptors.
  • Malignant gliomas represent a clinical entity that is highly attractive for immunotherapeutic intervention since 1) most patients with resection and radiation therapy achieve a state of minimal disease burden and 2) the anatomic location of these tumors within the confines of the CNS make direct loco-regional administration of effector cells possible. At least two pathologic studies have demonstrated that the extent of perivascular lymphocytic infiltration in malignant gliomas correlates with an improved prognosis 59-61 . Animal model systems have established that glioma-specific T cells, but not lymphokine-activated killer (LAK) cells, can mediate the regression of intracerebrally implanted gliomas 62-71 .
  • LAK lymphokine-activated killer
  • T cells unlike LAK cells, have the capacity to infiltrate into brain parenchyma and thus can target infiltrating tumor cells that may be distant from the primary tumor.
  • TGF- ⁇ 2 immunosuppressive cytokines
  • prostaglandins which, inhibit the induction/amplification of glioma-reactive T cell responses 72-74 .
  • T cells are activated in situ in the resection cavity.
  • T cells might have significantly increased anti-glioma activity if they are specific for target antigens expressed by gliomas.
  • Chimeric antigen receptors engineered to consist of an extracellular single chain antibody (scFvFc) fused to the intracellular signaling domain of the T cell antigen receptor complex zeta chain (scFvFc: ⁇ ) have the ability, when expressed in T cells, to redirect antigen recognition based on the monoclonal antibody's specificity 98 .
  • the design of scFvFc: ⁇ receptors with target specificities for tumor cell-surface epitopes is a conceptually attractive strategy to generate antitumor immune effector cells for adoptive therapy as it does not rely on pre-existing anti-tumor immunity.
  • receptors are “universal” in that they bind antigen in a MHC independent fashion, thus, one receptor construct can be used to treat a population of patients with antigen-positive tumors.
  • Several constructs for targeting human tumors have been described in the literature including receptors with specificities for Her2/Neu, CEA, ERRB-2, CD44v6, and epitopes selectively expressed on renal cell carcinoma 98-104 . These epitopes all share the common characteristic of being cell-surface moieties accessible to scFv binding by the chimeric T cell receptor. In vitro studies have demonstrated that both CD4+ and CD8+ T cell effector functions can be triggered via these receptors.
  • scFvFc: ⁇ expressing T cells to eradicate established tumors 105 .
  • the function of primary human T cells expressing tumor-specific scFvFc: ⁇ receptors have been evaluated in vitro; these cells specifically lyse tumor targets and secrete an array of pro-inflammatory cytokines including IL-2, TNF, IFN- ⁇ , and GM-CSF 104 .
  • CD20-specific scFvFc: ⁇ receptor construct for the purpose of targeting CD20+B-cell malignancy and an L1-CAM-specific chimeric immunoreceptor for targeting neuroblastoma 106 .
  • Preclinical laboratory studies have demonstrated the feasibility of isolating and expanding from healthy individuals and lymphoma patients CD8+ CTL clones that contain a single copy of unrearranged chromosomally integrated vector DNA and express the CD20-specific scFvFc: ⁇ receptor 107 .
  • purified linear plasmid DNA containing the chimeric receptor sequence under the transcriptional control of the CMV immediate/early promoter and the NeoR gene under the transcriptional control of the SV40 early promoter was introduced into activated human peripheral blood mononuclear cells by exposure of cells and DNA to a brief electrical current, a procedure called electroporation.
  • electroporation Utilizing selection, cloning, and expansion methods currently employed in FDA-approved clinical trials at the Fred Hutchinson Cancer Research Center, Seattle, Wash., gene modified CD8+ CTL clones with CD20-specific cytolytic activity have been generated from each of six healthy volunteers in 15 separate electroporation procedures. These clones when co-cultured with a panel of human CD20+ lymphoma cell lines proliferate, specifically lyse target cells, and are stimulated to produce cytokines.
  • the present invention relates to chimeric transmembrane immunoreceptors, named “zetakines,” comprised of an extracellular domain comprising a soluble receptor ligand linked to a support region capable of tethering the extracellular domain to a cell surface, a transmembrane region and an intracellular signaling domain. Zetakines, when expressed on the surface of T lymphocytes, direct T cell activity to those cells expressing a receptor for which the soluble receptor ligand is specific.
  • Zetakine chimeric immunoreceptors represent a novel extension of antibody-based immunoreceptors for redirecting the antigen specificity of T cells, with application to treatment of a variety of cancers, particularly via the autocrine/paracrine cytokine systems utilized by human malignancy.
  • a mutant of the IL-13 cytokine, IL-13(E13Y), having selective high-affinity binding to IL-13R ⁇ 2 has been converted into a type I transmembrane chimeric immunoreceptor capable of redirecting T cell antigen specificity to IL-13R ⁇ 2-expressing tumor cells.
  • This embodiment of the zetakine consists of extracellular IL-13(E13Y) fused to human IgG4 Fc, transmembrane CD4, and intracellular T cell antigen receptor CD3 complex zeta chain.
  • Analogous immunoreceptors can be created that are specific to any of a variety of cancer cell types that selectively express receptors on their cell surfaces, for which selective ligands are known or can be engineered.
  • T cells Bulk lines and clones of human T cells stably transformed to express such an immunoreceptor display redirected cytolysis of the cancer cell type to which they are specific, while showing negligible toxicity towards non-target cells.
  • Such engineered T cells are a potent and selective therapy for malignancies, including difficult to treat cancers such as glioma.
  • FIG. 1 Results of a Western Blot showing that the IL13zetakine Chimeric Immunoreceptor is expressed as an intact glycosylated protein in Jurkat T cells.
  • FIG. 2 Results of flow cytometric analysis showing that expressed IL13zetakine chimeric immunoreceptor trafficks to the cell-surface as a type I transmembrane protein.
