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JP2018154628A5
JP2018154628A5 JP2018088769A JP2018088769A JP2018154628A5 JP 2018154628 A5 JP2018154628 A5 JP 2018154628A5 JP 2018088769 A JP2018088769 A JP 2018088769A JP 2018088769 A JP2018088769 A JP 2018088769A JP 2018154628 A5 JP2018154628 A5 JP 2018154628A5
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amino acid
acid sequence
polypeptide
seq
disease
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JP6768027B2 (ja
JP2018154628A (ja
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Claims (10)

  1. 少なくとも1つの第一の免疫グロブリン単一可変ドメイン(ISV)および少なくとも1つの第二の免疫グロブリン単一可変ドメイン(ISV)を含むポリペプチドであって、ヒトのIL-17A、ヒトのIL-17Fおよび/またはヒトのIL-17A/Fに特異的に結合し、
    ここで、第一のISVは、
    a)(i)アミノ酸配列SYVVG(配列番号222)または(ii)アミノ酸配列SYVVG(配列番号222)と1個のアミノ酸相違しか有さないアミノ酸配列のいずれかであるCDR1;
    b)(i)アミノ酸配列AISGSGDSIYYAVSEKD(配列番号364)または(ii)アミノ酸配列AISGSGESIYYAVSEKG(配列番号364)と3個までのアミノ酸相違しか有さないアミノ酸配列のいずれかであるCDR2;および
    c)(i)アミノ酸配列DQEFGYLRFGRSEY(配列番号506)または(ii)アミノ酸配列DQEFGYLRFGRSEY(配列番号506)と3個までのアミノ酸相違しか有さないアミノ酸配列のいずれかであるCDR3;
    を含み、および、
    第二のISVが、
    a)アミノ酸配列AMG(配列番号238)を含むCDR1;
    b)(i)アミノ酸配列AISGSGDDTYYADSVKG(配列番号380)または(ii)アミノ酸配列AISATGDDTYYADSVKG(配列番号380)と3個までのアミノ酸相違しか有さないアミノ酸配列のいずれかを含むCDR2;および
    c)(i)アミノ酸配列RRGLYYVWDSNDYEN(配列番号522)または(ii)アミノ酸配列RRGLYYVWDANDYEN(配列番号522)と3個までのアミノ酸相違しか有さないアミノ酸配列のいずれかを含むCDR3
    を含む、前記ポリペプチド
  2. 請求項1に記載のポリペプチドであって、前記の特異的結合が、表面プラズモン共鳴(SPR)によって測定される場合、10 -3 -1 〜10 -6 -1 の解離速度(k off 速度)を特徴とする前記ポリペプチド。
  3. 請求項1または2に記載のポリペプチドであって、前記の特異的結合が、表面プラズモン共鳴(SPR)によって測定される場合、1nM未満のK D で生ずる前記ポリペプチド。
  4. 請求項1から3までのいずれか1項に記載のポリペプチドであって、前記のポリペプチドは、軽鎖可変ドメイン、重鎖可変ドメインおよび/または単一可変ドメインを含む、前記ポリペプチド。
  5. 請求項1から4までのいずれか1項に記載のポリペプチドであって、前記のポリペプチドは、野生型のヒトIL-17F配列への結合と比較して大きく低減された親和性でIL-17F突然変異体へ結合し、IL-17F突然変異体は、R47A、I86AおよびN89Aの1以上を含む、前記ポリペプチド。
  6. 請求項1から5までのいずれか1項に記載のポリペプチドであって、前記のポリペプチドは、野生型のヒトIL-17A配列への結合と比較して大きく低減された親和性でIL-17F突然変異体へ結合し、IL-17F突然変異体は、L74A、Y85AおよびN88Aの1以上を含む、前記ポリペプチド。
  7. 請求項1から6までのいずれか1項に記載のポリペプチドであって、前記のポリペプチドは、配列番号836のアミノ酸配列において、1個から10個までのアミノ酸置換、欠失、および/または挿入を含んでいる、前記ポリペプチド。
  8. 配列番号836のアミノ酸配列を含む、請求項1から7のいずれか1項に記載のポリペプチド。
  9. 請求項1から8までのいずれか1項に記載のポリペプチドであって、全身性エリテマトーデス、リウマチ様関節炎、変形性関節症、若年性慢性関節炎、脊椎関節症、全身性硬化症、突発性炎症性筋疾患、シェーグレン症候群、全身性血管炎、サルコイドーシス、自己免疫性溶血性貧血、自己免疫性血小板減少症、甲状腺炎、糖尿病、免疫介在性腎疾患、中枢神経系および末梢神経系の脱髄疾患、多発性硬化症、突発性脱髄性多発根神経炎、ギラン・バレー症候群、慢性炎症性脱髄性多発根神経炎、肝胆道系疾患、感染性自己免疫性慢性活動性肝炎、原発性胆汁性肝硬変、肉芽腫性肝炎、硬化性胆管炎、炎症性腸疾患、グルテン過敏性腸疾患、ウィップル病、自己免疫性もしくは免疫介在性の皮膚病、水疱性皮膚病、多形性紅斑、接触皮膚炎、乾癬、アレルギー疾患、喘息、アレルギー性鼻炎、アトピー性皮膚炎、食物過敏症、蕁麻疹、好酸球性肺炎、突発性肺線維症、過敏性肺炎、移植関連疾患、移植片拒絶および移植片対宿主病からなる群より選択される疾患または障害の治療のための前記ポリペプチド。
  10. 請求項1から8までのいずれか1項に記載のポリペプチドと製剤学的に認容性の賦形剤とを含む医薬組成物。
JP2018088769A 2011-05-05 2018-05-02 Il−17a、il−17fおよび/またはil17−a/fに対するアミノ酸配列および前記アミノ酸配列を含むポリペプチド Active JP6768027B2 (ja)

