JP2015501149A5 - - Google Patents

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JP2015501149A5
JP2015501149A5 JP2014535903A JP2014535903A JP2015501149A5 JP 2015501149 A5 JP2015501149 A5 JP 2015501149A5 JP 2014535903 A JP2014535903 A JP 2014535903A JP 2014535903 A JP2014535903 A JP 2014535903A JP 2015501149 A5 JP2015501149 A5 JP 2015501149A5
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  1. 列番号8のVH配列及び配列番号7のVL配列を含む抗体と競合的にHtrA1に結合する、単離された抗体
  2. 競合的結合がELISAアッセイを用いて決定される、請求項1に記載の抗体。
  3. HtrA1に結合する単離された抗体であって、該抗体は、(i)HtrA1のN224、K248、又は両方を含むエピトープに結合し、(ii)IC50≦30nMでHtrA1を阻害する抗体。
  4. 抗体は次の特性:(i)HtrA1三量体の1つのサブユニットに対して1つの可変ドメインの比率でHtrA1に結合すること、又は(ii)HtrA1の三量体形成を妨げないこと一又は複数を更に含む、請求項3に記載の抗体。
  5. IC50が配列番号12を有する基質によるセリンプロテアーゼアッセイを用いて決定される、請求項3に記載の抗体。
  6. 抗体は、HtrA2、HtrA3及びHtrA4の一又は複数と交差反応しない、請求項1から5の何れか一項に記載の抗体。
  7. 抗体は、≦500nMの解離定数を有する、請求項1から6の何れか一項に記載の抗体。
  8. 解離定数がFabを使用したビアコアにより25℃で決定される、請求項6に記載の抗体。
  9. モノクローナル、ヒト、ヒト化、又はキメラ抗体、又は、HtrA1に結合する抗体断片である、請求項1から8の何れか一項に記載の抗体。
  10. 抗体は、(a)アミノ酸配列GTFLTXWGHYFDYを含むHVR−H3(ここでXはS又はTである(配列番号27));(b)アミノ酸配列QQXPXTを含むHVR−L3(ここでXはS、V又はDであり;XはY、D又はSであり;XはT、S、A、D又はNであり;XはT、H、N、S、A、L又はRであり;及びXはP、T、A又はSである(配列番号24));及び(c)アミノ酸配列WIDPYGGDTXYADSVKGを含むHVR−H2(ここでXはN又はDである(配列番号26)を含む、請求項1からの何れか一項に記載の抗体。
  11. 抗体は、(a)配列番号6のアミノ酸配列を含むHVR−H3、(b)配列番号3のアミノ酸配列を含むHVR−L3、及び(c)配列番号5のアミノ酸配列を含むHVR−H2を含む、請求項1から10の何れか一項に記載の抗体。
  12. 抗体は、(a)配列番号6のアミノ酸配列を含むHVR−H3、(b)配列番号19のアミノ酸配列を含むHVR−L3、及び(c)配列番号5のアミノ酸配列を含むHVR−H2を含む、請求項1から11の何れか一項に記載の抗体。
  13. 抗体は、(a)配列番号6のアミノ酸配列を含むHVR−H3、(b)配列番号22のアミノ酸配列を含むHVR−L3、及び(c)配列番号5のアミノ酸配列を含むHVR−H2を含む、請求項1から10の何れか一項に記載の抗体。
  14. 抗体は、(a)アミノ酸配列GFXIXYYIHを含むHVR−H1(ここでXはN、S又はTであり;XはS、D、Y又はAであり;及びXはG又はDである(配列番号25));(b)アミノ酸配列WIDPYGGDTXYADSVKGを含むHVR−H2(ここでXはN又はDである(配列番号26));及び(c)アミノ酸配列GTFLTXWGHYFDYを含むHVR−H3(ここでXはS又はTである(配列番号27))を含む、請求項1から10の何れか一項に記載の抗体。
  15. 抗体は、(a)アミノ酸配列RASQXAを含むHVR−L1(ここでXはD、S又はVであり;XはV又はIであり;XはS、N又はGであり;XはT又はNであり;XはA又はYであり;及びXはV又はLである(配列番号23));(b)配列番号2のアミノ酸配列を含むHVR−L2;及び(c)アミノ酸配列QQXPXTを含むHVR−L3(ここでXはS、V又はDであり;XはY、D又はSであり;XはT、S、A、D又はNであり;XはT、H、N、S、A、L又はRであり;及びXはP、T、A又はSである(配列番号24))を更に含む、請求項1から10及び14の何れか一項に記載の抗体。
  16. 抗体は、
    (a)配列番号4のアミノ酸配列を含むHVR−H1;(b)配列番号5のアミノ酸配列を含むHVR−H2;及び(c)配列番号6のアミノ酸配列を含むHVR−H3;