  • FIG. 3 Results of flow cytometric analysis showing the cell surface phenotype of a representative primary human IL13zetakine + CTL clone.
  • FIG. 4 Results of chromium release assays.
  • FIG. 4A shows that the IL13zetakine + CTL clone acquired glioma-specific re-directed cytolytic activity
  • FIG. 4B shows the profile of anti-glioma cytolytic activity by primary human IL13zetakine + CD8 + CTL clones was observed in glioma cells generally.
  • FIG. 5 Results of in vitro stimulation of cytokine production, showing that IL13zetakine + CTL clones are activated for cytokine production by glioma stimulator cells.
  • FIG. 6 Results of in vitro stimulation of cytokine production ( FIG. 6A , IFN ⁇ ; FIG. 6B , TNF ⁇ ; FIG. 6C , GM-CSF), showing the specific inhibition of IL13zetakine + CTL activation for cytokine production by anti-IL13R Mab and rhIL13.
  • FIG. 7 Results of growth studies.
  • FIG. 7A shows that IL13zetakine + CD8 + CTL cells proliferate upon co-culture with glioma stimulators
  • FIG. 7B shows the inhibition of glioma-stimulated proliferation of IL13zetakine + CD8 + CTL cells by rhIL-13.
  • FIG. 8 Flow chart of the construction of IL13zetakine/HyTK-pMG ( FIG. 8A , construction fo hsp-IL13-IgG4 (SmP)-hinge-Fe-Zeta; FIG. 8B , construction of IL13-Fc; ⁇ 3pMB ⁇ Pac; FIG. 8C , construction of Il13/HyTK-pMG).
  • FIG. 9 Plasmid map of IL13zetakine/HyTK-pMG.
  • FIG. 10 Plasmid map of alternative IL13zetakine/HyTK-pMG.
  • FIG. 11 Schematic diagram showing structure of IL13 zetakine insert.
  • FIG. 12 Nucleic acid sequence of a plasmid DNA vector (upper strand: SEQ ID NO:14; lower strand:SEQ ID NO:16) and the corresponding amino acid sequence of IL13zetakine (SEQ ID NO:17) and HyTK (SEQ ID NO:18).
  • FIG. 13 Nucleic acid sequence of an alternate plasmid DNA vector (upper strand: SEQ ID NO:19; lower strand:SEQ ID NO:20) and the corresponding amino acid sequence of IL13zetakine (SEQ ID NO:21) and HyTK (SEQ ID NO:22).
  • FIG. 14 Nucleic acid sequence of an alternate plasmid DNA vector (SEQ ID NO:23).
  • An ideal cell-surface epitope for tumor targeting with genetically-engineered re-directed T cells would be expressed solely on tumor cells in a homogeneous fashion and on all tumors within a population of patients with the same diagnosis. Modulation and/or shedding of the target molecule from the tumor cell membrane may also impact on the utility of a particular target epitope for re-directed T cell recognition. To date few “ideal” tumor-specific epitopes have been defined and secondary epitopes have been targeted based on either lack of expression on critical normal tissues or relative over-expression on tumors.
  • the intracavitary administration of T cells for the treatment of this cancer permits the expansion of target epitopes to those expressed on tumor cells but not normal CNS with less stringency on expression by other tissues outside the CNS.
  • the concern regarding toxicity from cross-reactivity of tissues outside the CNS is mitigated by a) the sequestration of cells in the CNS based on the intracavitary route of administration and b) the low cell numbers administered in comparison to cell doses typically administered systemically.
  • the IL-13R ⁇ 2 receptor stands out as the most ubiquitous and specific cell-surface target for malignant glioma 47 . Sensitive autoradiographic and immunohistochemical studies fail to detect IL-13 receptors in the CNS 46; 48 . Moreover, mutation of the IL-13 cytokine to selectively bind the glioma-restricted IL-13R ⁇ 2 receptor is a further safeguard against untoward reactivity of IL-13-directed therapeutics against IL-13R ⁇ 1/IL-4 ⁇ +normal tissues outside the CNS 55; 57 .
  • IL-13R ⁇ 2 The potential utility of targeting glioma IL-13R ⁇ 2 the design and testing of a novel engineered chimeric immunoreceptor for re-directing the specificity of T cells that consists of an extracellular IL-13 mutant cytokine (E13Y) tethered to the plasma membrane by human IgG4 Fc which, in turn, is fused to CD4TM and the cytoplasmic tail of CD3 zeta.
  • This chimeric immunoreceptor has been given the designation of “IL-13 zetakine.”
  • the IL-13R ⁇ 2 receptor/IL-13(E13Y) receptor-ligand pair is an excellent guide for understanding and assessing the suitability of receptor-ligand pairs generally for use in zetakines.
  • An ideal zetakine comprises an extracellular soluble receptor ligand having the properties of IL-13(E13Y) (specificity for a unique cancer cell surface receptor, in vivo stability due to it being derived from a naturally-occurring soluble cell signal molecule, low immunogenicity for the same reason).
  • soluble receptor ligands as distinct advantages over the prior art use of antibody fragments (such as the scFvFc immunoreceptors) or cell adhesion molecules, in that soluble receptor ligands are more likely to be stable in the extracellular environment, non-antigenic, and more selective.
  • Chimeric immunoreceptors comprise an extracellular domain comprised of a soluble receptor ligand linked to an extracellular support region that tethers the ligand to the cell surface via a transmembrane domain, in turn linked to an intracellular receptor signaling domain.
  • suitable soluble receptor ligands include autocrine and paracrine growth factors, chemokines, cytokines, hormones, and engineered artificial small molecule ligands that exhibit the required specificity.
  • Natural ligand sequences can also be engineered to increase their specificity for a particular target cell.
