DK2463305T3 - Antistoffer mod OX-2/CD200 og anvendelser deraf - Google Patents

Antistoffer mod OX-2/CD200 og anvendelser deraf Download PDF

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DK2463305T3
DK2463305T3 DK11005097.8T DK11005097T DK2463305T3 DK 2463305 T3 DK2463305 T3 DK 2463305T3 DK 11005097 T DK11005097 T DK 11005097T DK 2463305 T3 DK2463305 T3 DK 2463305T3
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amino acid
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Kathrine S Bowdish
Anke Kretz-Rommel
Mcknight Susan Faas
Jeremy P Springhorn
Dayang Wu
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Alexion Pharma Inc
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    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/30Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
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    • C07K2317/00Immunoglobulins specific features
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    • C07K2317/24Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
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    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation

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Claims (18)

1. Farmaceutisk sammensætning, der omfatter et farmaceutisk acceptabelt bæremiddel og en effektiv mængde af et anti-CD200-antistof, hvor anti-CD200-antistoffet: (i) hæmmer interaktionen mellem CD200 og CD200R; og (ii) omfatter en variant Fc-konstant region, som: (a) er en variant Fc-konstant region, hvor CH1- og hængselregionen stammer fra human IgG2, og CH2- og CH3-regionerne stammer fra human IgG4; (b) omfatter den ene eller begge af: (A) en phenylalanin-til- alanin-substitution i position 234 og (B) en leucin-til-alanin-substitution i position 235 ifølge EU-indekset; (c) omfatter en K322A-mutation i CH2-domænet ifølge EU-indekset; eller (d) mangler en hængselregion.
2. Farmaceutisk sammensætning ifølge krav 1, hvor anti-CD200-antistoffet er et murint antistof, et kimærisk antistof, et humaniseret antistof, et deimmuniseret antistof eller et humant antistof.
3. Farmaceutisk sammensætning ifølge krav 1, hvor anti-CD200-antistoffet omfatter: I. (a) et let kæde-polypeptid, der omfatter: (i) aminosyreresterne 21 til 127 af SEQ ID NO: 24; eller (ii) aminosyreresterne 21 til 234 af SEQ ID NO: 24; og (b) et tung kæde-polypeptid, der omfatter: (iii) aminosyreresterne 21 til 137 af SEQ ID NO: 15; eller (iv) aminosyreresterne 21 til 463 af SEQ ID NO: 15; II. (a) et let kæde-polypeptid, der omfatter: (i) aminosyreresterne 21 til 127 af SEQ ID NO: 32; eller (ii) aminosyreresterne 21 til 234 af SEQ ID NO: 32; og (b) et tung kæde-polypeptid, der omfatter: (iii) aminosyreresterne 21 til 142 af SEQ ID NO: 20; Ill . (a) et let kæde-polypeptid, der omfatter: (i) aminosyreresterne 23 til 129 af SEQ ID NO: 28; eller (ii) aminosyreresterne 23 til 236 af SEQ ID NO: 28; og (b) et tung kæde-polypeptid, der omfatter: (iii) aminosyreresterne 20 til 136 af SEQ ID NO: 13; eller (iv) aminosyreresterne 20 til 462 af SEQ ID NO: 13; eller IV. (a) et tung kæde-polypeptid, der omfatter: (i) aminosyreresterne 20 til 136 af SEQ ID NO: 11; eller (ii) aminosyreresterne 20 til 136 af SEQ ID NO: 9; og (b) et let kæde-polypeptid, der omfatter aminosyreresterne 23 til 129 af SEQ ID NO: 26.
4. Farmaceutisk sammensætning ifølge krav 1, hvor den variante Fc-konstante region har nul ADCC- eller CDC-aktivitet.
5. Farmaceutisk sammensætning ifølge et hvilket som helst af kravene 1-4 til anvendelse til behandling af cancer.
6. Farmaceutisk sammensætning til anvendelse ifølge krav 5, hvor canceren omfatter cancerceller, der udtrykker CD200.
7. Farmaceutisk sammensætning til anvendelse ifølge krav 6, hvor cancercellerne overudtrykker CD200 i forhold til normale celler af samme histologiske type som de celler, hvorfra cancercellerne er afledt.
8. Farmaceutisk sammensætning til anvendelse ifølge krav 7, hvor canceren er udvalgt fra gruppen, der består af crista neuralis-cellecancer, plasmacellecancer, lymfom, leukæmi, ovariecancer, hudcancer, lungecancer, nyrecancer, brystcancer, prostatacancer, neuroblastom og myelom.
