JP2020519600A5 - - Google Patents

Download PDF

Info

Publication number
JP2020519600A5
JP2020519600A5 JP2019561766A JP2019561766A JP2020519600A5 JP 2020519600 A5 JP2020519600 A5 JP 2020519600A5 JP 2019561766 A JP2019561766 A JP 2019561766A JP 2019561766 A JP2019561766 A JP 2019561766A JP 2020519600 A5 JP2020519600 A5 JP 2020519600A5
Authority
JP
Japan
Prior art keywords
peripheral blood
ibrutinib
pbl
lymphoma
culture medium
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2019561766A
Other languages
English (en)
Other versions
JP7349365B2 (ja
JP2020519600A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2018/032109 external-priority patent/WO2018209115A1/en
Publication of JP2020519600A publication Critical patent/JP2020519600A/ja
Publication of JP2020519600A5 publication Critical patent/JP2020519600A5/ja
Priority to JP2023147115A priority Critical patent/JP2023182601A/ja
Application granted granted Critical
Publication of JP7349365B2 publication Critical patent/JP7349365B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Claims (22)

  1. 末梢血から末梢血リンパ球(PBL)を拡大培養する方法であって、
    )イブルチニブ又は別のインターロイキン−2誘導性T細胞キナーゼ(ITK)で前処置され、且つイブルチニブ又は当該別のITK阻害剤での処置に抵抗性である患者の末梢血から得られた末梢血単核細胞(PBMC)のサンプルを、IL−2及び抗CD3/抗CD28抗体を有する第1の培養培地を含む培養物で培養し、それにより前記PBMCから末梢血リンパ球(PBL)の拡大培養を行うステップ;
    (b)ステップ(a)の培養物から前記PBLを回収するステップ、を含み、
    前記方法が約9日間、約10日間、約11日間、約12日間、約13日間及び約14日間から成る群から選択される期間にわたって実施される、方法。
  2. ステップ(a)の前に、前記PBMCがCD19+選択に供されて、前記PBMCがCD19+PBMC及び非CD19+PBMCに分離され、ステップ(a)が非CD19+PBMCを培養することにより実施される、請求項1に記載の方法。
  3. ステップ(a)において、抗CD3/抗CD28抗体が磁気ビーズに結合されており、前記ビーズと細胞との比が培養物において3:1である、請求項1又は2に記載の方法。
  4. ステップ(a)において、前記PBMCの培養の4日目に追加のIL−2が培養物に添加され、第1の培養培地が培養物中で交換される、請求項1又は2に記載の方法。
  5. ステップ(a)における磁気ビーズがDynabeads(商標)である、請求項3に記載の方法
  6. 第1の培養培地が培養物中で第2の培養培地に交換され、任意選択により、第1の培養培地が第2の培養培地と異なり、任意選択により、第1の培養培地がCM−2であり、第2の培養培地がCM−4である、請求項4に記載の方法。
  7. 末梢血が血液悪性腫瘍に罹患している患者の末梢血に由来する、請求項1〜6のいずれか一項に記載の方法。
  8. 血液悪性腫瘍が液性腫瘍である、請求項7に記載の方法。
  9. 液性腫瘍が白血病である、請求項8に記載の方法。
  10. 液性腫瘍が慢性リンパ性リンパ腫である、請求項9に記載の方法。
  11. 第1の培養培地が約3000IU/mlのIL−2を含み、そして/あるいは培養物が37℃、5%CO でインキュベートされる、請求項1又は2に記載の方法。
  12. 前記方法が約9日間にわたり実施されるか、又は前記方法が約11日間にわたり実施される、請求項1又は2に記載の方法。
  13. 前記患者がイブルチニブで前処置され、且つイブルチニブでの処置に抵抗性である、請求項1又は2に記載の方法。
  14. 前記患者がイブルチニブで少なくとも3ヶ月前処置される、請求項13に記載の方法。
  15. イブルチニブ又は別のITKで前処置される前に少なくとも1ヶ月イブルチニブ又は前記別のITK阻害剤での処置を受けていない、請求項1又は2に記載の方法。
  16. 血液悪性腫瘍の治療における使用のため末梢血リンパ球(PBL)であって、請求項1〜15のいずれか一項に記載の方法によって得られる、末梢血リンパ球(PBL)。
  17. 末梢血リンパ球(PBL)が、イブルチニブで前処置されており、且つイブルチニブでの処置に抵抗性である患者への投与のためのものであり、任意選択により、前記患者が少なくとも3ラウンドのイブルチニブレジメンで前処置され、任意選択により、前記患者が少なくとも3ヶ月イブルチニブで前処置される、請求項16に記載の末梢血リンパ球(PBL)。
  18. 末梢血リンパ球(PBL)が、イブルチニブ又は別のITKで前処置される前に少なくとも1ヶ月イブルチニブ又は前記別のITK阻害剤での処置を受けていない患者への投与のためのものである、請求項16に記載の末梢血リンパ球(PBL)。
  19. 血液悪性腫瘍が急性骨髄性白血病(AML)、マントル細胞リンパ腫(MCL)、濾胞性リンパ腫(FL)、びまん性大細胞型B細胞リンパ腫(DLBCL)、活性化B細胞(ABC)DLBCL、胚中心B細胞(GCB)DLBCL、慢性リンパ性白血病(CLL)、小リンパ球性白血病(SLL)、非ホジキンリンパ腫(NHL)、ホジキンリンパ腫、再発性及び/又は難治性ホジキンリンパ腫、B細胞急性リンパ芽球性白血病(B−ALL)、成熟B−ALL、バーキットリンパ腫、ワルデンストローム型マクログロブリン血症(WM)、多発性骨髄腫、骨髄異形成症候群、骨髄線維症、慢性骨髄性白血病、濾胞中枢リンパ腫、無痛性NHL、ヒト免疫不全ウイルス(HIV)関連B細胞リンパ腫並びにエプスタイン−バーウイルス(EBV)関連B細胞リンパ腫からなる群から選択される、請求項16に記載の末梢血リンパ球(PBL)。
  20. 血液悪性腫瘍が液性腫瘍である、請求項16に記載の末梢血リンパ球(PBL)
    方法
  21. 液性腫瘍が白血病である、請求項19に記載の末梢血リンパ球(PBL)。
  22. 液性腫瘍が慢性リンパ性リンパ腫である、請求項20に記載の末梢血リンパ球(PBL)。
JP2019561766A 2017-05-10 2018-05-10 液性腫瘍からの腫瘍浸潤リンパ球の拡大培養及びその治療的使用 Active JP7349365B2 (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2023147115A JP2023182601A (ja) 2017-05-10 2023-09-11 液性腫瘍からの腫瘍浸潤リンパ球の拡大培養及びその治療的使用

