EP2201132A2 - Séquences de marqueurs de la sclérose en plaques et leur utilisation - Google Patents

Séquences de marqueurs de la sclérose en plaques et leur utilisation

Info

Publication number
EP2201132A2
EP2201132A2 EP08828970A EP08828970A EP2201132A2 EP 2201132 A2 EP2201132 A2 EP 2201132A2 EP 08828970 A EP08828970 A EP 08828970A EP 08828970 A EP08828970 A EP 08828970A EP 2201132 A2 EP2201132 A2 EP 2201132A2
Authority
EP
European Patent Office
Prior art keywords
marker sequences
multiple sclerosis
case
marker
diagnosis
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.)
Ceased
Application number
EP08828970A
Other languages
German (de)
English (en)
Inventor
Jens Beator
Angelika LÜKING
Axel Kowald
Helmut E. Meyer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Protagen GmbH
Original Assignee
Protagen GmbH
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Protagen GmbH filed Critical Protagen GmbH
Priority to EP16192464.2A priority Critical patent/EP3147663A2/fr
Priority to EP16164136.0A priority patent/EP3070473A2/fr
Priority to EP14164521.8A priority patent/EP2884279A3/fr
Publication of EP2201132A2 publication Critical patent/EP2201132A2/fr
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/564—Immunoassay; Biospecific binding assay; Materials therefor for pre-existing immune complex or autoimmune disease, i.e. systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, rheumatoid factors or complement components C1-C9
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2800/00—Detection or diagnosis of diseases
    • G01N2800/28—Neurological disorders
    • G01N2800/285—Demyelinating diseases; Multipel sclerosis