  • a soluble receptor ligand for use in a particular zetakine is governed by the nature of the target cell, and the qualities discussed above with regard to the IL-13(E13Y) molecule, a preferred ligand for use against glioma.
  • suitable support regions include the constant (Fc) regions of immunoglobins, human CD8 ⁇ , and artificial linkers that serve to move the targeting moiety away from the cell surface for improved access to receptor binding on target cells.
  • a preferred support region is the Fc region of an IgG (such as IgG4).
  • suitable transmembrane domains include the transmembrane domains of the leukocyte CD markers, preferably that of CD8.
  • intracellular receptor signaling domains are those of the T cell antigen receptor complex, preferably the zeta chain of CD3 also Fc ⁇ RIII costimulatory signaling domains, CD28, DAP10, CD2, alone or in a series with CD3zeta.
  • the human IL-13 cDNA having the E13Y amino acid substitution was synthesized by PCR splice overlap extension.
  • a full length IL-13 zetakine construct was assembled by PCR splice overlap extension and consists of the human GM-CSF receptor alpha chain leader peptide, IL-13(E13Y)-Gly-Gly-Gly, human IgG4 Fc, human CD4TM, and human cytoplasmic zeta chain.
  • This cDNA construct was ligated into the multiple cloning site of a modified pMG plasmid under the transcriptional control of the human Elongation Factor-1alpha promoter (Invivogen, San Diego).
  • This expression vector co-expresses the HyTK cDNA encoding the fusion protein HyTK that combines in a single molecule hygromycin phosphotransferase activity for in vitro selection of transfectants and HSV thymidine kinase activity for in vivo ablation of cells with ganciclovir from the CMV immediate/early promoter.
  • Western blot of whole cell Jurkat lysates pre-incubated with tunicamycin, an inhibitor of glycosylation, with an anti-zeta antibody probe demonstrated that the expected intact 56-kDa chimeric receptor protein is expressed. This receptor is heavily glycosylated consistent with post-translational modification of the native IL-13 cytokine 108 .
  • Flow cytometric analysis of IL-13 zetakine+ Jurkat cells with anti-human IL-13 and anti-human Fc specific antibodies confirmed the cell-surface expression of the IL-13 zetakine as a type I transmembrane protein.
  • IL-13 zetakine+ CD8+ CTL clones display robust proliferative activity in ex vivo expansion cultures.
  • Expanded clones display re-directed cytolytic activity in 4-hr chromium release assays against human IL-13R ⁇ 2+ glioblastoma cell lines. The level of cytolytic activity correlates with levels of zetakine expression on T cells and IL-13R ⁇ 2 receptor density on glioma target cells.
  • IL-13 zetakine+ clones are activated for cytokine secretion (IFN- ⁇ , TNF- ⁇ , GM-CSF).
  • Activation was specifically mediated by the interaction of the IL-13 zetakine with the IL-13R ⁇ 2 receptor on glioma cells since CTL clones expressing an irrelevant chimeric immunoreceptor do not respond to glioma cells, and, since activation can be inhibited in a dose-dependent manner by the addition to culture of soluble IL-13 or blocking antibodies against IL-13 on T cell transfectants and IL-13R ⁇ 2 on glioma target cells.
  • IL-13 zetakine-expressing CD8+ CTL clones proliferate when stimulated by glioma cells in culture.
  • IL-13 zetakine+ CTL clones having potent anti-glioma effector activity will have significant clinical activity against malignant gliomas with limited collateral damage to normal CNS.
  • An immunoreceptor according to the present invention can be produced by any means known in the art, though preferably it is produced using recombinant DNA techniques.
  • a nucleic acid sequence encoding the several regions of the chimeric receptor can prepared and assembled into a complete coding sequence by standard techniques of molecular cloning (genomic library screening, PCR, primer-assisted ligation, site-directed mutagenesis, etc.).
  • the resulting coding region is preferably inserted into an expression vector and used to transform a suitable expression host cell line, preferably a T lymphocyte cell line, and most preferably an autologous T lymphocyte cell line.
  • a third party derived T cell line/clone a transformed humor or xerogenic immunologic effector cell line, for expression of the immunoreceptor.
  • NK cells, macrophages, neutrophils, LAK cells, LIK cells, and stem cells that differentiate into these cells can also be used.
  • lymphocytes are obtained from a patient by leukopharesis, and the autologous T cells are transduced to express the zetakine and administered back to the patient by any clinically acceptable means, to achieve anti-cancer therapy.
  • Suitable doses for a therapeutic effect would be between about 10 6 and about 10 9 cells per dose, preferably in a series of dosing cycles.
  • a preferred dosing regimen consists of four one-week dosing cycles of escalating doses, starting at about 10 7 cells on Day 0, increasing incrementally up to a target dose of about 10 8 cells by Day 5.
  • Suitable modes of administration include intravenous, subcutaneous, intracavitary (for example by reservoir-access device), intraperitoneal, and direct injection into a tumor mass.
  • the coding sequence for an immunoreceptor according to the present invention was constructed by de novo synthesis of the IL13(E13Y) coding sequence using the following primers (see FIG. 8 for a flow chart showing the construction of the immunoreceptor coding sequence and expression vector):
  • IL13P1 EcoRI (SEQ ID NO. 1) TAT GAATTC ATGGCGCTTTTGTTGACCACGGTCATTGCTCTCACTTGCCT TGGCGGCTTTGCCTCCCCAGGCCCTGTGCCTCCCTCTACAGCCCTCAGGT AC IL13P2: (SEQ ID NO. 2) GTTGATGCTCCATACCATGCTGCCATTGCAGAGCGGAGCCTTCTGGTTCT GGGTGATGTTGACCAGCTCCTCAATGAGGTACCTGAGGGCTGTAGAGGG AG IL13P3: (SEQ ID NO.