Applications Claiming Priority (15)

Application Number Priority Date Filing Date Title
US201762504337P 2017-05-10 2017-05-10
US62/504,337 2017-05-10
US201762530681P 2017-07-10 2017-07-10
US62/530,681 2017-07-10
US201762550398P 2017-08-25 2017-08-25
US62/550,398 2017-08-25
US201762590034P 2017-11-22 2017-11-22
US62/590,034 2017-11-22
US201862621462P 2018-01-24 2018-01-24
US62/621,462 2018-01-24
US201862621798P 2018-01-25 2018-01-25
US62/621,798 2018-01-25
US201862647367P 2018-03-23 2018-03-23
US62/647,367 2018-03-23
PCT/US2018/032109 WO2018209115A1 (en) 2017-05-10 2018-05-10 Expansion of tumor infiltrating lymphocytes from liquid tumors and therapeutic uses thereof

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2023147115A Division JP2023182601A (ja) 2017-05-10 2023-09-11 液性腫瘍からの腫瘍浸潤リンパ球の拡大培養及びその治療的使用

Publications (3)

Publication Number Publication Date
JP2020519600A JP2020519600A (ja) 2020-07-02
JP2020519600A5 true JP2020519600A5 (ja) 2021-07-26
JP7349365B2 JP7349365B2 (ja) 2023-09-22

Family

ID=62685090

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2019561766A Active JP7349365B2 (ja) 2017-05-10 2018-05-10 液性腫瘍からの腫瘍浸潤リンパ球の拡大培養及びその治療的使用
JP2023147115A Pending JP2023182601A (ja) 2017-05-10 2023-09-11 液性腫瘍からの腫瘍浸潤リンパ球の拡大培養及びその治療的使用