Definitions

  • the present invention relates to novel marker sequences for multiple sclerosis and their diagnostic use, including a method for screening potential drugs for multiple sclerosis by means of these marker sequences. Furthermore, the invention relates to a diagnostic device containing such marker sequences for multiple sclerosis, in particular a protein biochip and its use.
  • Protein biochips are gaining increasing industrial importance in analytics and diagnostics as well as in pharmaceutical development. Protein biochips have become established as screening tools.
  • cDNA of a particular tissue in a bacterial or a eukaryotic expression vector, such as yeast is cloned.
  • the ones used for the expression Vectors are generally characterized by carrying inducible promoters that control the timing of protein expression.
  • expression vectors have sequences for so-called affinity epitopes or proteins, which on the one hand allow the specific detection of the recombinant fusion proteins by means of an antibody directed against the affinity epitope, on the other hand, the specific purification via affinity chromatography (IMAC) allows.
  • affinity epitopes or proteins which on the one hand allow the specific detection of the recombinant fusion proteins by means of an antibody directed against the affinity epitope, on the other hand, the specific purification via affinity chromatography (IMAC) allows.
  • IMAC affinity chromatography
  • 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).
  • indication-specific diagnostic devices such as a protein biochip.
  • the object of the present invention is therefore the provision of marker sequences and their diagnostic use.
  • the invention relates to the use of marker sequences for the diagnosis of multiple sclerosis, wherein at least one marker sequence of a cDNA selected from the group SEQ 1-395 or in each case a protein coding therefor or in each case a partial sequence or fragment thereof (hereinafter: marker sequences according to 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 from healthy volunteers with
  • Patient samples are identified with multiple sclerosis.
  • MS multiple sclerosis
  • encephalomyelitis disseminata encephalomyelitis disseminata
  • At least 2 to 5 or 10, preferably 30 to 50 marker sequences or 50 to 100 or more marker sequences are determined on or from a patient to be examined.
  • the marker sequences of SEQ 1-20 are particularly preferred, the marker sequences SEQ 21-50 are preferred and furthermore preferred are the marker sequences SEQ 51-100.
  • the marker sequences according to the invention can also be combined, supplemented, fused or extended with known biomarkers for this indication.
  • the determination of the marker sequences takes place outside the human body and the determination takes place in an ex vivo / in vitro diagnosis.
  • the invention relates to the use of marker sequences as diagnostic agents, wherein at least one marker sequence of a cDNA selected from the group SEQ 1-395 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 multiple sclerosis, wherein a.) At least one marker sequence of a cDNA selected from the group SEQ 1 - 395 or a respective coding protein or a partial sequence or fragment thereof is applied to a solid support and b .) is brought into contact with body fluid or tissue extract of a patient and c.) the detection of an interaction of the body fluid or tissue extract with the marker sequences from a.).
  • the invention also relates to diagnostics for
  • the detection of such an interaction can be carried out for example by a probe, in particular by an antibody.
  • the invention also relates to the task of providing a diagnostic device or an assay, in particular a protein biochip, which allows a diagnosis or examination for multiple sclerosis.
  • the invention relates to a method for stratifying, in particular for risk stratification and / or therapy control of a patient with multiple sclerosis, wherein at least one marker sequence of a cDNA selected from the group SEQ 1 - 395 or a protein coding therefor is determined on a patient to be examined.
  • therapy control also includes the classification of patients into responders and non-responders with regard to a therapy or its course of therapy.
  • Diagnosis in the sense of this invention means the positive determination of multiple sclerosis by means of the marker sequences according to the invention as well as the assignment of the patients to multiple sclerosis.
  • diagnosis encompasses medical diagnostics and related thereto
  • diagnosis also includes the differential diagnosis of multiple sclerosis by means of the marker sequences according to the invention and the prognosis of multiple sclerosis.
  • Stratification also: stratification or therapy control
  • diagnosis 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 monitoring of a course of disease as well as the course of therapy or etiology or classification of a disease, for example into a new or existing subtype or the differentiation of diseases and their patients.
  • the term "stratification" includes in particular the
  • patient means any subject - human or mammal - with the proviso that the subject is being examined for multiple sclerosis.
  • marker sequences in the sense of this invention means that the cDNA or the respective polypeptide or protein obtainable therefrom are significant for multiple sclerosis
  • the cDNA or the respectively obtainable polypeptide or protein may interact with substances from the body fluid or tissue extract of a