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JP2018088769A Active JP6768027B2 (ja) 2011-05-05 2018-05-02 Il−17a、il−17fおよび/またはil17−a/fに対するアミノ酸配列および前記アミノ酸配列を含むポリペプチド
JP2020084866A Active JP7093380B2 (ja) 2011-05-05 2020-05-14 Il-17a、il-17fおよび/またはil17-a/fに対するアミノ酸配列および前記アミノ酸配列を含むポリペプチド
JP2022097718A Pending JP2022137058A (ja) 2011-05-05 2022-06-17 Il-17a、il-17fおよび/またはil17-a/fに対するアミノ酸配列および前記アミノ酸配列を含むポリペプチド
JP2024083267A Pending JP2024122989A (ja) 2011-05-05 2024-05-22 Il-17a、il-17fおよび/またはil17-a/fに対するアミノ酸配列および前記アミノ酸配列を含むポリペプチド

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JP2022097718A Pending JP2022137058A (ja) 2011-05-05 2022-06-17 Il-17a、il-17fおよび/またはil17-a/fに対するアミノ酸配列および前記アミノ酸配列を含むポリペプチド
JP2024083267A Pending JP2024122989A (ja) 2011-05-05 2024-05-22 Il-17a、il-17fおよび/またはil17-a/fに対するアミノ酸配列および前記アミノ酸配列を含むポリペプチド

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US (4) US10017568B2 (ja)
EP (3) EP4105231A1 (ja)
JP (5) JP6628965B2 (ja)
KR (1) KR102083230B1 (ja)
CN (2) CN107098971B (ja)
AU (1) AU2012257942B8 (ja)
BR (1) BR112013028407B1 (ja)
CA (1) CA2834907C (ja)
CL (1) CL2013003090A1 (ja)
DK (1) DK2705058T3 (ja)
EA (1) EA035973B9 (ja)
ES (1) ES2662371T3 (ja)
HR (1) HRP20180380T1 (ja)
HU (1) HUE037225T2 (ja)
IL (1) IL228813B (ja)
LT (1) LT2705058T (ja)
MX (1) MX2013012844A (ja)
MY (1) MY167231A (ja)
NZ (1) NZ616761A (ja)
PT (1) PT2705058T (ja)
SG (2) SG10201606409TA (ja)
SI (1) SI2705058T1 (ja)
UA (1) UA117218C2 (ja)
WO (1) WO2012156219A1 (ja)

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