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2023147115A Pending JP2023182601A (ja) 2017-05-10 2023-09-11 液性腫瘍からの腫瘍浸潤リンパ球の拡大培養及びその治療的使用

Country Status (14)

Country Link
US (4) US20200224161A1 (ja)
EP (1) EP3622055A1 (ja)
JP (2) JP7349365B2 (ja)
KR (1) KR20200003913A (ja)
CN (1) CN110832070A (ja)
AU (1) AU2018266202A1 (ja)
BR (1) BR112019023409A2 (ja)
CA (1) CA3062874A1 (ja)
CR (1) CR20190557A (ja)
MA (1) MA50871A (ja)
MX (1) MX2019013202A (ja)
PH (1) PH12019502528A1 (ja)
TW (1) TW201904578A (ja)
WO (1) WO2018209115A1 (ja)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201522097D0 (en) 2015-12-15 2016-01-27 Cellular Therapeutics Ltd Cells
AU2017292889A1 (en) 2016-07-07 2019-02-14 Iovance Biotherapeutics, Inc. Programmed death 1 Ligand 1 (PD-L1) binding proteins and methods of use thereof
DK3532607T3 (da) 2016-10-26 2024-04-02 Iovance Biotherapeutics Inc Restimulation af kryokonserverede, tumorinfiltrerende lymfocytter
GB201700621D0 (en) 2017-01-13 2017-03-01 Guest Ryan Dominic Method,device and kit for the aseptic isolation,enrichment and stabilsation of cells from mammalian solid tissue
EP3596108A4 (en) 2017-03-15 2020-12-23 Pandion Operations, Inc. TARGETED IMMUNOTOLERANCE
JOP20190224A1 (ar) 2017-03-29 2019-09-26 Iovance Biotherapeutics Inc عمليات من أجل إنتاج الخلايا اللمفاوية المرتشحة للأورام واستخداماتها في العلاج المناعي
US11254913B1 (en) 2017-03-29 2022-02-22 Iovance Biotherapeutics, Inc. Processes for production of tumor infiltrating lymphocytes and uses of same in immunotherapy
JP2020521452A (ja) 2017-05-24 2020-07-27 パンディオン・セラピューティクス・インコーポレイテッド 標的化免疫寛容
WO2018226714A1 (en) 2017-06-05 2018-12-13 Iovance Biotherapeutics, Inc. Methods of using tumor infiltrating lymphocytes in double-refractory melanoma
US10174092B1 (en) 2017-12-06 2019-01-08 Pandion Therapeutics, Inc. IL-2 muteins
US10946068B2 (en) 2017-12-06 2021-03-16 Pandion Operations, Inc. IL-2 muteins and uses thereof
US11713446B2 (en) 2018-01-08 2023-08-01 Iovance Biotherapeutics, Inc. Processes for generating TIL products enriched for tumor antigen-specific T-cells
EP3765094A4 (en) 2018-03-15 2021-12-22 KSQ Therapeutics, Inc. GENE REGULATION COMPOSITIONS AND METHODS FOR IMPROVING IMMUNOTHERAPY
MX2020011134A (es) 2018-04-27 2020-11-11 Iovance Biotherapeutics Inc Proceso cerrado para expansion y edicion de genes de linfocitos infiltrantes de tumor y usos de los mismos en inmunoterapia.
WO2019217753A1 (en) * 2018-05-10 2019-11-14 Iovance Biotherapeutics, Inc. Processes for production of tumor infiltrating lymphocytes and uses of same in immunotherapy
CN109536444B (zh) * 2018-12-11 2022-06-28 吉林省拓华生物科技有限公司 一种适用于恶性实体瘤肿瘤浸润t淋巴细胞的分离诱导方法
AU2020279240A1 (en) 2019-05-20 2021-12-23 Pandion Operations, Inc. MAdCAM targeted immunotolerance
KR20220119439A (ko) 2019-12-20 2022-08-29 인스틸 바이오 유케이 리미티드 종양 침윤 림프구를 분리하기 위한 장치 및 방법 및 그것의 용도
EP4107187A1 (en) 2020-02-21 2022-12-28 Pandion Operations, Inc. Tissue targeted immunotolerance with a cd39 effector
WO2022017217A1 (zh) * 2020-07-24 2022-01-27 四川大学华西医院 一种靶向ebv的同种异体b细胞疫苗及其制备方法
