Combination Immunotherapy with CAR T Cells and Checkpoint Blockade for the Treatment of Solid Tumors

被引:343
|
作者
Grosser, Rachel [1 ]
Cherkassky, Leonid [2 ]
Chintala, Navin [1 ]
Adusumilli, Prasad S. [1 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, Thorac Serv, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc, Dept Surg, Surg Oncol Serv, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Ctr Cell Engn, New York, NY 10065 USA
关键词
PD-1; BLOCKADE; ANTITUMOR-ACTIVITY; CANCER-IMMUNOTHERAPY; ESTABLISHED TUMORS; ANTI-PD-1; ANTIBODY; CLINICAL ACTIVITY; HOST IMMUNITY; ANTIGEN; RECEPTOR; EXPRESSION;
D O I
10.1016/j.ccell.2019.09.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Checkpoint blockade (CPB) therapy can elicit durable clinical responses by reactivating an exhausted immune response. However, response rates remain limited, likely secondary to a lack of a tumor-reactive immune infiltrate. Chimeric antigen receptor (CAR) T cells may provide the necessary tumor-targeting immune infiltrate and a highly specific antitumor immune response. This can be further amplified by the addition of CPB agents, which serve to counteract the immune inhibitory environment undermining optimal CAR T cell efficacy. Herein, we review preclinical and clinical combination therapy with CAR T cells and CPB agents, with a focus on solid tumor malignancies.
引用
收藏
页码:471 / 482
页数:12
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