  • CTCTGGGTCTTCTCGATGGCACTGCAGCCTGACACGTTGATCAGGGATTC CAGGGCTGCACAGTACATGCCAGCTGTCAGGTTGATGCTCCATACCATGC IL13P4: (SEQ ID NO. 4) CCTCGATTTTGGTGTCTCGGACATGCAAGCTGGAAAACTGCCCAGCTGAG ACCTTGTGCGGGCAGAATCCGCTCAGCATCCTCTGGGTCTTCTCGATGGC IL13P5: BamHI (SEQ ID NO. 5) TC GGATCC TCAGTTGAACCGTCCCTCGCGAAAAAGTTTCTTTAAATGTAA GAGCAGGTCCTTTACAAACTGGGCCACCTCGATTTTGGTGTCTCGG
  • Ligation 312#3 was mutagenized (stratagene kit, per manufacturer's instructions) to fix a deleted nucleotide using the primers 5′: IL13 312#3 mut5-3 (CAACCTGACAGCTGGCATGTACTGTGCAGCCCTGGAATC (SEQ ID NO. 6)) and 3′:IL13 312#3 mut3-5 (GATTCCAGGGCTGCACAGTACATGCCAGCTGTCAGGTTG (SEQ ID NO. 7)), and ligation 312#3 as a template, to form ligation 348#1 (IL13zetakine/pSK).
  • the coding Human GM-CSFR alpha chain Signal Peptide (hsp) coding sequence was fused to the 5′ end of IL13(E13Y) by standard PCR splice overlap extension.
  • the hsp sequence (101 bp) was obtained from the template ligation 301 #10 (hsp/pSK) (human GCSF receptor ⁇ -chain leader sequence from human T cell cDNA), using the primers 5′:19hsp5′ (ATCTCTAGAGCCGCCACCATGCTTCTCCTGGTGACAAGCCTTC (SEQ ID NO.
  • hsp-IL13FR (GAGGGAGGCACAGGGCCTGGGATCAGGAGGAATG (SEQ ID NO. 9)
  • the IL-13 sequence (371 bp) was obtained using the primers 5′: hsp-IL13FF (CATTCCTCCTGATCCCAGGCCCTGTGCCTCCCTC (SEQ ID NO. 10)) and 3′: IL13-IgG4FR (GGGACCATATTTGGACTCGTTGAACCGTCCCTCGC (SEQ ID NO. 11)), and ligation 312#3 as template.
  • Fusion was achieved using the 101 bp hsp sequence and 371 bp IL13 sequence thus obtained, and the primers 5′: 19hsp5′ and 3′: IL13-IgG4FR, to yield a 438 bp fusion hsp-IL13 sequence.
  • IgG4 Fc region IgG4m:zeta was fused to the 3′ end of the hsp-IL13 fusion sequence using the same methods.
  • the IgG4m:zeta sequence (1119 bp) was obtained using the primers 5′: IL13-IgG4FF (GCGAGGGACGGTTCAACGAGTCCAAATATGGTCCC (SEQ ID NO. 12)) and 3′: ZetaN3′ (ATGCGGCCGCTCAGCGAGGGGGCAGG (SEQ ID NO. 13)) (NotI site highlighted in bold), using the sequence R9.10 (IgG4mZeta/pSK) as template.
  • the 1119 bp IgG4m:zeta sequence was fused to the hsp-IL13 fusion sequence using the respective sequences as templates, and the primers 5′: 19hsp5′ and 3′: ZetaN3′, to yield a 1522 bp hsp-IL13-IgG4m:zeta fusion sequence.
  • the ends were digested with XbaI-NotI, and ligated into pSK as ligation 351#7, to create the plasmid IL13zetakine/pSK (4464 bp).
  • An expression vector containing the IL13 zetakine coding sequence was created by digesting the IL13zetakine/pSK of Example 1 with XbaI-NotI, and creating blunt ends with Klenow, and ligating the resulting fragment into the plasmid pM ⁇ Pac (Invirogen) (first prepared by opening with SgrAI, blunting with Klenow, and dephosphorylation with SAP), to yield the plasmid IL13zetakine/pMG. See FIG. 8 .
  • IL13zetakine/pMG The hygromycin resistance region of IL13zetakine/pMG was removed by digestion with NotI-NheI, and replaced by the selection/suicide fusion HyTK, obtained from plasmid CE7RIHyTK-pMG (Jensen, City of Hope) by digestion with NotI-NheI, to create the expression vector IL13zetakine/HyTK-pMG (6785 bp).
  • This plasmid comprises the Human Elongation Factor-1 ⁇ promoter (hEF1p) at bases 6-549, the IL13zetakine coding sequence at bases 692-2185, the Simian Virus 40 Late polyadenylation signal (Late SV40pAN) at bases 2232-2500, a minimal E.
  • coli origin of replication (Ori ColE1) at bases 2501-3247, a synthetic poly A and Pause site (SpAN) at bases 3248-3434, the Immeate-early CMV enhancer/promoter (h CMV-1Aprom) at bases 3455-4077, the Hygromycin resistance-Thymidine kinase coding region fusion (HyTK) at bases 4259-6334, and the bovine growth hormone polyadenylation signal and a transcription pause (BGh pAn) at bases 6335-6633.
  • the plasmid has a PacI linearization site at bases 3235-3242.
  • IL13zetakine/HyTK-pMG is a modified pMG backbone, expressing the IL13zetakine gene from the hEF1 promoter, and the HyTK fusion from the h CMV-1A promoter.
  • FIG. 9 A map of the plasmid IL13zetakine/HyTK-pMG appears in FIG. 9 .
  • the full nucleic acid sequence of the plasmid is shown in FIG. 12 .
  • the sequence of an IL13zetakine insert is given as SEQ ID NO:15, below. See also FIG. 11 .
