DK2484696T3 - Antagonistiske hLIGHT-specifikke humane monoklonale antistoffer - Google Patents

Antagonistiske hLIGHT-specifikke humane monoklonale antistoffer Download PDF

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DK2484696T3
DK2484696T3 DK12162958.8T DK12162958T DK2484696T3 DK 2484696 T3 DK2484696 T3 DK 2484696T3 DK 12162958 T DK12162958 T DK 12162958T DK 2484696 T3 DK2484696 T3 DK 2484696T3
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hlight
pta
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nos
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Steven W Granger
Shinichiro Kato
Carl F Ware
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Kyowa Hakko Kirin Co Ltd
Lajolla Inst For Allergy And Immunology
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    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • 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
    • AHUMAN NECESSITIES
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    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
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    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
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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
    • C07K16/2875Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the NGF/TNF superfamily, e.g. CD70, CD95L, CD153, CD154
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    • C12N15/09Recombinant DNA-technology
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/565Complementarity determining region [CDR]
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    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76Antagonist effect on antigen, e.g. neutralization or inhibition of binding

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Claims (21)

1. Isoleret antistof eller et hLIGHT-bindingsfragment deraf, hvor antistoffet og fragmentet deraf binder sig til den trimere men ikke til den monomere form af hLIGHT, hvor binding til hLIGHT-epitopen fra antistoffets og fragmentets side blokeres kompetitivt af et antistof dannet af hybridomet med ATCC-tilgangsnummer PTA-7819, og hvor bindingen ikke blokeres kompetitivt af antistofferne dannet af hybridomerne med ATCC-tilgangsnumrene PTA-7729, PTA-7842 og PTA-7818, hvor antistoffet og fragmentet hæmmer binding af HVEM og LTpR til hLIGHT, og hvor antistoffet og fragmentet binder sig til enkeltnukleotidpolymor-fisme(SNP)hLIGHT-varianterne 214E-32S og 214K-32S, 214E-32L og 214K-32L, hvor antistoffet er et antagonistantistof.
2. Antistof eller hLIGHT-bindingsfragment deraf ifølge krav 1, hvor binding til hLIGHT-epitopen fra antistoffets og fragmentets side blokeres kompetitivt af et antistof dannet af hybridomet med ATCC-tilgangsnummer PTA-7728.
3. Antistof eller hLIGHT-bindingsfragment deraf ifølge krav 1 eller krav 2, hvor antistoffet konkurrerer med HVEM, LTPR eller et fusionsprotein deraf om binding til celleoverfla-deudtrykt hLIGHT eller opløselig hLIGHT.
4. Antistof eller hLIGHT-bindingsfragment deraf ifølge et hvilket som helst af kravene 1 til 3, hvor antistoffet omfatter: et VH-domæne med aminosyresekvensen fra rest 27 til rest 143 i SEQ ID NO: 5 og et VL-domæne med aminosyresekvensen fra rest 23 til rest 129 i SEQ ID NO: 10.
5. Antistof eller hLIGHT-bindingsfragment deraf ifølge et hvilket som helst af kravene 1 til 3, hvor antistoffet omfatter: (a) en variabel tungkæderegion omfattende VH CDR1 med aminosyresekvensen ifølge SEQ ID NO:23, en VH CDR2 med aminosyresekvensen ifølge SEQ ID NO:24 og en VH CDR3 med aminosyresekvensen ifølge SEQ ID NO:25; og (b) en variabel letkæderegion omfattende VL CDR1 med aminosyresekvensen ifølge SEQ ID NO:38, en VL CDR2 med aminosyresekvensen ifølge SEQ ID NO:39 og en VL CDR3 med aminosyresekvensen ifølge SEQ ID NO:40.
6. Antistof eller hLIGHT-bindingsfragment deraf ifølge et hvilket som helst af kravene 1 til 3, hvor antistoffet omfatter en VH og en VL af et antistof dannet af et hybridom med ATCC-tilgangsnummer PTA-7728.
7. Antistof eller hLIGHT-bindingsfragment deraf ifølge et hvilket som helst af kravene 1 til 3, hvor antistoffet omfatter (a) en VH CDR1, VH CDR2 og VH CDR3 og (b) en VL CDR1, VL CDR2 og VL CDR3 af et antistof dannet af et hybridom med ATCC-tilgangsnummer PTA-7728.
8. Antistof eller hLIGHT-bindingsfragment deraf ifølge krav 1, hvor antistoffet dannes af et hybridom med ATCC-tilgangsnummer PTA-7728.
9. Antistof eller hLIGHT-bindingsfragment deraf ifølge et hvilket som helst af kravene 1 til 8, hvor antistoffet er et fuldstændigt humant antistof, et kimært antistof eller et humaniseret antistof.
10. Antistof eller hLIGHT-bindingsfragment deraf ifølge et hvilket som helst af kravene 1 til 9, hvor antistoffet er et monoklonalt antistof.
11. Antistof eller hLIGHT-bindingsfragment deraf ifølge et hvilket som helst af kravene 1 til 10, hvor antistoffet er et rekombinant antistof.
12. hLIGHT-bindingsfragmentet ifølge et hvilket som helst af kravene 1 til 11, hvor fragmentet er et Fab-fragment, F(ab')2-fragment, enkeltkæde-Fv (scFv), diaantistof, triaan-tistof eller miniantistof.
13. Sammensætning omfattende antistoffet eller hLIGHT-bindingsfragmentet deraf ifølge et hvilket som helst af kravene 1 til 12.
14. Isoleret nukleinsyremolekyle kodende for antistoffet eller hLIGHT-bindingsfragmentet deraf ifølge et hvilket som helst af kravene 1 til 12.
15. Vektor, som omfatter nukleinsyremolekylet ifølge krav 14.
16. Værtscelle, som omfatter vektoren ifølge krav 15.
17. Fremgangsmåde til frembringelse af antistoffet eller hLIGHT-bindingsfragmentet deraf ifølge et hvilket som helst af kravene 1-12, hvilken fremgangsmåde omfatter; at dyrke værtscellen ifølge krav 16, at udtrykke antistoffet eller hLIGHT-bindingsfragmentet deraf, og at indvinde antistoffet eller hLIGHT-bindingsfragmentet deraf.
18. Hybridom, der danner antistoffet ifølge et hvilket som helst af kravene 1 til 8.
19. Hybridom ifølge krav 18, som danner antistoffet ifølge et hvilket som helst af kravene 1 eller 3 til 12, hvor hybridomet har ATCC-tilgangsnummeret PTA-7728 (124 F23).
20. Farmaceutisk sammensætning indeholdende antistoffet eller hLIGHT-bindingsfragmentet deraf ifølge et hvilket som helst af kravene 1 til 12 i et farmaceutisk acceptabelt bærestof.
21. Sæt, som omfatter antistoffet eller hLIGHT-bindingsfragmentet deraf ifølge et hvilket som helst af kravene 1 til 12, eller et sæt, som omfatter sammensætningen ifølge krav 13.
DK12162958.8T 2006-08-28 2007-08-24 Antagonistiske hLIGHT-specifikke humane monoklonale antistoffer DK2484696T3 (da)

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US84077406P 2006-08-28 2006-08-28
US89787507P 2007-01-25 2007-01-25
EP10172151.2A EP2292663B1 (en) 2006-08-28 2007-08-24 Antagonistic human light-specific human monoclonal antibodies

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