  • "at least one marker sequence of a cDNA selected from the group SEQ 1-395 or in each case a protein coding therefor or in each case a subsequence or” means having multiple sclerosis Fragment thereof is determined on a patient to be examined "that an interaction between the body fluid or tissue extract of a patient and the marker sequences according to the invention is detected.
  • Such an interaction is eg a bond, in particular a binding substance on at least one marker sequence according to the invention or in the case of a cDNA the hybridization with a suitable substance under selected conditions, in particular stringent conditions (eg as defined in J. Sambrook, EF Fritsch, T. Maniatis (1989), Molecular cloning: A laboratory manual, 2nd Edition, CoId Spring Habor Laboratory Press, CoId Spring Habor, USA or Ausubel , "Current Protocols in
  • An example of stringent hybridization conditions is: hybridization in 4 x SSC at 65 ° C (alternatively in 50% formamide and 4 X SSC at 42 ° C) by several washes in 0.1 x SSC at 65 0 C for a total of about one hour.
  • an example of low stringency hybridization conditions is hybridization in 4 x SSC at 37 ° C, followed by several washing steps in 1 x SSC at room temperature. Such substances are According to the invention part of a
  • Body fluid in particular blood, whole blood, blood plasma, blood serum, patient serum, urine, cerebrospinal fluid, 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 points to multiple sclerosis.
  • the relative expression rates ill / healthy of the marker sequences according to the invention for multiple sclerosis are determined by means of proteomics or nucleic acid blots.
  • the marker sequences have, in another embodiment of the invention, a recognition signal which is addressed to the substance to be bound (e.g., antibody, nucleic acid).
  • the recognition signal for a protein is preferably an epitope and / or paratope and / or hapten and, for a cDNA, a hybridization or binding region.
  • the marker sequences according to the invention are the subject of Table A and can by the respective cited Database entry (also via Internet: http://www.ncbi.nlm.nih.gov/) can be clearly identified (see Table A: there Accession No.).
  • the marker sequences also include such modifications of the cDNA sequence and the corresponding amino acid sequence, such as chemical modification, such as citrullination, acetylation, phosphorylation, glycosylation or polyA strand and other modifications known to those skilled in the art.
  • partial sequences or fragments of the marker sequences according to the invention are also included.
  • the respective marker sequence may be represented in different amounts in one or more regions on a solid support. This allows a variation of the sensitivity.
  • the regions may each comprise a total of marker sequences, i.
  • marker sequences in particular 2 to 5 or 10 or more and optionally further nucleic acids and / or proteins, in particular biomarkers.
  • at least 96 to 25,000 (numerically) or more are preferred from different or identical marker sequences and further nucleic acids and / or proteins, in particular biomarkers.
  • more than 2,500, more preferably 10,000 or more different or identical marker sequences and, if appropriate, further nucleic acids and / or proteins, in particular biomarkers are more than 2,500, more preferably 10,000 or more different or identical marker sequences and, if appropriate, further nucleic acids and / or proteins, in particular biomarkers.
  • Another object of the invention relates to an array of marker sequences containing at least one marker sequence of a cDNA selected from the group SEQ 1 - 395 or in each case a protein coding therefor.
  • “arrangement” means synonymously “array ⁇ and insofar as this" array "is used to identify substances on marker sequences, this is to be understood as an” assay "or diagnostic device. Further, such arrangements are preferred which allow a high density array of protein binders and spotting the marker sequences, Such high density spotted arrangements are described, for example, in WO 99/57311 and WO 99/57312, and may be advantageously used in a robotic automated high-throughput process.
  • the term "assay” or diagnostic device also encompasses such embodiments of a device as ELISA (eg individual wells of a microtiter plate are coated with the marker sequences of the invention or combinations of marker sequences, optionally robotically supported in the individual wells of the microtiter plate
  • ELISA eg individual wells of a microtiter plate are coated with the marker sequences of the invention or combinations of marker sequences, optionally robotically supported in the individual wells of the microtiter plate
  • diagnostic ELISA kits from Phadia or Multiplex ELISA kits "Searchlight” from Pierce / Thermo Fisher Scientific
  • bead-based assay are coated with marker sequences / combinations of marker sequences.
  • the patient sample is incubated with this bead population and bound (auto) antibodies are detected by means of another fluorescence-labeled secondary antibody / detection reagent by measuring the fluorescence, eg Borrelia IgG kit or Athena Multilyte from the company Multimetrix), Line Assay (Mar kersequences or combinations of marker sequences are robotically immobilized on membranes which are coupled to the Patient sample to be examined / incubated; Example "Euroline ⁇ " from Euroimmun AG), Western blot (example "Euroline-WB ⁇ " from Euroimmun AG), immunochromatographic methods (eg lateral flow immunoassays, marker sequences / combinations of marker sequences are applied to test strips (membranes, US Pat. No. 5,714,389) immobilized, for example, One Step HBsAg Test Device from Acon Laboratories) or similar immunological single or multiplex detection methods.