EP4225330A1 (en) * 2020-10-06 2023-08-16 Iovance Biotherapeutics, Inc. Treatment of nsclc patients with tumor infiltrating lymphocyte therapies
WO2022076606A1 (en) * 2020-10-06 2022-04-14 Iovance Biotherapeutics, Inc. Treatment of nsclc patients with tumor infiltrating lymphocyte therapies
WO2022078305A1 (zh) * 2020-10-12 2022-04-21 四川海思科制药有限公司 一种杂环衍生物及其在医药上的应用
WO2022125941A1 (en) * 2020-12-11 2022-06-16 Iovance Biotherapeutics, Inc. Treatment of cancer patients with tumor infiltrating lymphocyte therapies in combination with braf inhibitors and/or mek inhibitors
CA3202473A1 (en) 2020-12-17 2022-06-23 Friedrich Graf Finckenstein Treatment of cancers with tumor infiltrating lymphocytes
JP2023554395A (ja) 2020-12-17 2023-12-27 アイオバンス バイオセラピューティクス,インコーポレイテッド Ctla-4及びpd-1阻害剤と併用した腫瘍浸潤リンパ球療法による治療
TW202242085A (zh) 2020-12-31 2022-11-01 美商艾歐凡斯生物治療公司 供自動生產腫瘤浸潤淋巴球的裝置和方法
CN114908050B (zh) * 2021-02-08 2024-05-07 苏州沙砾生物科技有限公司 肿瘤浸润淋巴细胞的制备方法及其用途
JP2024507929A (ja) 2021-02-25 2024-02-21 アラウノス セラピューティクス インコーポレイテッド 多シストロン性発現カセットを含む組換えベクター及びそれらの使用方法
WO2022187741A2 (en) 2021-03-05 2022-09-09 Iovance Biotherapeutics, Inc. Tumor storage and cell culture compositions
EP4314253A2 (en) 2021-03-25 2024-02-07 Iovance Biotherapeutics, Inc. Methods and compositions for t-cell coculture potency assays and use with cell therapy products
WO2022225981A2 (en) 2021-04-19 2022-10-27 Iovance Biotherapeutics, Inc. Chimeric costimulatory receptors, chemokine receptors, and the use of same in cellular immunotherapies
EP4340850A1 (en) 2021-05-17 2024-03-27 Iovance Biotherapeutics, Inc. Pd-1 gene-edited tumor infiltrating lymphocytes and uses of same in immunotherapy
TW202327631A (zh) 2021-07-28 2023-07-16 美商艾歐凡斯生物治療公司 利用腫瘤浸潤性淋巴球療法與kras抑制劑組合治療癌症患者
IL311333A (en) 2021-09-09 2024-05-01 Iovance Biotherapeutics Inc Processes for the production of TIL products using a strong PD-1 TALEN
WO2023049862A1 (en) 2021-09-24 2023-03-30 Iovance Biotherapeutics, Inc. Expansion processes and agents for tumor infiltrating lymphocytes
TW202331735A (zh) * 2021-10-27 2023-08-01 美商艾歐凡斯生物治療公司 協調用於患者特異性免疫療法之細胞之製造的系統及方法
AU2022388729A1 (en) 2021-11-10 2024-05-16 Iovance Biotherapeutics, Inc. Methods of expansion treatment utilizing cd8 tumor infiltrating lymphocytes
WO2023147486A1 (en) 2022-01-28 2023-08-03 Iovance Biotherapeutics, Inc. Tumor infiltrating lymphocytes engineered to express payloads
WO2023201369A1 (en) 2022-04-15 2023-10-19 Iovance Biotherapeutics, Inc. Til expansion processes using specific cytokine combinations and/or akti treatment
WO2023219873A1 (en) * 2022-05-10 2023-11-16 H. Lee Moffitt Cancer Center And Research Institute, Inc. Methods of culturing tumor infiltrating lymphocytes
WO2024011114A1 (en) 2022-07-06 2024-01-11 Iovance Biotherapeutics, Inc. Devices and processes for automated production of tumor infiltrating lymphocytes
WO2024030758A1 (en) 2022-08-01 2024-02-08 Iovance Biotherapeutics, Inc. Chimeric costimulatory receptors, chemokine receptors, and the use of same in cellular immunotherapies
WO2024098027A1 (en) 2022-11-04 2024-05-10 Iovance Biotherapeutics, Inc. Methods for tumor infiltrating lymphocyte (til) expansion related to cd39/cd103 selection

