JP2018064568A5 - - Google Patents

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JP2018064568A5
JP2018064568A5 JP2017223489A JP2017223489A JP2018064568A5 JP 2018064568 A5 JP2018064568 A5 JP 2018064568A5 JP 2017223489 A JP2017223489 A JP 2017223489A JP 2017223489 A JP2017223489 A JP 2017223489A JP 2018064568 A5 JP2018064568 A5 JP 2018064568A5
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pharmaceutical composition
truncated
nucleic acid
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JP6767347B2 (ja
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Claims (11)

  1. ヒトT細胞を含む医薬組成物であって、
    前記ヒトT細胞は:
    機能的PD−1細胞内ドメインを欠き、且つヒトT細胞におけるプログラム細胞死リガンド1(PD−L1)の阻害効果を減少させる切断型プログラム細胞死タンパク質1(PD−1)をコードする第1核酸;及び
    標的細胞の腫瘍抗原を認識する細胞外ドメイン、膜貫通ドメイン、並びにCD3−ゼータシグナルドメイン及び共刺激分子のシグナルドメインを含む細胞内ドメインを含むキメラ抗原受容体(CAR)をコードする第2核酸;
    を含み、
    前記切断型PD−1及び前記CARが別個のポリペプチドである遺伝子産物として発現される、医薬組成物
  2. 前記切断型PD−1は、ヒト細胞のヒトT細胞のPD−1と、特定の細胞のPD−L1との間の経路に干渉する、請求項1に記載の医薬組成物
  3. 前記切断型PD−1は、PD−1細胞外ドメイン若しくはPD−1膜貫通ドメイン又はそれらの組み合わせを含む、請求項1又は2に記載の医薬組成物
  4. 前記切断型PD−1は、配列番号9のアミノ酸配列若しくは配列番号10のアミノ酸配列又はそれらの組み合わせを含む、請求項1〜3のいずれか1項に記載の医薬組成物
  5. 前記切断型PD−1は、特定の細胞のPD−L1と結合するPD−1細胞外ドメインを含む可溶性受容体である、請求項1〜4のいずれか1項に記載の医薬組成物
  6. 前記腫瘍抗原がCD19である、請求項1〜5のいずれか1項に記載の医薬組成物
  7. 前記共刺激分子は、4−1BB若しくはCD28又はそれらの組み合わせを含む、請求項1〜6のいずれか1項に記載の医薬組成物
  8. 前記切断型PD−1は、配列番号12のアミノ酸配列、配列番号13のアミノ酸配列、又は配列番号14のアミノ酸配列を含む、請求項1〜7のいずれか1項に記載の医薬組成物
  9. 請求項1〜7のいずれか1項に記載の第1核酸及び第2核酸を含む、単離核酸
  10. 請求項9に記載の前記単離核酸含むベクター。
  11. 請求項に記載の前記単離核酸を含む、細胞。
JP2017223489A 2015-03-02 2017-11-21 Pd−l1によって誘導される免疫寛容の低減 Active JP6767347B2 (ja)

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US201562126804P 2015-03-02 2015-03-02
US62/126,804 2015-03-02

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US (4) US9572837B2 (ja)
EP (2) EP3549612A1 (ja)
JP (2) JP6336684B2 (ja)
KR (1) KR102133857B1 (ja)
CN (2) CN107073138B (ja)
AU (1) AU2016228080B2 (ja)
BR (1) BR112017018770A2 (ja)
CA (1) CA2976684C (ja)
RU (1) RU2688692C2 (ja)
SG (1) SG11201706947TA (ja)
WO (1) WO2016138846A1 (ja)

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