  • FIG. 1 Jurkat T cell stable transfectants (Jurkat-IL13-pMG bulk line) were obtained by electroporating Jurkat T cells with the IL13zetakine/HyTK-pMG expression vector, followed by selection and expansion of positive transfectants.
  • 2 ⁇ 10 6 cells from the Jurkat-IL13-pMG bulk line were plated per well in a 24-well plate with or without 5 ⁇ g/ml, 10 ⁇ g/ml, or 20 ⁇ g/ml Tunicamycin. The plate was incubated at 37° C. for 22 hrs. Cells were harvested from each well, and each sample was washed with PBS and resuspended in 50 ⁇ l RIPA buffer (PBS, 1% NP40, 0.5% sodium deoxycholate, 0.1% SDS) containing 1 tablet/10ml Complete Protease Inhibitor Cocktail (Boehringer Mannheim, Indianapolis, Ind.).
  • RIPA buffer PBS, 1% NP40, 0.5% sodium deoxycholate, 0.1% SDS
  • Samples were incubated on ice for 30 minutes then disrupted by aspiration with syringe with 21 gauge needle then incubated on ice for an additional 30 minutes before being centrifuged at 4° C. for 20 minutes at 14,000 rpm. Samples of centrifuged lysate supernatant were harvested and boiled in an equal volume of sample buffer under reducing conditions, then subjected to SDS-PAGE electrophoresis on a 12% acrylamide gel. Following transfer to nitrocellulose, membrane was allowed to dry O/N at 4° C.
  • membrane was blocked in a Blotto solution containing 0.04 gm/ml non-fat dried milk in T-TBS (0.02% Tween 20 in Tris buffered saline pH 8.0) for 1 hour.
  • Membrane was then incubated with primary mouse anti-human CD3 ⁇ monoclonal antibody (Pharmingen, San Diego, Calif.) at a concentration of 1 ⁇ g/ml for 2 hours, washed, and then incubated with a 1:3000 dilution (in Blotto solution) of goat anti-mouse IgG alkaline phosphatase conjugated secondary antibody (Bio-Rad ImmunoStar Kit, Hercules, Calif.) for 1 hour.
  • membrane Prior to developing, membrane was washed 4 additional times in T-TBS, and then incubated with 3 ml of phosphatase substrate solution (Biorad ImmunoStar Kit, Hercules, Calif.) for 5 minutes at room temperature. Membrane was then covered with plastic, and exposed to x-ray film. Consistant with the known glycosylation pattern of wild-type human IL-13, the electrophoretic mobility of expressed IL-13(E13Y) zetakine is demonstrative of a heavily glycosylated protein which, when expressed in the presence of tunicamycin, is reduced to an amino acid backbone of approximately 54 kDa.
  • PE phycoerythrin
  • FITC fluorescein isothiocyanate
  • Jurkat IL13zetakine-pMG transfectants were stained with anti-human Fc(FITC) antibody (Jackson ImmunoResearch, West Grove, Pa.), recombinant human IL13R ⁇ 2/human IgG1 chimera (R&D Systems, Minneapolis, Minn.) followed by FITC-conjugated anti human-IgG1 monoclonal antibody (Sigma, St. Louis, Mo.), and an anti-IL13(PE) antibody (Becton Dickinson, San Jose, Calif.) for analysis of cell surface chimeric receptor expression.
  • FITC Fluorescence ImmunoResearch
  • R&D Systems recombinant human IL13R ⁇ 2/human IgG1 chimera
  • FITC-conjugated anti human-IgG1 monoclonal antibody Sigma, St. Louis, Mo.
  • an anti-IL13(PE) antibody Becton Dickinson, San Jose, Calif.
  • Healthy donor primary cells were also stained with FITC-conjugated anti-CD4, anti-CD8, anti-TCR, and isotype control monoclonal antibodies (Becton Dickinson, San Jose, Calif.) to assess cell surface phenotype.
  • 10 6 cells were washed and resuspended in 100 ⁇ l of PBS containing 2% FCS, 0.2 mg/ml NaN 3 , and 5 ⁇ l of stock antibody. Following a 30 minute incubation at 4° C., cells were washed twice and either stained with a secondary antibody, or resuspended in PBS containing 1% paraformaldehyde and analyzed on a FACSCaliber cytometer.
  • IL-13(E13Y) tethered to the cell membrane by human IgG4 Fc (i.e., IL13(E13Y) zetakine), is capable of binding to its target IL13R ⁇ 2 receptor as assessed by flow cytometric analysis using soluble IL13R ⁇ 2-Fc fusion protein.
  • FIG. 3 Cloned human PBMC IL13zetakine-pMG transfectants were obtained by electroporating PBMC with the IL13zetakine/HyTK-pMG expression vector, followed by selection and expansion of positive transfectants 107 .
  • IL13zetakine + CTL clonal cells were stained with a fluorescein isothiocyanate (FITC)-conjugated mouse anti-human Fc (gamma) fragment-specific F(ab′) 2 (Jackson ImmunoResearch, West Grove, Pa.), recombinant human IL13R ⁇ 2/human IgG1 chimera (R&D Systems, Minneapolis, Minn.) followed by FITC-conjugated anti human-IgG1 monoclonal antibody (Sigma, St.
  • FITC fluorescein isothiocyanate
  • mouse anti-human Fc (gamma) fragment-specific F(ab′) 2 Jackson ImmunoResearch, West Grove, Pa.
  • recombinant human IL13R ⁇ 2/human IgG1 chimera R&D Systems, Minneapolis, Minn.
  • FITC-conjugated anti human-IgG1 monoclonal antibody Sigma, St.
  • IL-13(E13Y) zetakine as a surrogate antigen receptor for primary human T cells was evaluated.
  • Primary human T cells were electroporated with the plasmid expression vector. Positive transformants were selected with hygromycin, cloned in limiting dilution, then expanded by recursive stimulation cycles with OKT3, IL-2 and irradiated feeder cells.