Family Cites Families (82)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0154316B1 (en) 1984-03-06 1989-09-13 Takeda Chemical Industries, Ltd. Chemically modified lymphokine and production thereof
US4766106A (en) 1985-06-26 1988-08-23 Cetus Corporation Solubilization of proteins for pharmaceutical compositions using polymer conjugation
US5206344A (en) 1985-06-26 1993-04-27 Cetus Oncology Corporation Interleukin-2 muteins and polymer conjugation thereof
JP3101690B2 (ja) 1987-03-18 2000-10-23 エス・ビィ・2・インコーポレイテッド 変性抗体の、または変性抗体に関する改良
US6780613B1 (en) 1988-10-28 2004-08-24 Genentech, Inc. Growth hormone variants
DE68925966T2 (de) 1988-12-22 1996-08-29 Kirin Amgen Inc Chemisch modifizierte granulocytenkolonie erregender faktor
US4902502A (en) 1989-01-23 1990-02-20 Cetus Corporation Preparation of a polymer/interleukin-2 conjugate
US5089261A (en) 1989-01-23 1992-02-18 Cetus Corporation Preparation of a polymer/interleukin-2 conjugate
DE3920358A1 (de) 1989-06-22 1991-01-17 Behringwerke Ag Bispezifische und oligospezifische, mono- und oligovalente antikoerperkonstrukte, ihre herstellung und verwendung
WO1993011161A1 (en) 1991-11-25 1993-06-10 Enzon, Inc. Multivalent antigen-binding proteins
US5714350A (en) 1992-03-09 1998-02-03 Protein Design Labs, Inc. Increasing antibody affinity by altering glycosylation in the immunoglobulin variable region
DE4447484C2 (de) 1994-04-08 1997-07-17 Deutsches Krebsforsch Mittel zur Hemmung von Apoptose
GB9422383D0 (en) 1994-11-05 1995-01-04 Wellcome Found Antibodies
US6121022A (en) 1995-04-14 2000-09-19 Genentech, Inc. Altered polypeptides with increased half-life
US6096871A (en) 1995-04-14 2000-08-01 Genentech, Inc. Polypeptides altered to contain an epitope from the Fc region of an IgG molecule for increased half-life
US5739277A (en) 1995-04-14 1998-04-14 Genentech Inc. Altered polypeptides with increased half-life
US5869046A (en) 1995-04-14 1999-02-09 Genentech, Inc. Altered polypeptides with increased half-life
JP2001506967A (ja) 1996-08-02 2001-05-29 ブリストル―マイヤーズ・スクイブ・カンパニー 治療およびインビボ診断における免疫グロブリンの使用の結果としての免疫グロブリン誘発毒性の抑制方法
WO1998023289A1 (en) 1996-11-27 1998-06-04 The General Hospital Corporation MODULATION OF IgG BINDING TO FcRn
US6277375B1 (en) 1997-03-03 2001-08-21 Board Of Regents, The University Of Texas System Immunoglobulin-like domains with increased half-lives
US6242195B1 (en) 1998-04-02 2001-06-05 Genentech, Inc. Methods for determining binding of an analyte to a receptor
US6194551B1 (en) 1998-04-02 2001-02-27 Genentech, Inc. Polypeptide variants
PT1068241E (pt) 1998-04-02 2007-11-19 Genentech Inc Variantes de anticorpos e respectivos fragmentos
US6528624B1 (en) 1998-04-02 2003-03-04 Genentech, Inc. Polypeptide variants
DK2180007T4 (da) 1998-04-20 2017-11-27 Roche Glycart Ag Glycosyleringsteknik for antistoffer til forbedring af antistofafhængig cellecytotoxicitet
GB9809951D0 (en) 1998-05-08 1998-07-08 Univ Cambridge Tech Binding molecules
CA2341029A1 (en) 1998-08-17 2000-02-24 Abgenix, Inc. Generation of modified molecules with increased serum half-lives
EP1006183A1 (en) 1998-12-03 2000-06-07 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Recombinant soluble Fc receptors
US6737056B1 (en) 1999-01-15 2004-05-18 Genentech, Inc. Polypeptide variants with altered effector function
MXPA01007170A (es) 1999-01-15 2002-07-30 Genentech Inc Variantes de polipeptidos con funcion efectora alterada.
