嵌合抗原受体
肿瘤微环境
免疫疗法
癌症
癌症研究
恶性肿瘤
T细胞
癌细胞
癌症治疗
细胞疗法
支柱
医学
细胞
生物
免疫学
肿瘤细胞
免疫系统
内科学
遗传学
结构工程
工程类
作者
Jhan-Jie Peng,Limei Wang,Zhiyu Li,Cheng‐Lung Ku,Ping‐Chih Ho
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2023-04-14
卷期号:8 (82)
被引量:38
标识
DOI:10.1126/sciimmunol.abq3016
摘要
Chimeric antigen receptor (CAR) T cells have achieved true clinical success in treating hematological malignancy patients, laying the foundation of CAR T cells as a new pillar of cancer therapy. Although these promising effects have generated strong interest in expanding the treatment of CAR T cells to solid tumors, reproducible demonstration of clinical efficacy in the setting of solid tumors has remained challenging to date. Here, we review how metabolic stress and signaling in the tumor microenvironment, including intrinsic determinants of response to CAR T cell therapy and extrinsic obstacles, restrict the efficacy of CAR T cell therapy in cancer treatment. In addition, we discuss the use of novel approaches to target and rewire metabolic programming for CAR T cell manufacturing. Last, we summarize strategies that aim to improve the metabolic adaptability of CAR T cells to enhance their potency in mounting antitumor responses and survival within the tumor microenvironment.
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