Anti-CD19 CAR T cells potently redirected to kill solid tumor cells

被引:17
作者
Ambrose, Christine [1 ]
Su, Lihe [1 ]
Wu, Lan [1 ]
Dufort, Fay J. [1 ]
Sanford, Thomas [1 ]
Birt, Alyssa [1 ]
Hackel, Benjamin J. [2 ]
Hombach, Andreas [3 ]
Abken, Hinrich [3 ,4 ]
Lobb, Roy R. [1 ]
Rennert, Paul D. [1 ]
机构
[1] Aleta Biotherapeut, Natick, MA 01760 USA
[2] Univ Minnesota, Minneapolis, MN USA
[3] Univ Cologne, Cologne, Germany
[4] Regensburg Univ, Regensburg, Germany
来源
PLOS ONE | 2021年 / 16卷 / 03期
关键词
CHIMERIC ANTIGEN RECEPTOR; B-CELLS; THERAPY; IMMUNOTHERAPY; ACTIVATION; CD19; LEUKEMIA; GLIOBLASTOMA; EXPRESSION; ANTIBODIES;
D O I
10.1371/journal.pone.0247701
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Successful CAR T cell therapy for the treatment of solid tumors requires exemplary CAR T cell expansion, persistence and fitness, and the ability to target tumor antigens safely. Here we address this constellation of critical attributes for successful cellular therapy by using integrated technologies that simplify development and derisk clinical translation. We have developed a CAR-CD19 T cell that secretes a CD19-anti-Her2 bridging protein. This cell therapy strategy exploits the ability of CD19-targeting CAR T cells to interact with CD19 on normal B cells to drive expansion, persistence and fitness. The secreted bridging protein potently binds to Her2-positive tumor cells, mediating CAR-CD19 T cell cytotoxicity in vitro and in vivo. Because of its short half-life, the secreted bridging protein will selectively accumulate at the site of highest antigen expression, ie. at the tumor. Bridging proteins that bind to multiple different tumor antigens have been created. Therefore, antigen-bridging CAR-CD19 T cells incorporate critical attributes for successful solid tumor cell therapy. This platform can be exploited to attack tumor antigens on any cancer.
引用
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页数:28
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共 80 条
[1]   HER2-Specific Chimeric Antigen Receptor-Modified Virus-Specific T Cells for Progressive Glioblastoma A Phase 1 Dose-Escalation Trial [J].
Ahmed, Nabil ;
Brawley, Vita ;
Hegde, Meenakshi ;
Bielamowicz, Kevin ;
Kalra, Mamta ;
Landi, Daniel ;
Robertson, Catherine ;
Gray, Tara L. ;
Diouf, Oumar ;
Wakefield, Amanda ;
Ghazi, Alexia ;
Gerken, Claudia ;
Yi, Zhongzhen ;
Ashoori, Aidin ;
Wu, Meng-Fen ;
Liu, Hao ;
Rooney, Cliona ;
Dotti, Gianpietro ;
Gee, Adrian ;
Su, Jack ;
Kew, Yvonne ;
Baskin, David ;
Zhang, Yi Jonathan ;
New, Pamela ;
Grilley, Bambi ;
Stojakovic, Milica ;
Hicks, John ;
Powell, Suzanne Z. ;
Brenner, Malcolm K. ;
Heslop, Helen E. ;
Grossman, Robert ;
Wels, Winfried S. ;
Gottschalk, Stephen .
JAMA ONCOLOGY, 2017, 3 (08) :1094-1101
[2]   Strategies to Address Chimeric Antigen Receptor Tonic Signaling [J].
Ajina, Adam ;
Maher, John .
MOLECULAR CANCER THERAPEUTICS, 2018, 17 (09) :1795-1815
[3]   CAR T cells for brain tumors: Lessons learned and road ahead [J].
Akhavan, David ;
Alizadeh, Darya ;
Wang, Dongrui ;
Weist, Michael R. ;
Shepphird, Jennifer K. ;
Brown, Christine E. .
IMMUNOLOGICAL REVIEWS, 2019, 290 (01) :60-84
[4]   Function of Novel Anti-CD19 Chimeric Antigen Receptors with Human Variable Regions Is Affected by Hinge and Transmembrane Domains [J].
Alabanza, Leah ;
Pegues, Melissa ;
Geldres, Claudia ;
Shi, Victoria ;
Wiltzius, Jed J. W. ;
Sievers, Stuart A. ;
Yang, Shicheng ;
Kochenderfer, James N. .
MOLECULAR THERAPY, 2017, 25 (11) :2452-2465
[5]   Adaptor CAR Platforms-Next Generation of T Cell-Based Cancer Immunotherapy [J].
Arndt, Claudia ;
Fasslrinner, Frederick ;
Loureiro, Liliana R. ;
Koristka, Stefanie ;
Feldmann, Anja ;
Bachmann, Michael .
CANCERS, 2020, 12 (05)
[6]   Multispecific Targeting with Synthetic Ankyrin Repeat Motif Chimeric Antigen Receptors [J].
Balakrishnan, Ashwini ;
Rajan, Anusha ;
Salter, Alexander I. ;
Kosasih, Paula L. ;
Wu, Qian ;
Voutsinas, Jenna ;
Jensen, Michael C. ;
Pluckthun, Andreas ;
Riddell, Stanley R. .
CLINICAL CANCER RESEARCH, 2019, 25 (24) :7506-7516
[7]   Nanobodies and Nanobody-Based Human Heavy Chain Antibodies As Antitumor Therapeutics [J].
Bannas, Peter ;
Hambach, Julia ;
Koch-Nolte, Friedrich .
FRONTIERS IN IMMUNOLOGY, 2017, 8
[8]   FDA Approval Summary: Axicabtagene Ciloleucel for Relapsed or Refractory Large B-cell Lymphoma [J].
Bouchkouj, Najat ;
Kasamon, Yvette L. ;
de Claro, R. Angelo ;
George, Bindu ;
Lin, Xue ;
Lee, Shiowjen ;
Blumenthal, Gideon M. ;
Bryan, Wilson ;
McKee, Amy E. ;
Pazdur, Richard .
CLINICAL CANCER RESEARCH, 2019, 25 (06) :1702-1708
[9]   Regression of Glioblastoma after Chimeric Antigen Receptor T-Cell Therapy [J].
Brown, Christine E. ;
Alizadeh, Darya ;
Starr, Renate ;
Weng, Lihong ;
Wagner, Jamie R. ;
Naranjo, Araceli ;
Ostberg, Julie R. ;
Blanchard, M. Suzette ;
Kilpatrick, Julie ;
Simpson, Jennifer ;
Kurien, Anita ;
Priceman, Saul J. ;
Wang, Xiuli ;
Harshbarger, Todd L. ;
D'Apuzzo, Massimo ;
Ressler, Julie A. ;
Jensen, Michael C. ;
Barish, Michael E. ;
Chen, Mike ;
Portnow, Jana ;
Forman, Stephen J. ;
Badie, Behnam .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 375 (26) :2561-2569
[10]   Adult Survivorship Considerations following CAR T-cell therapy [J].
Buitrago, Joaquin ;
Adkins, Sherry ;
Hawkins, Misha ;
Iyamu, Kharington ;
van Oort, Teresa .
CLINICAL JOURNAL OF ONCOLOGY NURSING, 2019, 23 (02) :42-48