    (a)配列番号20のアミノ酸配列を含むHVR−H1;(b)配列番号5のアミノ酸配列を含むHVR−H2;及び(c)配列番号6のアミノ酸配列を含むHVR−H3;
    (a)配列番号1のアミノ酸配列を含むHVR−L1;(b)配列番号2のアミノ酸配列を含むHVR−L2;及び(c)配列番号3のアミノ酸配列を含むHVR−H3;
    (a)配列番号18のアミノ酸配列を含むHVR−L1;(b)配列番号2のアミノ酸配列を含むHVR−L2;及び(c)配列番号19のアミノ酸配列を含むHVR−L3;又は
    (a)配列番号21のアミノ酸配列を含むHVR−L1;(b)配列番号2のアミノ酸配列を含むHVR−L2;及び(c)配列番号22のアミノ酸配列を含むHVR−L3
    を含む、請求項1から10、14及び15の何れか一項に記載の抗体。
  17. 抗体は、
    (a)配列番号1のアミノ酸配列を含むHVR−L1;(b)配列番号2のアミノ酸配列を含むHVR−L2;及び(c)配列番号3のアミノ酸配列を含むHVR−L3;
    (a)配列番号18のアミノ酸配列を含むHVR−L1;(b)配列番号2のアミノ酸配列を含むHVR−L2;及び(c)配列番号19のアミノ酸配列を含むHVR−L3;又は
    (a)配列番号21のアミノ酸配列を含むHVR−L1;(b)配列番号2のアミノ酸配列を含むHVR−L2;及び(c)配列番号22のアミノ酸配列を含むHVR−L3
    を更に含む、請求項16に記載の抗体。
  18. 配列番号17の重鎖可変ドメインのフレームワーク(FR2)配列を更に含む、請求項1から17の何れか一項に記載の抗体。
  19. (a)配列番号8のアミノ酸配列に少なくとも95%の配列同一性を有するVH配列;(b)配列番号7のアミノ酸配列に少なくとも95%の配列同一性を有するVL配列;又は(c)(a)のVH配列及び(b)のVL配列を含む、請求項1から18の何れか一項に記載の抗体。
  20. (a)配列番号32を含むVH配列;(b)配列番号31を含むVL配列;又は(c)配列番号32を含むVH配列及び配列番号31を含むVL配列を含む、請求項1から19の何れか一項に記載の抗体。
  21. 配列番号8のVH配列;配列番号7のVL配列;配列番号30のVL配列;配列番号28のVL配列;又は配列番号29のVH配列を含む、請求項19又は20に記載の抗体。
  22. 配列番号8のVH配列及び配列番号7のVL配列;配列番号29のVH配列及び配列番号28のVL配列;又は配列番号30のVL配列及び配列番号29のVH配列を含む抗体。
  23. (a)配列番号8のアミノ酸配列に少なくとも95%の配列同一性を有するVH配列;(b)配列番号7のアミノ酸配列に少なくとも95%の配列同一性を有するVL配列;又は(c)(a)のVH配列及び(b)のVL配列を含む、HtrA1に結合する抗体。
  24. (a)配列番号32を含むVH配列;(b)配列番号31を含むVL配列;又は(c)配列番号32を含むVH配列及び配列番号31を含むVL配列を含む、HtrA1に結合する抗体。
  25. (a)アミノ酸配列GFXIXYYIHを含むHVR−H1(ここでXはN、S又はTであり;XはS、D、Y又はAであり;及びXはG又はDである(配列番号25));(b)アミノ酸配列WIDPYGGDTXYADSVKGを含むHVR−H2(ここでXはN又はDである(配列番号26));c)アミノ酸配列GTFLTXWGHYFDYを含むHVR−H3(ここでXはS又はTである(配列番号27);(d)アミノ酸配列RASQXAを含むHVR−L1(ここでXはD、S又はVであり;XはV又はIであり;XはS、N又はGであり;XはT又はNであり;XはA又はYであり;及びXはV又はLである(配列番号23));(e)配列番号2のアミノ酸配列を含むHVR−L2;及び(f)アミノ酸配列QQXPXTを含むHVR−L3(ここでXはS、V又はDであり;XはY、D又はSであり;XはT、S、A、D又はNであり;XはT、H、N、S、A、L又はRであり;及びXはP、T、A又はSである(配列番号24))を含む抗体。
  26. 抗体は、(a)配列番号4、20、及び47−51から選択されるアミノ酸配列を含むHVR−H1;(b)配列番号5及び52から選択されるアミノ酸配列を含むHVR−H2;(c)配列番号6及び53から選択されるアミノ酸配列を含むHVR−H3;(d)配列番号1、18、21及び33から選択されるアミノ酸配列を含むHVR−L1;(e)配列番号2のアミノ酸配列を含むHVR−L2;及び(f)配列番号3、19、22及び34−46から選択されるアミノ酸配列を含むHVR−L3を含む、請求項25に記載の抗体。
  27. 抗体は、
    (a)配列番号4のアミノ酸配列を含むHVR−H1;(b)配列番号5のアミノ酸配列を含むHVR−H2;(c)配列番号6のアミノ酸配列を含むHVR−H3;(d)配列番号1のアミノ酸配列を含むHVR−L1;(e)配列番号2のアミノ酸配列を含むHVR−L2;及び(f)配列番号3のアミノ酸配列を含むHVR−L3