  • fluorescence eg Borrelia IgG kit or Athena Multily
  • the marker sequences of the assembly are fixed to a solid support, but preferably spotted or immobilized even printed, i. applied reproducibly.
  • One or more marker sequences may be present several times in the totality of all marker sequences and be present in different amounts relative to one spot. Further, the marker sequences may be standardized on the solid support (e.g., by serial dilution series of, e.g., human globulins as internal calibrators for data normalization and quantitative evaluation).
  • 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)).
  • expression libraries containing clones by means of expression vectors from an expressing cDNA library consisting of the cDNA
  • Received marker sequences preferably contain inducible promoters.
  • the induction of expression can be done, for example, by means of an inducer, such as IPTG.
  • an inducer such as IPTG.
  • 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, and these can be prepared according to standard works, such as Sambrook et al., Molecular Cloning, Laboratory Handbook, 2nd edition (1989), CSH press, CoId Spring Harbor, New York Further preferred are expression libraries which are tissue-specific.
  • expression libraries which can be obtained by exon trapping are also included in the invention, and instead of an expression library it is possible to speak synonymously of an expression library.
  • UnicloneO library protein biochips or corresponding expression libraries which have no redundancy
  • UnicloneO library protein biochips or corresponding expression libraries which have no redundancy
  • WO 99/57311 and WO 99/57312 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 containing, for example, at least one affinity epitope or "tag".
  • 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 domain, green fluorescent protein, maltose binding protein, calmodulin binding protein, glutathione S-transferase or lacZ.
  • a marker sequence can also be composed of several individual marker sequences. This may involve cloning individual fragments into a large common fragment and expressing this combined fragment.
  • solid support includes embodiments such as a filter, a membrane, a magnetic or fluorophore-labeled bead, a 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 size 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
  • Characterizing a substance for multiple sclerosis characterized in that an arrangement or assay according to the invention is brought into contact with a.) At least one substance to be investigated and b.) A binding success is detected.
  • the invention relates to a method for identifying and characterizing a substance for multiple sclerosis, characterized in that an 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 assayed may be any native or non-native biomolecule, synthetic chemical molecule, mixture or substance library.
  • the evaluation of the binding success is carried out, for example, using commercially available image analysis software (GenePix Pro (Axon Laboratories), Aida (Raytest), ScanArray (Packard Bioscience).
  • protein to marker sequence such as antigen / antibody
  • corresponding "means for detecting binding success" can be accomplished, for example, by
  • Fluorescent labeling, biotinization, radio-isotopic labeling or colloidal gold or latex particle marking in a conventional manner Detection of bound antibodies is accomplished using secondary antibodies labeled with commercial reporter molecules (eg, Cy, Alexa, Dyomics, FITC or similar fluorescent dyes, colloidal gold or latex particles), or with reporter enzymes such as alkaline phosphatase, horseradish peroxidase, etc. and the corresponding colorimetric, fluorescent or chemiluminescent substrates.
  • reporter molecules eg, Cy, Alexa, Dyomics, FITC or similar fluorescent dyes, colloidal gold or latex particles
  • reporter enzymes such as alkaline phosphatase, horseradish peroxidase, etc. and the corresponding colorimetric, fluorescent or chemiluminescent substrates.
  • 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 for multiple sclerosis developed 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 arrangement according to the invention or an assay for the screening of drugs for multiple sclerosis.
  • the invention also relates to a target for the treatment and therapy of multiple sclerosis, each selected from the group SEQ 1 - 395 or in each case a protein coding therefor.
  • the invention also relates to the use of the marker sequences according to the invention, 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 multiple sclerosis, such as blood or plasma, bind to the marker sequences of the invention and thus the body fluid can be selectively withdrawn.
  • Ten or more patient samples were individually screened against a cDNA expression library.
  • the multiple sclerosis-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.
  • the differential clones are detected by fluorescence labeling and evaluated bioinformatorisch.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Immunology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Urology & Nephrology (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Chemical & Material Sciences (AREA)
  • Food Science & Technology (AREA)
  • Physics & Mathematics (AREA)
  • Cell Biology (AREA)
  • Rehabilitation Therapy (AREA)
  • Biotechnology (AREA)
  • Rheumatology (AREA)
  • Medicinal Chemistry (AREA)
  • Microbiology (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Peptides Or Proteins (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