  • Clones demonstrating IL 13zetakine expression by Western blot and FACS were then subjected to functional evaluation in 4-hr chromium release assays against a variety of IL-13 ⁇ 2 + /CD20 ⁇ glioma cell lines (U251, SN-B19, U138), and the IL-13 ⁇ ⁇ /CD20 + B cell lymphocyte line Daudi). These tests showed that IL13zetakine conferred cytolytic activity that was specific for glioma cells ( FIG. 4 a ), and that this specific cytolytic activity is present for glioma cells as a class ( FIG. 4 b ).
  • MJ-IL13-pMG clones The cytolytic activity of MJ-IL13-pMG clones was assayed by employing 51 Cr-labeled SN-B19, U251, and U138 glioma cell lines (IL13 ⁇ 2+/CD20 ⁇ ) and Daudi (CD20+/IL13 ⁇ 2 ⁇ ) as targets.
  • MJ-IL13 effectors were assayed 8-12 days following stimulation. Effectors were harvested, washed, and resuspended in assay media: 2.5 ⁇ 10 5 , 1.25 ⁇ 10 5 , 2.5 ⁇ 10 4 , and 5 ⁇ 10 3 effectors were cultured in triplicate at 37° C. for 4 hours with 5 ⁇ 10 3 target cells in 96-well V-bottom microtiter plates. After incubation, 100 ⁇ l aliquots of cell-free supernatant were harvested and 51 Cr in the supernatants was assayed with a ⁇ -counter. Percent specific cytolysis was calculated as follows:
  • Control wells contained target cells incubated in the presence of target cells alone. Maximum 51 Cr release was determined by measuring the 51 Cr released by labeled target cells in the presence of 2% SDS.
  • Bulk lines of stabley transfected human T cells consisting of approximately 40% IL-13(E13Y) zetakine + TCR ⁇ / ⁇ + lymphocytes displayed re-directed cytolysis specific for 13R ⁇ 2 + glioma targets in 4-hr chromium release assays (>50% specific lysis at E:T ratios of 25:1), with negligable acitivity against IL-13R ⁇ 2-targets ( ⁇ 8% specific lysis at E:T ratios of 25:1).
  • IL-13(E13Y) zetakine + CD8 + TCR ⁇ / ⁇ + CTL clones selected on the basis of high-level binding to anti-IL-13 antibody also display redirected IL13R ⁇ 2-specific glioma cell killing.
  • FIGS. 5-7 MJ-IL13-pMG Cl.
  • F2 responder cells expressing the IL13 zetakine were evaluated for receptor-mediated triggering of IFN ⁇ , GM-CSF, and TNF ⁇ production in vitro.
  • 2 ⁇ 10 6 responder cells were co-cultured in 24-well tissue culture plates with 2 ⁇ 10 5 irradiated stimulator cells (Daudi, Fibroblasts, Neuroblastoma 10HTB, and glioblastoma U251) in 2 ml total.
  • Blocking rat anti-human-IL13 monoclonal antibody (Pharmingen, San Diego, Calif.), recombinant human IL13 (R&D Systems, Minneapolis, Minn.), and IL13R ⁇ 2-specific goat IgG (R&D Systems, Minneapolis, Minn.) were added to aliquots of U251 stimulator cells (2 ⁇ 10 5 /ml) at concentrations of 1 ng/ml, 10 ng/ml, 100 ng/ml, and 1 ⁇ g/ml, 30 minutes prior to the addition of responder cells. Plates were incubated for 72 hours at 37° C., after which time culture supernatants were harvested, aliquoted, and stored at ⁇ 70° C.
  • ELISA assays for IFN ⁇ , GM-CSF, and TNF ⁇ were carried out using the R&D Systems (Minneapolis, Minn.) kit per manufacturer's instructions. Samples were tested in duplicate wells undiluted or diluted at 1:5 or 1:10. The developed ELISA plate was evaluated on a microplate reader and cytokine concentrations determined by extrapolation from a standard curve. Results are reported as picograms/ml, and show strong activation for cytokine production by glioma stimulator cells. FIG. 5 , FIG. 6 .
  • IL-2 independent proliferation of IL13zetakine + CD8 + CTL was observed upon co-cultivation with glioma stimulators ( FIG. 7 a ), but not with IL13 R ⁇ 2 stimulators.
  • Proliferation was inhibited by the addition of rhIL-13 antibody ( FIG. 7 b ), showing that the observed proliferation was dependant on binding of zetakine to the IL-13R ⁇ 2 glioma cell-specific receptor.
  • the mononuclear cells are separated from heparinized whole blood by centrifugation over clinical grade Ficoll (Pharmacia, Uppsula, Sweden).
  • PBMC are washed twice in sterile phosphate buffered saline (Irvine Scientific) and suspended in culture media consisting of RPMI 1640 HEPES, 10% heat inactivated FCS, and 4 mM L-glutamine.
  • T cells present in patient PBMC are polyclonally activated by addition to culture of Orthoclone OKT3 (30 ng/ml). Cell cultures are then incubated in vented T75 tissue culture flasks in the study subject's designated incubator. Twenty-four hours after initiation of culture rhIL-2 is added at 25 U/ml.
  • PBMC Three days after the initiation of culture PBMC are harvested, centrifuged, and resuspended in hypotonic electroporation buffer (Eppendorf) at 20 ⁇ 10 6 cells/ml. 25 ⁇ g of the plasmid IL13zetakine/HyTK-pMG of Example 3, together with 400 ⁇ l of cell suspension, are added to a sterile 0.2 cm electroporation cuvette. Each cuvette is subjected to a single electrical pulse of 250V/40 ⁇ s and again incubated for ten minutes at RT. Surviving cells are harvested from cuvettes, pooled, and resuspended in culture media containing 25 U/ml rhIL-2.
