EP2627782A2 - Marker sequences for systemic lupus erythematosus and the use thereof - Google Patents
Marker sequences for systemic lupus erythematosus and the use thereofInfo
- Publication number
- EP2627782A2 EP2627782A2 EP11782567.9A EP11782567A EP2627782A2 EP 2627782 A2 EP2627782 A2 EP 2627782A2 EP 11782567 A EP11782567 A EP 11782567A EP 2627782 A2 EP2627782 A2 EP 2627782A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- homo sapiens
- protein
- isoform
- seq
- lupus erythematosus
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
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Classifications
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6854—Immunoglobulins
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6834—Enzymatic or biochemical coupling of nucleic acids to a solid phase
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/106—Pharmacogenomics, i.e. genetic variability in individual responses to drugs and drug metabolism
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/158—Expression markers
Definitions
- the present invention relates to novel marker sequences for systemic lupus erythematosus and their diagnostic
- the invention relates to a diagnostic device containing such marker sequences for systemic lupus erythematosus,
- Protein biochips are gaining an increasing industrial
- Protein biochips require the necessary proteins to be available. In particular,
- the cDNA of a particular tissue in a bacterial or a eukaryotic expression vector, such as yeast, is cloned.
- the vectors used for the expression are generally characterized by the fact that they carry inducible promoters, with which the timing of protein expression can be controlled.
- expression vectors have sequences for so-called
- Affinity epitopes or proteins on the one hand for the specific detection of the recombinant fusion proteins by means of a directed against the affinity epitope
- Antibody on the other hand becomes the specific one
- antibody-presenting arrangements are also described (Lal et al (2002) Antibody arrays: An embryonic but growing technology, DDT, 7, 143-149, Kusnezow et al., (2003) Antibody microarrays: An evaluation of production parameters, Proteomics, 3, 254-264).
- the object of the present invention is to provide improved marker sequences and their diagnostic
- the invention relates to the use of
- marker sequences of the invention to or from a patient to be examined is determined.
- the marker sequences of the invention could by means of differential screening of samples and healthy
- systemic lupus erythematosus refers to a systemic autoimmune disease from the group of
- Serositis pleuritis or pericarditis
- Kidney involvement proteinuria> 0.5 g / d or cylinder
- haematological findings (haemolytic anemia, leuco-od.
- Diagnosis as certain (probable) (definition, for example, according to Pschyrembel, de Gruyter, 261st edition (2007), Berlin).
- Essential to the invention is that the samples are not taken from conventional blood banks, but from SLE patients
- HIV and HCV are negative and in particular have been tested for infectious diseases.
- the elaborate trial selection procedure allows e.g. a sufficient advantageous delineation of diseases with SLE-like symptoms. In this way false-positive results are excluded, also due to the strict bioinformatory evaluation (see examples).
- the production of the protein biochips by means of normalization of at least 1,000, preferably 2,000 different or more autoantigens of humans, which are not specific to the indication for systemic lupus erythematosus.
- autoantigens may e.g. from body fluids of patients of other autoimmune diseases, e.g. Pancreatic cancer, rheumatoid arthritis, prostate etc.
- the invention also relates to such indication-specific protein biochips according to the invention for the diagnosis of
- Normalized protein biochip proves to be particularly advantageous for the identification of the specific marker sequences according to the invention, since others are similar
- autoimmune relevant marker sequences can be excluded. This is contrary to the teaching of WO2003 / 090694.
- Intestinal bacteria are directed in humans. As a result, can advantageously with an improved signal / noise
- Ratio of new marker sequences can be identified.
- Marker sequences or 50 to 100 or more marker sequences to or from a patient to be examined.
- the marker sequences according to the invention can also be combined, supplemented or extended with known biomarkers for this indication.
- the determination of the marker sequences takes place outside the human body and the determination is made in an ex vivo / in vitro diagnosis.