L'invention concerne de nouvelles séquences de marqueurs de la sclérose en plaques et leur utilisation diagnostique ainsi qu'un procédé pour cribler des principes actifs potentiels, pouvant être utilisés contre la sclérose en plaques, au moyen de ces séquences de marqueurs. L'invention concerne en outre un dispositif diagnostique contenant de telles séquences de marqueurs de la sclérose en plaques, notamment une biopuce à protéines et son utilisation.
EP08828970A 2007-09-03 2008-09-03 Séquences de marqueurs de la sclérose en plaques et leur utilisation Ceased EP2201132A2 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP16192464.2A EP3147663A2 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation
EP16164136.0A EP3070473A2 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation
EP14164521.8A EP2884279A3 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102007041657A DE102007041657A1 (de) 2007-09-03 2007-09-03 Markersequenzen für Multiple Sklerose und deren Verwendung
PCT/DE2008/001546 WO2009030225A2 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs de la sclérose en plaques et leur utilisation

Related Child Applications (3)

Application Number Title Priority Date Filing Date
EP16192464.2A Division EP3147663A2 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation
EP16164136.0A Division EP3070473A2 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation
EP14164521.8A Division EP2884279A3 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation

Publications (1)

Publication Number Publication Date
EP2201132A2 true EP2201132A2 (fr) 2010-06-30

Family

ID=40299108

Family Applications (4)

Application Number Title Priority Date Filing Date
EP16164136.0A Withdrawn EP3070473A2 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation
EP08828970A Ceased EP2201132A2 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs de la sclérose en plaques et leur utilisation
EP16192464.2A Withdrawn EP3147663A2 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation
EP14164521.8A Withdrawn EP2884279A3 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP16164136.0A Withdrawn EP3070473A2 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation

Family Applications After (2)

Application Number Title Priority Date Filing Date
EP16192464.2A Withdrawn EP3147663A2 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation
EP14164521.8A Withdrawn EP2884279A3 (fr) 2007-09-03 2008-09-03 Séquences de marqueurs pour la sclérose multiple et leur utilisation

Country Status (7)

Country Link
US (2) US20100280224A1 (fr)
EP (4) EP3070473A2 (fr)
CN (1) CN101842495A (fr)
AU (1) AU2008295291A1 (fr)
CA (1) CA2698424A1 (fr)
DE (1) DE102007041657A1 (fr)
WO (1) WO2009030225A2 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2437060A1 (fr) * 2010-10-01 2012-04-04 Protagen AG Séquences de marqueurs pour la sclérose multiple et leur utilisation
DE102010042359A1 (de) * 2010-10-12 2012-04-12 Protagen Ag Markersequenzen für Multiple Sklerose und deren Verwendung

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EP1073771B1 (fr) 1998-04-30 2004-12-01 Max-Planck-Gesellschaft Zur Förderung Der Wissenschaften E.V. Nouveau procede permettant la selection de clones dans une banque d'expression et comprenant un rearrangement
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JP4035600B2 (ja) * 2002-05-22 2008-01-23 国立大学法人 東京大学 イマチニブに対する感受性の判定方法
EP2322201A3 (fr) * 2002-10-29 2011-07-27 Genentech, Inc. Les compositions et les methodes pour le traitement de maladies liées immunisées
EP1752536A4 (fr) * 2004-05-11 2008-04-16 Alphagen Co Ltd Polynucleotide provoquant l'interference rna et procede de regulation d'expression genetique avec l'usage de ce dernier
JP2008506415A (ja) * 2004-07-19 2008-03-06 ユニバーシティー オブ ロチェスター 神経変性疾患の生物マーカー
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DE102005002110A1 (de) * 2005-01-17 2006-07-27 Protagen Ag Regulatorische-T-Zellen enthaltend Proteine zur Therapie und Diagnose von Erkrankungen
DK1929297T3 (da) * 2005-09-29 2013-03-04 Caprion Proteomics Usa Llc Biomarkører for dissemineret sklerose og fremgangsmåder til anvendelse heraf

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Also Published As

Publication number Publication date
EP3147663A2 (fr) 2017-03-29
US20100280224A1 (en) 2010-11-04
DE102007041657A1 (de) 2009-03-05
WO2009030225A3 (fr) 2009-10-01
AU2008295291A1 (en) 2009-03-12
EP3070473A2 (fr) 2016-09-21
EP2884279A2 (fr) 2015-06-17
US20150024962A1 (en) 2015-01-22
CA2698424A1 (fr) 2009-03-12
CN101842495A (zh) 2010-09-22
EP2884279A3 (fr) 2015-10-07
WO2009030225A2 (fr) 2009-03-12

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