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JP2018521638A5
JP2018521638A5 JP2017561965A JP2017561965A JP2018521638A5 JP 2018521638 A5 JP2018521638 A5 JP 2018521638A5 JP 2017561965 A JP2017561965 A JP 2017561965A JP 2017561965 A JP2017561965 A JP 2017561965A JP 2018521638 A5 JP2018521638 A5 JP 2018521638A5
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Claims (15)

  1. 相補性決定領域CDRH1、CDRH2およびCDRH3を含む重鎖可変領域と、相補性決定領域CDRL1、CDRL2およびCDRL3を含む軽鎖可変領域とを含む、ヒトCTLA−4タンパク質に特異的に結合する単離された抗体であって、
    (a)CDRH1が、SYXMX(配列番号22)(式中、XはSまたはAであり;XはNまたはSである)のアミノ酸配列を含む;
    (b)CDRH2が、SISSSSSYIYYADSVKG(配列番号2)のアミノ酸配列を含む;
    (c)CDRH3が、VGLMGPFXI(配列番号23)(式中、XはDまたはNである)のアミノ酸配列を含む;
    (d)CDRL1が、RASQSVXYLX(配列番号24)(式中、XはSまたはGであり;XはR、S、またはTであり;XはGまたはAである)のアミノ酸配列を含む;
    (e)CDRL2が、XSXRAT(配列番号25)(式中、XはGまたはAであり;XはAまたはTであり;XはT、S、R、またはNである)のアミノ酸配列を含む;ならびに
    (f)CDRL3が、QQYGXSPXT(配列番号26)(式中、XはSまたはTであり、XはWまたはFである)のアミノ酸配列を含む、
    前記抗体。
  2. (a)CDRH1は、配列番号1および配列番号27からなる群から選択されるアミノ酸配列を含む
    (b)CDRH3は、配列番号3および配列番号28からなる群から選択されるアミノ酸配列を含む;
    (c)CDRL1は、配列番号4、配列番号29および配列番号30からなる群から選択されるアミノ酸配列を含む;
    (d)CDRL2は、配列番号5、および配列番号31〜35からなる群から選択されるアミノ酸配列を含む;
    (e)CDRL3は、配列番号6、配列番号36および配列番号37からなる群から選択されるアミノ酸配列を含む;
    (f)CDRH1、CDRH2およびCDRH3は、それぞれ、配列番号1、配列番号2および配列番号3;配列番号27、配列番号2および配列番号3;もしくは配列番号27、配列番号2および配列番号28に記載のCDRH1、CDRH2およびCDRH3アミノ酸配列を含む;ならびに/または
    (g)CDRL1、CDRL2およびCDRL3は、それぞれ、配列番号4、配列番号5および配列番号6;配列番号29、配列番号32および配列番号36;配列番号29、配列番号33および配列番号37;配列番号30、配列番号31および配列番号6;配列番号29、配列番号34および配列番号6;または配列番号29、配列番号35および配列番号37に記載のCDRL1、CDRL2およびCDRL3アミノ酸配列を含む、
    請求項1に記載の単離された抗体。
  3. CDRH1、CDRH2、CDRH3、CDRL1、CDRL2およびCDRL3が、それぞれ、配列番号1、配列番号2、配列番号3、配列番号4、配列番号5、および配列番号6;配列番号1、配列番号2、配列番号3、配列番号29、配列番号32、および配列番号36;配列番号1、配列番号2、配列番号3、配列番号29、配列番号33、および配列番号37;配列番号27、配列番号2、配列番号3、配列番号4、配列番号5、および配列番号6;配列番号27、配列番号2、配列番号3、配列番号29、配列番号33、および配列番号37;配列番号1、配列番号2、配列番号3、配列番号30、配列番号31、および配列番号6;配列番号1、配列番号2、配列番号3、配列番号29、配列番号34、および配列番号6;配列番号1、配列番号2、配列番号3、配列番号29、配列番号35、および配列番号37;配列番号27、配列番号2、配列番号28、配列番号4、配列番号5、および配列番号6;配列番号27、配列番号2、配列番号28、配列番号29、配列番号32、および配列番号36;配列番号27、配列番号2、配列番号28、配列番号29、配列番号33、および配列番号37;または配列番号27、配列番号2、配列番号28、配列番号29、配列番号35、および配列番号37に記載のアミノ酸配列を含む、請求項1または2に記載の単離された抗体。