EP2275540B1 (en) 1999-04-09 2016-03-23 Kyowa Hakko Kirin Co., Ltd. Method for controlling the activity of immunologically functional molecule
US7541184B2 (en) * 2000-02-24 2009-06-02 Invitrogen Corporation Activation and expansion of cells
JP3904374B2 (ja) 2000-02-29 2007-04-11 独立行政法人科学技術振興機構 キラー活性を増強したリンパ球
JP2004534721A (ja) 2000-10-31 2004-11-18 ピーアール ファーマシューティカルズ,インク. 生理活性分子の向上した送達のための方法及び組成物
GB0029407D0 (en) 2000-12-01 2001-01-17 Affitech As Product
EP2357187A1 (en) 2000-12-12 2011-08-17 MedImmune, LLC Molecules with extended half-lives, compositions and uses thereof
BR0213761A (pt) 2001-10-25 2005-04-12 Genentech Inc Composições, preparação farmacêutica, artigo industrializado, método de tratamento de mamìferos, célula hospedeira, método para a produção de uma glicoproteìna e uso da composição
US20040002587A1 (en) 2002-02-20 2004-01-01 Watkins Jeffry D. Fc region variants
JP2006502091A (ja) 2002-03-01 2006-01-19 イミューノメディクス、インコーポレイテッド クリアランス速度を高めるための二重特異性抗体点変異
US20040132101A1 (en) 2002-09-27 2004-07-08 Xencor Optimized Fc variants and methods for their generation
WO2003085107A1 (fr) 2002-04-09 2003-10-16 Kyowa Hakko Kogyo Co., Ltd. Cellules à génome modifié
ATE536188T1 (de) 2002-08-14 2011-12-15 Macrogenics Inc Fcgammariib-spezifische antikörper und verfahren zur verwendung davon
WO2004029207A2 (en) 2002-09-27 2004-04-08 Xencor Inc. Optimized fc variants and methods for their generation
SI1562972T1 (sl) 2002-10-15 2010-12-31 Facet Biotech Corp ALTERACIJA FcRn VEZANIH AFINITET ALI SERUMSKIH RAZPOLOVNIH DOB ANTITELESC Z MUTAGENEZO
US7355008B2 (en) 2003-01-09 2008-04-08 Macrogenics, Inc. Identification and engineering of antibodies with variant Fc regions and methods of using same
CN101120083B (zh) 2003-10-08 2013-03-27 威尔森沃尔夫制造公司 利用透气性材料进行细胞培养的方法及装置
GB0324368D0 (en) 2003-10-17 2003-11-19 Univ Cambridge Tech Polypeptides including modified constant regions
WO2005077981A2 (en) 2003-12-22 2005-08-25 Xencor, Inc. Fc POLYPEPTIDES WITH NOVEL Fc LIGAND BINDING SITES
KR101149242B1 (ko) 2004-01-12 2012-05-25 어플라이드 몰리큘라 에볼류션, 인코포레이티드 Fc 영역 변이체
EP2053062A1 (en) 2004-03-24 2009-04-29 Xencor, Inc. Immunoglobin variants outside the Fc region
DE102004014983A1 (de) 2004-03-26 2005-10-20 Univ Stuttgart Rekombinante Polypeptide der Mitglieder der TNF Ligandenfamilie und deren Verwendung
WO2005123780A2 (en) 2004-04-09 2005-12-29 Protein Design Labs, Inc. Alteration of fcrn binding affinities or serum half-lives of antibodies by mutagenesis
WO2006085967A2 (en) 2004-07-09 2006-08-17 Xencor, Inc. OPTIMIZED ANTI-CD20 MONOCONAL ANTIBODIES HAVING Fc VARIANTS
WO2006019447A1 (en) 2004-07-15 2006-02-23 Xencor, Inc. Optimized fc variants
WO2006047350A2 (en) 2004-10-21 2006-05-04 Xencor, Inc. IgG IMMUNOGLOBULIN VARIANTS WITH OPTIMIZED EFFECTOR FUNCTION
WO2007136790A2 (en) 2006-05-18 2007-11-29 Mannkind Corporation Intracellular kinase inhibitors
EP1894940A1 (en) 2006-08-28 2008-03-05 Apogenix GmbH TNF superfamily fusion proteins
CA2963124C (en) 2007-07-10 2019-10-15 Apogenix Ag Tnf superfamily collectin fusion proteins
EP2310409A2 (en) 2008-06-17 2011-04-20 Apogenix GmbH Multimeric tnf receptors
US8450460B2 (en) 2008-07-21 2013-05-28 Apogenix Gmbh Single-chain TNFSF fusion polypeptides
EP2364152A4 (en) 2008-11-03 2013-02-13 Univ Johns Hopkins METHOD FOR PRODUCING AND USING MARKINFILTRATING LYMPHOCYTES (MILS)
