How do CARs work? Early insights from recent clinical studies targeting CD19

被引:83
作者
Davila, Marco L. [1 ]
Brentjens, Renier [1 ]
Wang, Xiuyan [1 ]
Riviere, Isabelle [1 ]
Sadelain, Michel [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, Ctr Cell Engn, New York, NY 10021 USA
来源
ONCOIMMUNOLOGY | 2012年 / 1卷 / 09期
关键词
adoptive T-cell therapy; CD19; chimeric antigen receptors; gene therapy; CHIMERIC ANTIGEN RECEPTOR; CHRONIC LYMPHOCYTIC-LEUKEMIA; HUMAN T-CELLS; ADOPTIVE IMMUNOTHERAPY; ANTITUMOR-ACTIVITY; ENHANCED SURVIVAL; CD28; PERSISTENCE; EXPRESSION; LYMPHOMA;
D O I
10.4161/onci.22524
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Second-generation chimeric antigen receptors (CARs) are powerful tools to redirect antigen-specific T cells independently of HLA-restriction. Recent clinical studies evaluating CD19-targeted T cells in patients with B-cell malignancies demonstrate the potency of CAR-engineered T cells. With results from 28 subjects enrolled by five centers conducting studies in patients with chronic lymphocytic leukemia (CLL) or lymphoma, some insights into the parameters that determine T-cell function and clinical outcome of CAR-based approaches are emerging. These parameters involve CAR design, T-cell production methods, conditioning chemotherapy as well as patient selection. Here, we discuss the potential relevance of these findings and in particular the interplay between the adoptive transfer of T cells and pre-transfer patient conditioning.
引用
收藏
页码:1577 / 1583
页数:7
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