    (a)配列番号20のアミノ酸配列を含むHVR−H1;(b)配列番号5のアミノ酸配列を含むHVR−H2;(c)配列番号6のアミノ酸配列を含むHVR−H3;(d)配列番号18のアミノ酸配列を含むHVR−L1;(e)配列番号2のアミノ酸配列を含むHVR−L2;及び(f)配列番号19のアミノ酸配列を含むHVR−L3;又は
    (a)配列番号20のアミノ酸配列を含むHVR−H1;(b)配列番号5のアミノ酸配列を含むHVR−H2;(c)配列番号6のアミノ酸配列を含むHVR−H3;(d)配列番号21のアミノ酸配列を含むHVR−L1;(e)配列番号2のアミノ酸配列を含むHVR−L2;及び(f)配列番号22のアミノ酸配列を含むHVR−L3
    を含む、請求項26に記載の抗体。
  28. (a)配列番号87のアミノ酸配列を含むHVR−H1;(b)配列番号88のアミノ酸配列を含むHVR−H2;及び(c)配列番号89のアミノ酸配列を含むHVR−H3を含む、請求項1から9の何れか一項に記載の抗体。
  29. (a)配列番号85のアミノ酸配列を含むHVR−L1;(b)配列番号58のアミノ酸配列を含むHVR−L2;及び(c)配列番号86のアミノ酸配列を含むHVR−L3を更に含む、請求項1から9及び28の何れか一項に記載の抗体。
  30. (a)配列番号87のアミノ酸配列を含むHVR−H1;(b)配列番号88のアミノ酸配列を含むHVR−H2;(c)配列番号89のアミノ酸配列を含むHVR−H3;(d)配列番号85のアミノ酸配列を含むHVR−L1;(e)配列番号58のアミノ酸配列を含むHVR−L2;及び(f)配列番号86のアミノ酸配列を含むHVR−L3を含む、抗体。
  31. (a)配列番号25のアミノ酸配列を含むHVR−H1;(b)配列番号26のアミノ酸配列を含むHVR−H2;(c)配列番号27のアミノ酸配列を含むHVR−H3;(d)配列番号23のアミノ酸配列を含むHVR−L1;(e)配列番号2のアミノ酸配列を含むHVR−L2;及び(f)配列番号24のアミノ酸配列を含むHVR−L3を含む、請求項30に記載の抗体。
  32. (a)配列番号4、20、47〜51、及び75〜80から選択されるアミノ酸配列を含むHVR−H1;(b)配列番号5、52、及び81〜82から選択されるアミノ酸配列を含むHVR−H2;(c)配列番号6、53、83〜84から選択されるアミノ酸配列を含むHVR−H3;(d)配列番号1、18、21、33、及び54〜57から選択されるアミノ酸配列を含むHVR−L1;(e)配列番号2、及び58から選択されるアミノ酸配列を含むHVR−L2;及び(f)配列番号3、19、22、34〜46、及び59〜74から選択されるアミノ酸配列を含むHVR−L3を含む、請求項30又は31に記載の抗体。
  33. HtrA1に結合し、かつ、1以上のHtrA1基質に対するそのセリンプロテアーゼ活性を阻害する、単離された抗体。
  34. 50nM未満のIC 50 でHtrA1を阻害する、請求項33に記載の抗体。
  35. 完全長IgG1又はIgG4抗体である、請求項1から34の何れか一項に記載の抗体。
  36. 請求項1から35の何れか一項に記載の抗体をコードする単離された核酸。
  37. 請求項36に記載の核酸を含む宿主細胞。
  38. 抗HtrA1抗体をコードする核酸の発現に適した条件下で、請求項37に記載の宿主細胞を培養することを含む、抗体を産生する方法。
  39. 宿主細胞から抗HtrA1抗体を回収することを更に含む、請求項38に記載の方法。
  40. 請求項1から35の何れか一項に記載の抗体及び細胞傷害性薬物を含むイムノコンジュゲート。
  41. 請求項1から35の何れか一項に記載の抗体及び薬学的に許容される担体を含む薬学的製剤。
  42. 加齢性黄斑変性、地図状萎縮、糖尿病性網膜症、未熟児網膜症、又はポリープ状脈絡膜血管症を治療するための;網膜細胞又は光受容細胞の変性を阻害するための;又は眼においてHtrA1のプロテーアーゼ活性を阻害するための医薬として使用のための、請求項1から35の何れか一項に記載の抗体。
  43. 乾燥型加齢黄斑変性の治療に使用のための、請求項42に記載の抗体。
  44. 加齢性黄斑変性、地図状萎縮、糖尿病性網膜症、未熟児網膜症、又はポリープ状脈絡膜血管症を治療するための;網膜細胞又は光受容細胞の変性を阻害するための;又は眼においてHtrA1のプロテーアーゼ活性を阻害するための医薬の製造における、請求項1から35の何れか一項に記載の抗体の使用。
  45. 加齢黄斑変性が乾燥型加齢黄斑変性である、請求項44の使用。
JP2014535903A 2011-10-14 2012-10-12 抗HtrA1抗体及び使用方法 Expired - Fee Related JP6532678B2 (ja)

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