DK2383295T3 - Ip-10-antistoffer og anvendelser heraf - Google Patents
Ip-10-antistoffer og anvendelser heraf Download PDFInfo
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- DK2383295T3 DK2383295T3 DK11166104.7T DK11166104T DK2383295T3 DK 2383295 T3 DK2383295 T3 DK 2383295T3 DK 11166104 T DK11166104 T DK 11166104T DK 2383295 T3 DK2383295 T3 DK 2383295T3
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- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/24—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
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- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/52—Cytokines; Lymphokines; Interferons
- C07K14/521—Chemokines
- C07K14/522—Alpha-chemokines, e.g. NAP-2, ENA-78, GRO-alpha/MGSA/NAP-3, GRO-beta/MIP-2alpha, GRO-gamma/MIP-2beta, IP-10, GCP-2, MIG, PBSF, PF-4, KC
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
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- A—HUMAN NECESSITIES
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- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
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- C07K—PEPTIDES
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- C07K2317/33—Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
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- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
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- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/565—Complementarity determining region [CDR]
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- C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
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Claims (15)
- IP-10-ANTISTOFFER OG ANVENDEFSER HERAF1. Isoleret humant monoklonalt antistof, eller en antigenbindende del deraf, hvor antistoffet specifikt binder til human IP-10 og ikke krydsreagerer med human MIG og ikke krydsreagerer med human ITAC.
- 2. Antistof ifølge krav 1, der er et fuldlængdeantistof af en IgGl- eller IgG4-isotype eller er et antistoffragment.
- 3. Antistof eller antigen-bindende del ifølge krav 1, omfattende en tungkæde variabel region, der omfatter CDR1-, CDR2- og CDR3-sekvenser og en letkædevariabel region, der omfatter CDR1-, CDR2- og CDR3-sekvenser, hvor: (a) tungkædevariabel region CDR3-sekvensen omfatter aminosyresekvensen af SEQ ID NO: 32, og tungkædevariabel region CDR3-sekvensen omfatter aminosyresekvensen af SEQ ID NO: 81; (b) tungkædevariabel region CDR3-sekvensen omfatter aminosyresekvenserne af SEQ ID NO: 24 og tungkædevariabel region CDR3-sekvensen omfatter aminosyresekvensen af SEQ ID NO: 73 eller (c) tungkædevariabel region CDR3-sekvensen omfatter aminosyresekvenserne af SEQ ID NO: 28 og tungkædevariabel region CDR3-sekvensen omfatter aminosyresekvensen af SEQ ID NO: 77.
- 4. Antistof eller antigenbindende del ifølge et hvilket som helst af kravene 1 til 3, omfattende: (a) en tungkædevariabel region CDR1 omfattende SEQ ID NO: 9, en tungkædevariabel region CDR2 omfattende SEQ ID NO: 21, en tungkædevariabel region CDR3 omfattende SEQ ID NO: 32, en letkædevariabel region CDR1 omfattende SEQ ID NO: 59, en letkædevariabel region CDR2 omfattende SEQ ID NO: 70 og en letkædevariabel region CDR3 omfattende SEQ ID NO: 81; (b) en tungkædevariabel region CDR1 omfattende SEQ ID NO: 1, en tungkædevariabel region CDR2 omfattende SEQ ID NO: 13, en tungkædevariabel region CDR3 omfattende SEQ ID NO: 24, en letkædevariabel region CDR1 omfattende SEQ ID NO: 51, en letkædevariabel region CDR2 omfattende SEQ ID NO: 62 og en letkædevariabel region CDR3 omfattende SEQ ID NO: 73; eller (c) en tungkædevariabel region CDR1 omfattende SEQ ID NO: 5, en tungkædevariabel region CDR2 omfattende SEQ ID NO: 17, en tungkædevariabel region CDR3 omfattende SEQ ID NO: 28, en letkædevariabel region CDR1 omfattende SEQ ID NO: 55, en letkædevariabel region CDR2 omfattende SEQ ID NO: 66 og en letkædevariabel region CDR3 omfattende SEQ ID NO: 77.
- 5. Antistof eller antigen-bindende del ifølge krav 1 eller 2, der konkurrerer om binding til IP-10 med antistoffet ifølge krav 4 eller der binder til samme epitop på IP-10 som antistof ifølge krav 4.
- 6. Immunokonjugat omfattende antistoffet eller den antigenbindende del ifølge et hvilket som helst af kravene 1 til 4 bundet til et terapeutisk middel såsom et cytotoxin eller en radioaktiv isotop.
- 7. Bispecifikt molekyle omfattende antistoffet eller den antigen-bindende del ifølge et hvilket som helst af kravene 1 til 4, bundet til en anden funktionsdel med en anden bindingsspecificitet end antistoffet eller den antigenbindende del.