- the invention relates to the use of marker sequences as diagnostics, wherein at least one marker sequence of a cDNA selected from the group SEQ 1-716 or in each case a protein coding therefor or in each case a partial sequence or fragment thereof.
- the invention relates to a method for the diagnosis of systemic lupus erythematosus, wherein a.) At least one marker sequence of a cDNA selected from the group SEQ 1-716 or a respective coding protein or a partial sequence or fragment thereof is applied to a solid support, and b.) with body fluid or
- Tissue extract of a patient is brought into contact and c.)
- the detection of an interaction of the body fluid or tissue extract with the marker sequences from a.) Is done.
- the invention also relates to diagnostics for
- the detection of such an interaction can, for example, by a probe, in particular by an antibody
- the invention also has the object of providing a diagnostic device or an assay, in particular a protein biochip, which permits diagnosis or examination for systemic lupus erythematosus.
- the invention relates to a method for
- Stratify in particular for risk stratification and / or therapy control of a patient with systemic lupus erythematosus, wherein at least one marker sequence of a cDNA selected from the group SEQ 1-716 or in each case a protein coding therefor is determined on a patient to be examined.
- Therapy control also includes the classification of
- Diagnosis in the sense of this invention means the positive determination of the systemic lupus erythematosus by means of the marker sequences according to the invention and the assignment of the patients to the disease of systemic lupus erythematosus.
- diagnosis includes medical diagnostics and related investigations, in particular in vitro diagnostics and Laboratory diagnostics, also proteomics and nucleic acid blots
- diagnosis also includes the
- Stratification (or stratification) or therapy control in the sense of this invention means that the method according to the invention allows decisions for the treatment and therapy of the patient, be it hospitalization of the patient, Use, effect and / or dosage of one or more drugs, a therapeutic measure or the
- the term "stratification" includes in particular the
- patient is understood to mean any subject - human or mammal - with the proviso that the subject is on systemic lupus erythematosus
- marker sequences in the sense of this invention means that the cDNA or the respective polypeptide or protein obtainable therefrom are significant for systemic lupus erythematosus
- the cDNA or the respective polypeptide or protein obtainable therefrom can be a
- erythematosus e.g., antigen (epitope) / antibody (paratope) interaction
- Marker sequences is detected. Such an interaction is for example a bond, in particular a binding substance to at least one marker sequence according to the invention or in the case of a cDNA hybridization with a suitable substance under selected conditions, in particular stringent
- Hybridization conditions are: hybridization in 4 x SSC at 65 ° C (alternatively in 50% formamide and 4X SSC at 42 ° C), followed by several washes in 0.1 x SSC at 65 ° C for a total of about one hour.
- An example of less stringent hybridization conditions is hybridization in 4 x SSC at 37 ° C, followed by several washes in 1 x SSC at room temperature.
- Such substances are part of a body fluid according to the invention, in particular blood, whole blood, blood plasma, blood serum, patient serum, urine, cerebrospinal fluid,
- Synovial fluid or a tissue extract of the patient Synovial fluid or a tissue extract of the patient.
- the marker sequences according to the invention may be present in a significantly higher or lower expression rate or concentration, which indicates systemic lupus erythematosus. This can be done by means of proteomics or
- Nucleic acid blots the relative expression rates ill / healthy of the marker sequences according to the invention for systemic lupus erythematosus are determined.
- the marker sequences have a recognition signal which is addressed to the substance to be bound (for example antibodies,
- the recognition signal is preferably an epitope and / or paratope and / or hapten and, for a cDNA, a hybridization or hybridization protein
- the marker sequences of the invention are also possible.
- the invention also relates to the full-length sequences of the markers according to the invention and indeed as defined in Table A on the known database entry, hereinafter called SEQ -716a (cDNA).
- SEQ 1-716 according to the invention again represent partial sequences, at least with high homology.
- the specific ones are identical to SEQ 1-716 according to the invention.
- marker sequences SEQ 1-716 are in accordance with the invention.