  • hypotonic electroporation buffer Eppendorf
  • Flasks are placed in the patient's designated tissue culture incubator. Three days following electroporation hygromycin is added to cells at a final concentration of 0.2 mg/ml. Electroporated PBMC are cultured for a total of 14 days with media and IL-2 supplementation every 48-hours.
  • hygromycin-resistant CD8+ CTL from electroporated OKT3-activated patient PBMC is initiated on day 14 of culture. Briefly, viable patient PBMC are added to a mixture of 100 ⁇ 10 6 cyropreserved irradiated feeder PBMC and 20 ⁇ 10 6 irradiated TM-LCL in a volume of 200 ml of culture media containing 30 ng/ml OKT3 and 50 U/ml rhIL-2. This mastermix is plated into ten 96-well cloning plates with each well receiving 0.2 ml. Plates are wrapped in aluminum foil to decrease evaporative loss and placed in the patient's designated tissue culture incubator. On day 19 of culture each well receives hygromycin for a final concentration of 0.2 mg/ml. Wells are inspected for cellular outgrowth by visualization on an inverted microscope at Day 30 and positive wells are marked for restimulation.
  • each cloning well with cell growth is individually transferred to T25 flasks containing 50 ⁇ 10 6 irradiated PBMC, 10 ⁇ 10 6 irradiated LCL, and 30 ng/mlOKT3 in 25 mls of tissue culture media.
  • T25 flasks containing 50 ⁇ 10 6 irradiated PBMC, 10 ⁇ 10 6 irradiated LCL, and 30 ng/mlOKT3 in 25 mls of tissue culture media.
  • On day 5 of the stimulation cycle flasks are also supplemented with hygromycin 0.2 mg/ml.
  • CTL selected for expansion for possible use in therapy are analyzed by immunofluorescence on a FACSCalibur housed in CRB-3006 using FITC-conjugated monoclonal antibodies WT/31 (a ⁇ TCR), Leu 2a (CD8), and OKT4 (CD4) to confirm the requisite phenotype of clones ( ⁇ TCR+, CD4 ⁇ , CD8+, and IL13+). Criteria for selection of clones for clinical use include uniform TCR ⁇ +, CD4 ⁇ , CD8+ and IL13+ as compared to isotype control FITC/PE-conjugated antibody. A single site of plasmid vector chromosomal integration is confirmed by Southern blot analysis.
  • DNA from genetically modified T cell clones will be screened with a DNA probe specific for the plasmid vector.
  • Probe DNA specific for the HyTK in the plasmid vector is synthesized by random priming with fluorescein-conjugated dUTP per the manufacture's instructions (Amersham, Arlington Hts, Ill.).
  • T cell genomic DNA is isolated per standard technique. Ten micrograms of genomic DNA from T cell clones is digested overnight at 37° C. then electrophoretically separated on a 0.85% agarose gel. DNA is then transferred to nylon filters (BioRad, Hercules, Calif.) using an alkaline capillary transfer method.
  • Filters are hybridized overnight with probe in 0.5 M Na 2 PO 4 , pH 7.2, 7% SDS, containing 10 ⁇ g/ml salmon sperm DNA (Sigma) at 65° C. Filters are then washed four times in 40 mM Na 2 PO 4 , pH 7.2, 1% SDS at 65° C. and then visualized using a chemiluminescence AP-conjugated anti-florescein antibody (Amersham, Arlington Hts, Ill.). Criteria for clone selection is a single band unique vector band.
  • IL-13 zetakine is determined by Western blot procedure in which chimeric receptor protein is detected with an anti-zeta antibody.
  • Whole cell lysates of transfected T cell clones are generated by lysis of 2 ⁇ 10 7 washed cells in 1 ml of RIPA buffer (PBS, 1% NP40, 0.5% sodium deoxycholate, 0.1% SDS) containing 1 tablet/10 ml Complete Protease Inhibitor Cocktail (Boehringer Mannheim).
  • Membranes are washed in T-TBS (0.05% Tween 20 in Tris buffered saline pH 8.0) then incubated with primary mouse anti-human CD3 ⁇ monoclonal antibody 8D3 (Pharmingen, San Diego, Calif.) at a concentration of 1 ⁇ g/ml for 2 hours. Following an additional four washes in T-TBS, membranes are incubated with a 1:500 dilution of goat anti-mouse IgG alkaline phosphatase-conjugated secondary antibody for 1 hour. Prior to developing, membranes are rinsed in T-TBS then developed with 30 ml of “AKP” solution (Promega, Madison, Wis.) per the manufacturer's instructions. Criteria for clone selection is the presence of a chimeric zeta band.
  • the requirements for target IL-13R ⁇ 2 epitope expression and class I MHC independent recognition will be confirmed by assaying each a ⁇ TCR+, CD8+, CD4 ⁇ , IL-13 zetakine+ CTL clones against IL-13R ⁇ 2+ Daudi cell transfectants and IL-13R ⁇ 2 ⁇ Daudi cells.
  • T cell effectors are assayed 12-14 days following stimulation with OKT3.
  • Effectors are harvested, washed, and resuspended in assay media; and Daudi cell transfectants expressing IL-13R ⁇ 2.
  • 2.5 ⁇ 10 5 , 1.25 ⁇ 10 5 , 0.25 ⁇ 10 5 , and 0.05 ⁇ 10 5 effectors are plated in triplicate at 37° C. for 4 hours with 5 ⁇ 10 3 target cells in V-bottom microtiter plates (Costar, Cambridge, Mass.). After centrifugation and incubation, 100 ⁇ L aliquots of cell-free supernatant is harvested and counted. Percent specific cytolysis is calculated as:
  • Control wells contain target cells incubated in assay media.