- 8. Sammensætning omfattende antistoffet eller den antigenbindende del ifølge et hvilket som helst af kravene 1 til 4, immunokonjugat ifølge krav 6 eller bispecifikt molekyle ifølge krav 7 og et farmaceutisk acceptabelt bærestof.
- 9. Isoleret nukleinsyremolekyle, der koder for antistoffet eller den antigenbindende del ifølge et hvilket som helst af kravene 1 til 4, eller en ekspressionsvektor omfattende nukleinsyren, eller en værtscelle omfattende ekspressionsvektoren.
- 10. Transgen mus omfattende humane immunoglobulin tung- og letkædetransgener, hvor musen udtrykker antistoffet ifølge et hvilket som helst af kravene 1 til 4, eller et hybridom fremstillet ud fra musen, hvor hybridomet producerer antistoffet.
- 11. Antistof eller antigenbindende del ifølge et hvilket som helst af kravene 1 til 4 til anvendelse i en fremgangsmåde til behandling af en inflammatorisk eller autoimmun sygdom.
- 12. Antistof eller antigenbindende del ifølge krav 11 til anvendelse i en fremgangsmåde til behandling ifølge krav 11, hvor sygdommen er udvalgt fra multipel sklerose, rheumatoid arthritis, inflammatorisk tarmsygdom (f.eks. ulcerativ colitis, Crohns sygdom), systemic lupus erythematosus, Type I diabetes, inflammatorisk hudsygdomme (f.eks. psoriasis, lichen pianus), autoimmun thyroidea-sygdom (f.eks. Graves' sygdom, Hashimotos thyroiditis), Sjogrens syndrom, lungeinflammation (f.eks. astma, kronisk obstruktiv lungesygdom, lungesarcoidose, lymfocytisk alveolitis), transplantatafstødning, rygmarvsskade, hjerneskade f.eks. apopleksi), neurodegenerative sygdomme f.eks. Alzheimers sygdom, Parkinsons sygdom), gingivitis, genterapiinduceret inflammation, angiogenesesygdomme, inflammatorisk nyresygdom f.eks. IgA-nephropati, membranoproliferativ glomerulonephritis, hurtigt progredierende glomerulonephritis) og atherosklerose.
- 13. Antistof eller antigenbindende del ifølge et hvilket som helst af kravene 1 til 4 til anvendelse i en fremgangsmåde til behandling af en virus- eller bakterieinfektion, der involverer uønsket IP-10-aktivitet.
- 14. Antistof eller antigenbindende del ifølge krav 13 til anvendelse i en fremgangsmåde til behandling ifølge krav 13, hvor virusinfektionen er medieret ved humant immundefekt virus (HIV), hepatitis C virus (HCV), herpes simplex virus type I (HSV-1) eller SARS- (Severe Acute Respiratory Syndrome) virus.
- 15. Fremgangsmåde til fremstilling af antistoffet eller den antigenbindende del som defineret i krav 1 omfattende: (a) tilvejebringelse af: (i) en tungkædevariabel region-antistofsekvens omfattende en CDRl-sekvens, der er udvalgt fra SEQ ID NO: 5, 9 og 1, en CDR2-sekvens, der er udvalgt fra SEQ ID NO: 17, 21 og 13; og en CDR3-sekvens, der er udvalgt fra SEQ ID NO: 28, 32 og 24; eller (ii) en letkædevariabel region-antistofsekvens omfattende en CDRl-sekvens, der er udvalgt fra SEQ ID NO: 55, 59 og 51, en CDR2-sekvens, der er udvalgt fra SEQ ID NO: 66, 70 og 62 og en CDR3-sekvens der er udvalgt fra SEQ ID NO: 77, 81 og 73; (b) ændring af mindst én aminosyrerest i mindst én variabel region-antistofsekvens, hvilken sekvens er udvalgt fra tungkædevariabel region-antistofsekvensen og letkædevariabel region-antistofsekvensen, for at frembringe mindst én ændret antistof sekvens; og (c) ekspression af den ændrede antistofsekvens som et protein.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US52918003P | 2003-12-10 | 2003-12-10 | |
| EP04813771A EP1691837B1 (en) | 2003-12-10 | 2004-12-10 | Ip-10 antibodies and their uses |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DK2383295T3 true DK2383295T3 (da) | 2015-06-15 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK11166104.7T DK2383295T3 (da) | 2003-12-10 | 2004-12-10 | Ip-10-antistoffer og anvendelser heraf |
| DK04813771.5T DK1691837T3 (da) | 2003-12-10 | 2004-12-10 | IP-10-antistoffer og anvendelse heraf |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK04813771.5T DK1691837T3 (da) | 2003-12-10 | 2004-12-10 | IP-10-antistoffer og anvendelse heraf |
Country Status (25)
| Country | Link |
|---|---|
| US (4) | US20050191293A1 (da) |
| EP (3) | EP2865687A1 (da) |
| JP (2) | JP4942487B2 (da) |
| KR (4) | KR20060135690A (da) |
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