- marker sequences also include such modifications of the cDNA sequence and the corresponding
- Amino acid sequence such as chemical modification, such as
- marker sequences In particular, those partial sequences which have an identity of 95%, 90%, in particular 80% or 70% with the marker sequences according to the invention.
- Partial sequences are also those sequences having 50 to 100 nucleotides, 70-120 nucleotides of a sequence of SEQ 1-716, or peptides obtainable therefrom.
- Marker sequences are functionally defined and include those sequences which have the same inventive diagnostic function.
- Marker sequence can be represented in different amounts in one or more areas on a solid support. This allows a variation of the sensitivity.
- the regions may each comprise a total of marker sequences, i. a sufficient number of different marker sequences, in particular 2 to 5 or 10 or more and optionally further nucleic acids and / or proteins, in particular biomarkers.
- Biomarkers Further preferred are more than 2,500, more preferably 10,000 or more different or the same
- Proteins especially biomarkers.
- Another object of the invention relates to an array of marker sequences containing at least one marker sequence a cDNA selected from the group SEQ 1-716 or in each case a protein coding therefor.
- the group SEQ 1-716 or in each case a protein coding therefor.
- “arrangement” synonymously means “array” and insofar as this "array” is used to identify substances on marker sequences, this is to be understood as meaning an “assay” or a diagnostic device.
- the arrangement is designed such that those represented on the assembly
- Marker sequences are in the form of a grid on a solid support. Furthermore, such arrangements are preferred which include a high density array of protein binders
- Such high density spotted assemblies are disclosed, for example, in WO 99/57311 and WO 99/57312, and may be advantageously used in a robotic automated high throughput method.
- test or diagnostic device also includes such
- Embodiments of a device such as ELISA, bead-based assay, line assay, Western blot, immunochromatographic
- Invention is the systematic arrangement of proteins on a solid support.
- the marker sequences of the assembly are fixed to a solid support, but preferably spotted or immobilized imprinted, ie applied reproducible.
- One or more marker sequences can be duplicated in the totality of all
- Marker sequences are present and available in different quantities based on a spot. Furthermore, the
- Marker sequences on the solid support may be standardized (e.g., by serial dilution series of e.g.
- the invention relates to an assay or protein biochip consisting of an array containing marker sequences according to the invention.
- the marker sequences are present as clones.
- Such clones can be obtained, for example, by means of a cDNA expression library according to the invention (Büssow et al., 1998 (supra)).
- such expression libraries become
- Obtained marker sequences are obtained. These expression vectors preferably contain inducible promoters. The induction of
- Expression can e.g. by means of an inductor, such as IPTG.
- IPTG inductor
- Suitable expression vectors are described in Terpe et al. (Terpe T Appl Microbiol Biotechnol 2003 Jan; 60 (5): 523-33).
- Expression libraries are known to the person skilled in the art, these can be prepared according to standard works, such as Sambrook et al., Molecular Cloning, Laboratory Handbook, 2nd edition (1989), CSH press, Cold Spring Harbor, New York Further preferred are such expression libraries
- tissue specific eg human tissue, in particular human organs
- expression libraries are also included according to the invention, which can be obtained by exon trapping. Instead of expression library can be spoken synonymously from an expression bank.
- protein biochips or corresponding expression libraries which have no redundancy (so-called: Uniclone® library) and can be prepared, for example, according to the teachings of WO 99/57311 and WO 99/57312. These preferred Uniclone libraries have a high content of non-defective, fully expressed proteins of a cDNA expression library.
- the clones may not be such as transformed bacteria, recombinant phage or transformed cells of mammals, insects, fungi, yeasts or plants.
- the clones are fixed on a solid support, spotted or immobilized.
- the invention relates to an arrangement, wherein the
- Marker sequences are present as clones.
- the marker sequences may be in the form of a fusion protein in the particular form
- At least one affinity epipope or "tag” contains.
