CAR models: next-generation CAR modifications for enhanced T-cell function

被引:122
作者
Abate-Daga, Daniel [1 ,2 ,3 ]
Davila, Marco L. [3 ,4 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Immunol, Tampa, FL 33612 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Dept Cutaneous Oncol, Tampa, FL 33612 USA
[3] Univ S Florida, Morsani Coll Med, Tampa, FL 33620 USA
[4] H Lee Moffitt Canc Ctr & Res Inst, Dept Blood & Marrow Transplantat, Tampa, FL USA
来源
MOLECULAR THERAPY-ONCOLYTICS | 2016年 / 3卷
关键词
CHIMERIC-ANTIGEN-RECEPTOR; ADOPTIVE IMMUNOTHERAPY; ANTITUMOR-ACTIVITY; CD28; COSTIMULATION; SPACER DOMAIN; ZETA-CHAIN; CANCER; TUMORS; INTERLEUKIN-12; PERSISTENCE;
D O I
10.1038/mto.2016.14
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
T cells genetically targeted with a chimeric antigen receptor (CAR) to B-cell malignancies have demonstrated tremendous clinical outcomes. With the proof in principle for CAR T cells as a therapy for B-cell malignancies being established, current and future research is being focused on adapting CAR technology to other cancers, as well as enhancing its efficacy and/or safety. The modular nature of the CAR, extracellular antigen-binding domain fused to a transmembrane domain and intracellular T-cell signaling domains, allows for optimization by replacement of the various components. These modifications are creating a whole new class of therapeutic CARs. In this review, we discuss the recent major advances in CAR design and how these modifications will impact its clinical application.
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页数:7
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