  • Maximum 51 Cr release is determined by measuring the 51 Cr content of target cells lysed with 2% SDS. Criteria for clone selection is >25% specific lysis of IL-13R ⁇ 2+ Daudi transfectants at an E:T ratio of 5:1 and a ⁇ 10% lysis of parental Daudi at the same E:T ratio.
  • T cell clones genetically modified according to Example 5 to express the IL-13R zetakine chimeric immunoreceptor and HyTK are selected for:
  • Peripheral blood mononuclear cells are obtained from the patient by leukapheresis, preferably following recovery from initial resection surgery and at a time at least three weeks from tapering off steroids and/or their most recent systemic chemotherapy.
  • the target leukapheresis mononuclear cell yield is 5 ⁇ 10 9 and the target number of hygromycin-resistant cytolytic T cell clones is 25 with the expectation that at least five clones will be identified that meet all quality control parameters for ex-vivo expansion.
  • Clones are cryopreserved and patients monitored by serial radiographic and clinical examinations.
  • a reservoir-access device for delivering T cells to the tumor resection cavity.
  • the patient commences with T cell therapy.
  • the patient receives a target of at least four one-week cycles of therapy.
  • cell dose escalation proceeds from an initial dose on Day 0 of 10 7 cells, followed by 5 ⁇ 10 7 cells on Day 3 to the target-dose of 10 8 cells on Day 5.
  • Cycle 2 commences as early as one week from commencement of cycle 1.
  • Those patients demonstrating tumor regression with residual disease on MRI may have additional courses of therapy beginning no earlier than Week 7 consisting of repetition of Cycles 3 and 4 followed by one week of rest/restaging provided these treatments are well tolerated (max. toxicities ⁇ grade 3) until such time that disease progression or a CR is achieved based on radiographic evaluation.
  • Cell doses are at least a log less than doses given in studies employing intracavitary LAK cells (individual cell doses of up to 10 9 and cumulative cell numbers as high as 2.75 ⁇ 10 10 have been safety administered), ex vivo expanded TILs (up to 10 9 cells/dose reported with minimal toxicity) and allo-reactive lymphocyte (starting cell dose 10 8 with cumulative cell doses up to 51.5 ⁇ 10 8 ) delivered to a similar patient population 75-85 .
  • the rationale for the lower cell doses as proposed in this protocol is based on the increased in vitro reactivity/anti-tumor potency of IL-13 zetakine+ CTL clones compared to the modest reactivity profile of previously utilized effector cell populations.
  • Each infusion will consist of a single T cell clone.
  • the same clone will be administered throughout a patient's treatment course.
  • expanded clones are aseptically processed by washing twice in 50 cc of PBS then resuspended in pharmaceutical preservative-free normal saline in a volume that results in the cell dose for patient delivery in 2 mls.
  • T cells are instilled over 5-10 minutes.
  • a 2 ml PFNS flush will be administered over 5 minutes following T cells.
  • Response to therapy is assessed by brain MRI+/ ⁇ gandolinium, with spectroscopy.
  • T cells into glioma resection cavities typically consist of self-limited nausea and vomiting, fever, and transient worsening of existing neurological deficits. These toxicities can be attributed to both the local inflammation/edema in the tumor bed mediated by T cells in combination with the action of secreted cytokines. These side-effects typically are transient and less than grade II in severity. Should patients experience more severe toxicities it is expected that decadron alone or in combination with ganciclovir will attenuate the inflammatory process and ablate the infused cells. The inadvertent infusion of a cell product that is contaminated with bacteria or fungus has the potential of mediating serious or life-threatening toxicities.
  • Extensive pre-infusion culturing of the cell product is conducted to identify contaminated tissue culture flasks and minimize this possibility. On the day of re-infusion, gram stains of culture fluids, as well as, endotoxin levels are performed.
  • IL-13R ⁇ 2 Extensive molecular analysis for expression of IL-13R ⁇ 2 has demonstrated that this molecule is tumor-specific in the context of the CNS 44; 46; 48; 54 Furthermore, the only human tissue with demonstrable IL-13R ⁇ 2 expression appears to be the testis 42 . This tumor-testis restrictive pattern of expression is reminiscent of the growing number of tumor antigens (i.e. MAGE, BAGE, GAGE) expressed by a variety of human cancers, most notably melanoma and renal cell carcinoma 109-111 . Clinical experience with vaccine and adoptive T cell therapy has demonstrated that this class of antigens can be exploited for systemic tumor immunotherapy without concurrent autoimmune attack of the testis 112-114 .
  • MAGE tumor antigens
  • ganciclovir Side effects associated with therapy (headache, fever, chills, nausea, etc.) are managed using established treatments appropriate for the condition.
  • the patient receives ganciclovir if any new grade 3 or any grade 4 treatment-related toxicity is observed that, in the opinion of the treating physician, puts that patient at significant medical danger.
  • Parentally administered ganciclovir is dosed at 10 mg/kg/day divided every 12 hours. A 14-day course will be prescribed but may be extended should symptomatic resolution not be achieved in that time interval.
  • Treatment with ganciclovir leads to the ablation of IL-13 zetakine + HyTK + CD8 + CTL clones. Patients should be hospitalized for the first 72 hours of ganciclovir therapy for monitoring purposes.
  • immunosuppressive agents including but not limited to corticosteroids and cyclosporin may be added at the discretion of the treating physician. If toxicities are severe, decadron and/or other immunosuppressive drugs along with ganciclovir are used earlier at the discretion of the treating physician.
  • FIGS. 13 and 14 Additional DNA vectors are shown in FIGS. 13 and 14 .
  • Table I contains further information concerning the sequence of FIG. 13 . See FIG. 10 for a map of this vector.

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US13/046,518 US8324353B2 (en) 2001-04-30 2011-03-11 Chimeric immunoreceptor useful in treating human gliomas
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