WO2010078966A1 (en) 2009-01-09 2010-07-15 Apogenix Gmbh Fusion proteins forming trimers
EP2408769A1 (en) 2009-03-17 2012-01-25 Glaxo Group Limited Pyrimidine derivatives used as itk inhibitors
US20130115617A1 (en) 2009-12-08 2013-05-09 John R. Wilson Methods of cell culture for adoptive cell therapy
US8956860B2 (en) 2009-12-08 2015-02-17 Juan F. Vera Methods of cell culture for adoptive cell therapy
SG181559A1 (en) 2009-12-08 2012-07-30 Wolf Wilson Mfg Corp Improved methods of cell culture for adoptive cell therapy
CA3144697A1 (en) 2010-11-12 2012-05-18 Nektar Therapeutics Conjugates of an il-2 moiety and a polymer
PL3214091T3 (pl) * 2010-12-09 2019-03-29 The Trustees Of The University Of Pennsylvania Zastosowanie komórek T modyfikowanych chimerycznymi receptorami antygenowymi do leczenia nowotworów
US20120244133A1 (en) 2011-03-22 2012-09-27 The United States of America, as represented by the Secretary, Department of Health and Methods of growing tumor infiltrating lymphocytes in gas-permeable containers
JP6386447B2 (ja) 2012-05-18 2018-09-05 ウィルソン ウォルフ マニュファクチャリング コーポレイションWilson Wolf Manufacturing Corporation 養子細胞療法のための改良された細胞培養法
WO2013188427A1 (en) 2012-06-11 2013-12-19 Wilson Wolf Manufacturing Corporation Improved methods of cell culture for adoptive cell therapy
US20150361150A1 (en) * 2013-02-04 2015-12-17 Roger Williams Medical Center Methods and compositions for treating gastrointestinal stromal tumor (gist)
RU2671897C2 (ru) 2013-03-01 2018-11-07 Дзе Юнайтед Стейтс Оф Америка, Эз Репрезентед Бай Дзе Секретари, Департмент Оф Хелс Энд Хьюман Сёрвисез Способы получения из опухоли обогащенных популяций реактивных в отношении опухоли т-клеток
AU2014302589B2 (en) 2013-06-24 2020-05-14 Wilson Wolf Manufacturing, LLC Closed system device and methods for gas permeable cell culture process
WO2015112847A1 (en) 2014-01-24 2015-07-30 Confluence Life Sciences, Inc. Arylpyridinone itk inhibitors for treating inflammation and cancer
SG10202109752XA (en) * 2014-04-07 2021-10-28 Novartis Ag Treatment of cancer using anti-cd19 chimeric antigen receptor
BR112016028996A2 (pt) 2014-06-11 2018-01-30 Polybiocept Ab composição para expansão de linfócitos; método de preparação de uma população de linfócitos clinicamente relevantes; imunoterapia para tratamento ou prevenção de uma doença infecciosa, uma doença cancerígena, ou uma doença autoimune em um mamífero; composição para uso; kit para uso em imunoterapia, em particular, para tratamento de uma doença cancerígena; linfócito clinicamente relevante obtido por um método; e população de linfócitos clinicamente relevantes obtida por um método
US9531689B1 (en) 2014-11-10 2016-12-27 The United States Of America As Represented By The Secretary Of The Navy System and method for encryption of network data
EP3034092A1 (en) * 2014-12-17 2016-06-22 Université de Lausanne Adoptive immunotherapy for treating cancer
MX2017009571A (es) 2015-01-23 2018-09-27 Aclaris Therapeutics Inc Inhibidores heterociclicos de itk para el tratamiento de la inflamacion y cancer.
MA42902A (fr) * 2015-07-08 2018-05-16 Univ Johns Hopkins Lymphocytes infiltrant la moelle (mil) en tant que source de lymphocytes t pour une thérapie par des récepteurs chimériques d'un antigène (car)
US11590167B2 (en) * 2016-12-03 2023-02-28 Juno Therapeutic, Inc. Methods and compositions for use of therapeutic T cells in combination with kinase inhibitors