  4. DRH1、CDRH2、CDRH3、CDRL1、CDRL2およびCDRL3が、それぞれ、配列番号1、配列番号2、配列番号3、配列番号4、配列番号5および配列番号6に記載のアミノ酸配列を含む、請求項1〜3のいずれか一項に記載の単離された抗体。
  5. (a)重鎖可変領域は、配列番号72のアミノ酸配列を含む重鎖可変領域を含み、軽鎖可変領域は、配列番号73のアミノ酸配列を含む;
    (b)重鎖可変領域は、配列番号7および配列番号38〜42からなる群から選択されるアミノ酸配列を含み、軽鎖可変領域は、配列番号8および配列番号43〜47からなる群から選択されるアミノ酸配列を含む;ならびに/または
    (c)重鎖可変領域および軽鎖可変領域は、それぞれ、配列番号7および配列番号8;配列番号7および配列番号44;配列番号7および配列番号45;配列番号38および配列番号8;配列番号38および配列番号45;配列番号39および配列番号43;配列番号39および配列番号45;配列番号39および配列番号46;配列番号39および配列番号47;配列番号40および配列番号43;配列番号40および配列番号8;配列番号40および配列番号44;配列番号40および配列番号45;配列番号41および配列番号8;配列番号41および配列番号44;配列番号41および配列番号45;配列番号41および配列番号47;配列番号42および配列番号43;または配列番号42および配列番号45に記載のアミノ酸配列を含む、
    請求項1〜のいずれか1項に記載の単離された抗体。
  6. 重鎖可変領域および軽鎖可変領域は、それぞれ、配列番号7および8に記載のアミノ酸配列を含む、請求項1〜5のいずれか一項に記載の単離された抗体。
  7. ヒトIgG の重鎖定常領域を含み、場合により、配列番号12、配列番号76、配列番号93または配列番号97のアミノ酸配列を含む重鎖を含む、請求項1〜6のいずれか一項に記載の単離された抗体。
  8. 配列番号12または93のアミノ酸配列を含む重鎖および配列番号13のアミノ酸配列を含む軽鎖を含む、請求項1〜7のいずれか一項に記載の単離された抗体。
  9. (a)ヒト抗体である
    (b)CTLA−4に拮抗する;および/または
    (c)ヒトCD80もしくはヒトCD86へのヒトCTLA−4タンパク質の結合を阻害する、
    請求項1〜のいずれか1項に記載の単離された抗体。
  10. 二重特異性である、請求項1〜9のいずれか一項に記載の単離された抗体。
  11. 請求項1〜10のいずれか1項に記載の抗体と、薬学的に許容される担体または賦形剤とを含む医薬組成物。
  12. 請求項1〜11のいずれか1項に記載の抗体の重鎖可変領域および/もしくは軽鎖可変領域、または重鎖および/もしくは軽鎖をコードする単離されたポリヌクレオチド。
  13. 請求項12に記載のポリヌクレオチドを含む組換え宿主細胞。
  14. ポリヌクレオチドが発現され、抗体が産生されるように、請求項13に記載の宿主細胞を培養することを含む、ヒトCTLA−4に結合する抗体を産生する方法。
  15. (a)対象における抗原に応答したT細胞活性化を増加させるための;
    (b)がんを処置するための;および/または
    (c)感染症を処置するための
    請求項1〜10のいずれか一項に記載の単離された抗体または請求項11に記載の医薬組成物
JP2017561965A 2015-05-29 2016-05-27 抗ctla−4抗体およびその使用方法 Active JP6900323B2 (ja)

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US201562190653P 2015-07-09 2015-07-09
US62/190,653 2015-07-09
US201562257202P 2015-11-18 2015-11-18
US62/257,202 2015-11-18
US201662280263P 2016-01-19 2016-01-19
US62/280,263 2016-01-19
US201662292500P 2016-02-08 2016-02-08
US62/292,500 2016-02-08
US201662294558P 2016-02-12 2016-02-12
US62/294,558 2016-02-12
US201662323226P 2016-04-15 2016-04-15
US62/323,226 2016-04-15
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