- the tag may be one such as c-myc, His-tag, Arg-tag, FLAG, alkaline phosphatase, V5 tag, T7 tag or Strep tag, HAT tag, NusA, S-tag, SBP tag , Thioredoxin, DsbA, a fusion protein, preferably a cellulose-binding one
- solid support includes embodiments such as a filter, a membrane, a magnetic or fluorophore-labeled bead
- Silicon wafer, glass, metal, plastic, a chip, a mass spectrometric target or a matrix Silicon wafer, glass, metal, plastic, a chip, a mass spectrometric target or a matrix.
- a filter is preferred according to the invention.
- the filter is PVDF, nitrocellulose or nylon (e.g., Immobilon P Millipore, Protran Whatman, Hybond N + Amersham).
- this corresponds to a grid having the order of a microtiter plate (8-12 wells strips, 96 wells, 384 wells or more), a silicon wafer, a chip, a mass spectrometric target or a matrix.
- the invention relates to an assay or protein biochip for identifying and
- inventive arrangement or assay with a.) At least one substance to be examined is brought into contact and b.) A binding success is detected.
- the invention relates to a method for identifying and characterizing a substance for systemic lupus erythematosus, characterized in that a
- inventive arrangement or assay with a.) At least one substance to be examined is brought into contact and b.) A binding success is detected.
- the substance to be tested may be any native or non-native biomolecule, a synthetic chemical
- protein to marker sequence e.g., protein to marker sequence
- Antigen / antibody or corresponding "means for detecting the binding success" can, for example, by means of
- reporter enzymes such as alkaline
- a readout is e.g. by means of a microarray laser scanner, a CCD camera or visually.
- the invention relates to a drug / drug or prodrug developed for systemic lupus erythematosus and obtainable by the use of the assay or protein biochip according to the invention. Therefore, the invention also relates to the use of an inventive arrangement or an assay for screening agents for systemic lupus erythematosus.
- the invention also relates to a target for the treatment and therapy of
- Systemic lupus erythematosus each selected from the group SEQ 1-716 or in each case a protein coding therefor.
- the invention also relates to the use of the invention
- Marker sequences preferably in the form of an arrangement, as
- Affinity material for performing an apheresis or iwS. a blood wash wherein substances from body fluids of a patient with systemic lupus erythematosus, such as blood or plasma, bind to the marker sequences according to the invention and consequently the body fluid can be selectively withdrawn.
- Ten or more patient samples were individually screened against a cDNA expression library.
- the systemic lupus erythematosus-specific expression clones were determined by comparison with ten or more healthy samples.
- the identity of the marker sequences was determined by DNA sequencing.
- FIG. 1 shows the differential screening between two protein biochips from in each case one cDNA expression bank of a patient and one healthy subject.
- Differential clones are detected by fluorescence labeling and evaluated bioinformatorisch.
- biomarker identification various bioinformatic analyzes are carried out. For each serum, microarray reactivities against about 2000
- Intensity data performed.
- an internal standard is used, which is spotted on each chip. Since a p-value is calculated for each antigen, methods for correcting multiple testing are used. As a very conservative approach, a Bonferroni correction is performed and, in addition, the less restrictive False Discovery Rate (FDR) is calculated according to Benjamini & Hochberg.
- FDR False Discovery Rate
- the data are used to classify the sera.
- different multivariate methods are used. These are methods from the statistical
- Threshold method which is suitable for both classification and visual representation of the data.