9. Anti-CD200-antistof til anvendelse til behandling af cancer, hvor anti-CD200-antistoffet: (i) hæmmer interaktionen mellem CD200 og CD200R; og (ii) omfatter en variant Fc-konstant region, som: (a) er en variant Fc-konstant region, hvor CH1- og hængselregionen stammer fra human IgG2, og CH2- og CH3-regionerne stammer fra human IgG4; (b) omfatter den ene eller begge af: (A) en phenylalanin-til- alanin-substitution i position 234 og (B) en leucin-til-alanin-substitution i position 235 ifølge EU-indekset; (c) omfatter en K322A-mutation i CH2-domænet ifølge EU-indekset; eller (d) mangler en hængselregion.
10. Anti-CD200-antistof ifølge krav 9 til anvendelse ifølge krav 9, hvor anti-CD200-antistoffet er et murint antistof, et kimærisk antistof, et humaniseret antistof, et deimmuniseret antistof eller et humant antistof.
11. Anti-CD200-antistof ifølge krav 9 til anvendelse ifølge krav 9, hvor anti-CD200-antistoffet omfatter: I. (a) et let kæde-polypeptid, der omfatter: (i) aminosyreresterne 21 til 127 af SEQ ID NO: 24; eller (ii) aminosyreresterne 21 til 234 af SEQ ID NO: 24; og (b) et tung kæde-polypeptid, der omfatter: (iii) aminosyreresterne 21 til 137 af SEQ ID NO: 15; eller (iv) aminosyreresterne 21 til 463 af SEQ ID NO: 15; II. (a) et let kæde-polypeptid, der omfatter: (i) aminosyreresterne 21 til 127 af SEQ ID NO: 32; eller (ii) aminosyreresterne 21 til 234 af SEQ ID NO: 32; og (b) et tung kæde-polypeptid, der omfatter: (iii) aminosyreresterne 21 til 142 af SEQ ID NO: 20; III. (a) et let kæde-polypeptid, der omfatter: (i) aminosyreresterne 23 til 129 af SEQ ID NO: 28; eller (ii) aminosyreresterne 23 til 236 af SEQ ID NO: 28; og (b) et tung kæde-polypeptid, der omfatter: (iii) aminosyreresterne 20 til 136 af SEQ ID NO: 13; eller (iv) aminosyreresterne 20 til 462 af SEQ ID NO: 13; eller IV. (a) et tung kæde-polypeptid, der omfatter: (i) aminosyreresterne 20 til 136 af SEQ I D NO: 11; eller (ii) aminosyreresterne 20 til 136 af SEQ ID NO: 9; og (b) et let kæde-polypeptid, der omfatter aminosyreresterne 23 til 129 af SEQ ID NO: 26.
12. Anti-CD200-antistof ifølge krav 9 til anvendelse ifølge krav 9, hvor den variante Fc-konstante region har nul ADCC-eller CDC-aktivitet.
13. Anti-CD200-antistof ifølge et hvilket som helst af kravene 9-12 til anvendelse ifølge et hvilket som helst af kravene 9-12, hvor canceren omfatter cancerceller, der udtrykker CD200.
14. Anti-CD200-antistof ifølge krav 13 til anvendelse ifølge krav 13, hvor cancercellerne overudtrykker CD200 i forhold til normale celler af samme histologiske type som de celler, hvorfra cancercellerne er afledt.
15. Anti-CD200-antistof ifølge et hvilket som helst af kravene 9-14 til anvendelse ifølge et hvilket som helst af kravene 9-14, hvor canceren er udvalgt fra gruppen, der består af crista neuralis-cellecancer, plasmacellecancer, lymfom, leukæmi, ovariecancer, hudcancer, lungecancer, nyrecancer, brystcancer, prostatacancer, neuroblastom og myelom.
16. Anti-CD200-antistof ifølge et hvilket som helst af kravene 9-15 til anvendelse ifølge et hvilket som helst af kravene 9-15, hvor patienten skal have administreret et andet middel eller en terapi.
17. Anti-CD200-antistof ifølge krav 16 til anvendelse ifølge krav 16, hvor det andet middel er et kemoterapeutisk middel.
18. Anti-CD200-antistof ifølge krav 16 til anvendelse ifølge krav 16, hvor terapien er strålebehandling.
DK11005097.8T 2006-01-12 2007-01-11 Antistoffer mod OX-2/CD200 og anvendelser deraf DK2463305T3 (da)

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US75842606P 2006-01-12 2006-01-12
US75908506P 2006-01-12 2006-01-12
US80199106P 2006-05-18 2006-05-18
EP07716538A EP1984403A2 (en) 2006-01-12 2007-01-11 Antibodies to ox-2/cd200 and uses thereof

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US (3) US8075884B2 (da)
EP (3) EP3101033B1 (da)
JP (3) JP5404052B2 (da)
KR (2) KR20140091765A (da)
CN (1) CN103690947A (da)
AU (1) AU2007207764B2 (da)
BR (1) BRPI0707126A2 (da)
CA (1) CA2636577C (da)
DK (1) DK2463305T3 (da)
ES (2) ES2586825T3 (da)
HU (1) HUE028179T2 (da)
IL (1) IL192668A (da)
MX (1) MX2008009015A (da)
NZ (2) NZ599035A (da)
PL (1) PL2463305T3 (da)
PT (1) PT2463305T (da)
RU (2) RU2520088C2 (da)
SG (2) SG10201400426XA (da)
SI (1) SI2463305T1 (da)
TW (1) TW200804422A (da)
WO (1) WO2007084321A2 (da)

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