Similar Documents

Publication Publication Date Title
JP2020519600A5 (ja)
Makita et al. Clinical development of anti‐CD 19 chimeric antigen receptor T‐cell therapy for B‐cell non‐Hodgkin lymphoma
Shanbhag et al. Hodgkin lymphoma: A review and update on recent progress
JP6215394B2 (ja) エクスビボ培養されたナチュラルキラー細胞の集団
Duan et al. The BCMA-targeted fourth-generation CAR-T cells secreting IL-7 and CCL19 for therapy of refractory/recurrent multiple myeloma
Berrien-Elliott et al. Improving natural killer cell cancer immunotherapy
RU2017134652A (ru) Cd20 терапия, cd22 терапия и комбинированная терапия клетками, экспрессирующими химерный антигенный рецептор (car) k cd19
Park et al. Interleukin-21 increases direct cytotoxicity and IFN-γ production of ex vivo expanded NK cells towards breast cancer cells
Rubnitz et al. Natural killer cell therapy in children with relapsed leukemia
Mata-Molanes et al. Cancer immunotherapy with cytokine-induced killer cells
JPH10179151A (ja) 二特異的抗体を用いた幹細胞移植における汚染腫瘍細胞の除去
Hoseini et al. Bispecific antibody does not induce T-cell death mediated by chimeric antigen receptor against disialoganglioside GD2
Baragano Raneros et al. Acute myeloid leukemia and NK cells: two warriors confront each other
Berdeja et al. Systemic interleukin-2 and adoptive transfer of lymphokine-activated killer cells improves antibody-dependent cellular cytotoxicity in patients with relapsed B-cell lymphoma treated with rituximab
Cappuzzello et al. Retargeting cytokine-induced killer cell activity by CD16 engagement with clinical-grade antibodies
JP2020533362A5 (ja)
Snauwaert et al. Can immunotherapy specifically target acute myeloid leukemic stem cells?
Turtle et al. Therapy of B cell malignancies with CD19-specific chimeric antigen receptor-modified T cells of defined subset composition
Whiteside Human tumor-infiltrating lymphocytes and their characterization
Schuster et al. Phase IIa trial of chimeric antigen receptor modified T cells directed against CD19 (CTL019) in patients with relapsed or refractory CD19+ lymphomas
Bonyhadi et al. In vitro engagement of CD3 and CD28 corrects T cell defects in chronic lymphocytic leukemia
Zhang et al. IL-6/IFN-γ double knockdown CAR-T cells reduce the release of multiple cytokines from PBMCs in vitro
Nadal et al. Adjuvant interleukin-2 therapy for patients refractory to donor lymphocyte infusions
Pupa et al. Activation of mononuclear cells to be used for hybrid monoclonal antibody‐induced lysis of human ovarian carcinoma cells
Teoh et al. Developing lisocabtagene maraleucel chimeric antigen receptor T-cell manufacturing for improved process, product quality and consistency across CD19+ hematologic indications