- gil4501867 aconitase 2 precursor [Homo sapiens]
- gil4501885 beta actin [Homo sapiens]
- gil4501887 actin gamma 1 propeptide [Homo sapiens]
- solute carrier family 25 mitochondria carrier; adenine nucleotide translocator, member 4 gil55749577
- gill56071462 solute carrier family 25, member A6 [Homo sapiens]
- gill78557739 complement component 4B preproprotein [Homo sapiens]
- gill 19627240 cyclin-dependent kinase inhibitor 2C (pI8, inhibits CDK4), isoform CRA_b [Homo sapiens] gil56786147 cysteine dioxygenase, type I [Homo sapiens]
- gil5031635 cofilin 1 (non-muscle) [Homo sapiens]
- gil21536286 brain creatine kinase [Homo sapiens] gil4502847 cold inducible RNA binding protein [Homo sapiens]
- gill4917109 adaptor-related protein complex 2 mu 1 subunit isoform a [Homo sapiens] gil4557471 adaptor-related protein complex 1, sigma 1 subunit [Homo sapiens]
- gil4502981 cytochrome c oxidase subunit IV isoform 1 precursor [Homo sapiens]
- gil4503049 cysteine-rich protein 2 [Homo sapiens]
- gil4503051 collapsin response mediator protein 1 isoform 2 [Homo sapiens]
- gil4758138 DEAD (Asp-Glu-Ala-Asp) box polypeptide 5 [Homo sapiens]
- gil4503481 eukaryotic translation elongation factor 1 gamma [Homo sapiens]
- gil4503529 eukaryotic translation Initiation factor 4A isoform 1 [Homo sapiens]
- gil4503659 ubiquitin-like protein fubi and ribosomal protein S30 precursor [Homo sapiens] gil67089147 farnesyl diphosphate farnesyltransferase 1 [Homo sapiens]
- gil213417614 fibroblast growth factor 13 isoform 3 [Homo sapiens]
- gil4503711 fibroblast growth factor receptor 3 isoform 1 precursor [Homo sapiens] gil4503727 FK506 binding protein 3, 25kDa [Homo sapiens] gil56682959 ferritin, heavy polypeptide 1 [Homo sapiens]
- GABA gamma-aminobutyric acid
- gil4504111 growth factor receptor-bound protein 2 isoform 1 [Homo sapiens]
- gill54146191 heat shock protein 90kDa alpha (cytosolic), class A member 1 isoform 2 [Homo sapiens] gil31542947 chaperonin [Homo sapiens]
- gill2545395 islet cell autoantigen 1 [Homo sapiens]
- gil28178832 isocitrate dehydrogenase 2 (NADP +), mitochondrial precursor [Homo sapiens] gil28178821 isocitrate dehydrogenase 3, beta subunit isoform a precursor [Homo sapiens] gil4504619 insulin-like growth factor binding protein 7 [Homo sapiens]
- gil4758648 kinesin family member 5B [Homo sapiens]
- gill 16829964 KiSS-1 metastasis-suppressor [Homo sapiens]
- gil9845502 ribosomal protein SA [Homo sapiens]
- gill53945728 microtubule-associated protein 1B [Homo sapiens]
- microtubule-associated protein tau isoform 4 [Homo sapiens]
- myeloid / lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, gil57222568
- gil5031931 nascent polypeptide-associated complex alpha subunit isoform b [Homo sapiens]
- NM23B protein expressed in [Homo sapiens]
- gil34098946 nuclease sensitive element binding protein 1 [Homo sapiens]
- gil71361682 nuclear mitotic apparatus protein 1 [Homo sapiens]
- gil4505621 prostatic binding protein [Homo sapiens]
- gil22202633 prefoldin subunit 5 isoform alpha [Homo sapiens]
- gil20149543 placental growth factor vascular endothelial growth factor-related protein
- gil5453898 protein peptidyl prolyl cis / trans isomerase
- NIMA interacting 1 [Homo sapiens]
- gil205360954 polycystin 1 isoform 1 precursor [Homo sapiens]
- gill56616275 Polymerase (DNA directed), delta 1, catalytic subunit 125kDa [Homo sapiens] gill 10618253 mitochondrial DNA-directed RNA polymerase precursor [Homo sapiens]
- gil93277122 RNA binding motif protein 4 [Homo sapiens]
- gill56416009 regulator of G-protein signaling 16 [Homo sapiens] gil4506649 ribosomal protein L3 isoform a [Homo sapiens] gill6579885 ribosomal protein L4 [Homo sapiens]
- gil4506633 ribosomal protein L31 isoform 1 [Homo sapiens] gill6117791 ribosomal protein L35a [Homo sapiens]
- gil4506725 ribosomal protein S4 X-linked X isoform [Homo sapiens] gil4506727 ribosomal protein S4, Y-linked 1 Y isoform [Homo sapiens] gill 3904870 ribosomal protein S5 [Homo sapiens]
- solute carrier family 25 mitochondria carrier; citrate transporter
- member 1 precursor Homo gil21389315
- gil4507171 secreted protein, acidic, cysteine-rich [Homo sapiens]
- gil 149999611 signal recognition particle 14kDa homologous Alu RNA binding protein
- gill5208660 tripartite motif protein 21 homologous Alu RNA binding protein
- gill08796056 TROVE domain family member 2 isoform 1 [Homo sapiens]
- gil4507239 signal sequence receptor, beta precursor [Homo sapiens]
- gil29540543 sulfotransferase family, cytosolic, 1A, phenolic-preferring, member 1 isoform b [homo sapiens] gil92859638 synaptotagmin V [homo sapiens]
- gil4507645 triosephosphate isomerase 1 [Homo sapiens]
- gil4507677 heat shock protein 90kDa beta, member 1 [Homo sapiens]
- gil6005942 valosin-containing protein [Homo sapiens]
- gil4507961 zinc finger protein 36 C3H type, homologous [Homo sapiens]
- gil4503515 eukaryotic translation Initiation factor 3, subunit 3 gamma, 40kDa [Homo sapiens]
- gil4507285 syntaxin 10 [Homo sapiens]
- gil46909598 a disintegrin and metalloproteinase domain 15 isoform 5 preproprotein [Homo sapiens] gil4505229 Fas-associated via death domain [Homo sapiens]
- gil4759276 RNA U3 small nucleolar interacting protein 2 [Homo sapiens]
- gill95927015 phosphatidylinositol transfer protein, membrane-associated isoform a [Homo sapiens]
- gill 16256445 nuclear receptor co-repressor 2 isoform 2 [Homo sapiens]
- Rho GTPase activating protein RICH2 [Homo sapiens]
- gill94294519 nuclear receptor subfamily 1 group H, member 3 isoform c [Homo sapiens] gil65301139 ATPase, class II, type 9A [Homo sapiens]
- gil6912540 nucleotide binding protein 2 (MinD homologue, E. coli) [Homo sapiens]
- TNF receptor-associated protein 1 [Homo sapiens]
- RecName: Full Major facilitator superfamily domain-containing protein 10; AltName: gil74735668
- gil5031669 cyclin-dependent kinase 2 associated protein 2 [Homo sapiens]
- G protein guanine nucleotide binding protein
- beta polypeptide 2-like 1 guanine nucleotide binding protein
- gil5454064 RNA binding motif protein 14 Homo sapiens
- gil5453595 adenylyl cyclase-associated protein [Homo sapiens]
- gil5454166 vesicle transport through interaction with t-SNAREs 1B [Homo sapiens]
- gil36287060 K (lysine) acetyltransferase 5 isoform 3 [Homo sapiens]
- RNA-binding protein 1 isoform 1 [Homo sapiens]
- gil6005764 GABA (A) receptor-associated protein [Homo sapiens]
- gil20336290 DEAH Adi-Glu-Ala-His box polypeptides 30 isoform 2 [Homo sapiens]
- RNA binding protein autoantigenic, hnRNP-associated with lethal yellow
- gil82659109 retinoblastoma-associated factor 600 [Homo sapiens]
- gil4507975 zinc finger protein 345 [Homo sapiens]
- gil7657196 zinc finger protein 330 [Homo sapiens]
- gil7657381 PRP19 / PS04 pre-mRNA processing factor 19 homolog [Homo sapiens]
- gil54607124 RNA binding motif protein 15B [Homo sapiens]
- glioma tumor suppressor candidate region protein 2 (AF182076_1) [Homo sapiens]
- gil7305503 stomatin (EPB72) -like 2 [Homo sapiens]
- gil7705716 nitric oxide synthase interacting protein [Homo sapiens]
- gill89083821 inhibitor of growth family member 4 isoform 9 [Homo sapiens]
- gill56142184 ankyrin repeat domain 39 [Homo sapiens]
- gil75677349 poly (A) binding protein interacting protein 2 [Homo sapiens]
- gil7705433 eukaryotic translation Initiation factor 3 subunit 6 interacting protein [Homo sapiens]
- gil7705294 actin-like 6B [Homo sapiens]
- gil37537687 zinc finger protein 444 [Homo sapiens]
- gil7020625 unnamed protein product [Homo sapiens]
- gil8922328 RNA binding motif protein 22 [Homo sapiens]
- gill7999541 vacuolar protein sorting 35 [Homo sapiens]
- gil57863279 Meisl myeloid ecotropic viral Integration site 1 homologue 3 isoform 2 [Homo sapiens]
- gil94536838 poly (ADP-ribose) polymerase family, member 6 [Homo sapiens]
- gil70778869 invasion inhibitory protein 45 [Homo sapiens]
- gil 130978962 adrenocortical dysplasia homologous isoform 2 [Homo sapiens]
- gil30581160 ganglioside-induced differentiation-associated protein 1-like 1 [Homo sapiens]
- gill3128992 hypothetical protein MGC2803 [Homo sapiens]
- glial cell differentiation regulator [Homo sapiens]
- gill46198654 zinc finger protein 768 [Homo sapiens]
- gil 13654276 queuine tRNA-ribosyltransferase 1 [Homo sapiens]
- gil42734379 THAP domain containing, apoptosis associated protein 3 [Homo sapiens]
- gil55742736 zinc finger protein 700 [Homo sapiens]
- gil217416379 heterogeneous nuclear ribonucleoprotein L-like isoform 2 [Homo sapiens]
- gil34878735 F-box protein 44 isoform 1 [Homo sapiens]
- HGFL protein isoform 2 [Homo sapiens]
- gil22035616 oxysterol-binding protein-like protein 7 [Homo sapiens]
- gil30520320 ring finger protein 166 [Homo sapiens]
- gil28274701 zinc finger protein 511 [Homo sapiens]
- gill33922582 zinc finger protein 358 [Homo sapiens]
- gill90341093 fibroblast growth factor binding protein 3 [Homo sapiens]
- gill 10681708 zinc finger protein 579 [Homo sapiens]
- gil22749235 zinc finger protein 709 [Homo sapiens]
- RNA III DNA directed polypeptides H (22.9kD) isoform a [Homo sapiens] gil21699088 zinc finger protein 627 [Homo sapiens]
- gil30026034 solute carrier family 35 member B2 [Homo sapiens]
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- Hematology (AREA)
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Abstract
Description
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11782567.9A EP2627782A2 (en) | 2010-10-12 | 2011-10-12 | Marker sequences for systemic lupus erythematosus and the use thereof |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10187316A EP2441848A1 (en) | 2010-10-12 | 2010-10-12 | Marker sequences for systematic lupus erythematodes and use of same |
| EP11782567.9A EP2627782A2 (en) | 2010-10-12 | 2011-10-12 | Marker sequences for systemic lupus erythematosus and the use thereof |
| PCT/EP2011/067842 WO2012049225A2 (en) | 2010-10-12 | 2011-10-12 | Marker sequences for systemic lupus erythematosus and the use thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2627782A2 true EP2627782A2 (en) | 2013-08-21 |
Family
ID=43533355
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP10187316A Withdrawn EP2441848A1 (en) | 2010-10-12 | 2010-10-12 | Marker sequences for systematic lupus erythematodes and use of same |
| EP11782567.9A Withdrawn EP2627782A2 (en) | 2010-10-12 | 2011-10-12 | Marker sequences for systemic lupus erythematosus and the use thereof |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP10187316A Withdrawn EP2441848A1 (en) | 2010-10-12 | 2010-10-12 | Marker sequences for systematic lupus erythematodes and use of same |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US20130303395A1 (en) |
| EP (2) | EP2441848A1 (en) |
| WO (1) | WO2012049225A2 (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2608315C (en) * | 2005-05-13 | 2014-08-05 | Centre National De La Recherche Scientifique | Use of a new gene coding for a new member of the mcm2-8 family in pharmaceutical compositions |
| AR086673A1 (en) * | 2011-06-06 | 2014-01-15 | Baylor Res Inst | IMPROVED ANSWERS BY LES-DC OF B-CELLS THAT SECRET IgG AND IgA |
| US10060911B2 (en) | 2011-08-19 | 2018-08-28 | Protagen Aktiengesellschaft | Method for diagnosis of high-affinity binders and marker sequences |
| WO2015118184A1 (en) | 2014-02-10 | 2015-08-13 | Protagen Ag | Marker sequences for diagnosing and stratifying sle patients |
| WO2017168014A1 (en) * | 2016-04-02 | 2017-10-05 | Protagen Ag | Marker sequences for rheumatoid arthritis |
| US12203933B2 (en) | 2018-08-15 | 2025-01-21 | Mayo Foundation For Medical Education And Research | Methods and materials for identifying and treating membranous nephropathy |
| CN110873797B (en) * | 2019-12-09 | 2021-07-30 | 四川大学华西医院 | Use of FKBP8 autoantibody detection reagent in the preparation of lung cancer screening kit |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1073771T1 (en) | 1998-04-30 | 2002-06-13 | Max-Planck-Gesellschaft Zur Foerderung Der Wissenschaften E.V. | NEW METHOD FOR SELECTION OF CLONES OF AN EXPRESSION LIBRARY BY MEANS OF "REARRAYING" |
| AU770540B2 (en) | 1998-04-30 | 2004-02-26 | Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V. | Novel method for the identification of clones conferring a desired biological property from an expression library |
| US6537968B1 (en) * | 2000-07-24 | 2003-03-25 | Alphamed Pharmaceuticals Corp | Treatment of lupus erythematosus |
| US20030148298A1 (en) * | 2001-04-03 | 2003-08-07 | O''toole Margot | Methods for diagnosing and treating systemic lupus erythematosus disease and compositions thereof |
| US6905827B2 (en) * | 2001-06-08 | 2005-06-14 | Expression Diagnostics, Inc. | Methods and compositions for diagnosing or monitoring auto immune and chronic inflammatory diseases |
| AU2002367732A1 (en) * | 2001-10-31 | 2003-09-09 | Children's Hospital Medical Center | Method for diagnosis and treatment of rheumatoid arthritis |
| CA2485968A1 (en) * | 2002-05-16 | 2004-06-03 | Vanderbilt University | Method for predicting autoimmune diseases |
| DE102007062847A1 (en) * | 2007-12-21 | 2009-12-31 | Protagen Ag | Marker sequences for neurodegenerative diseases and their use |
| WO2012031122A2 (en) * | 2010-09-03 | 2012-03-08 | Immport Therapeutics, Inc. | Methods and compositions for the diagnosis and treatment of cancer and autoimmune disorders |
-
2010
- 2010-10-12 EP EP10187316A patent/EP2441848A1/en not_active Withdrawn
-
2011
- 2011-10-12 US US13/879,149 patent/US20130303395A1/en not_active Abandoned
- 2011-10-12 WO PCT/EP2011/067842 patent/WO2012049225A2/en not_active Ceased
- 2011-10-12 EP EP11782567.9A patent/EP2627782A2/en not_active Withdrawn
Non-Patent Citations (2)
| Title |
|---|
| None * |
| See also references of WO2012049225A2 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2012049225A2 (en) | 2012-04-19 |
| EP2441848A1 (en) | 2012-04-18 |
| WO2012049225A3 (en) | 2012-06-21 |
| US20130303395A1 (en) | 2013-11-14 |
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