T细胞
免疫系统
CD8型
封锁
细胞生物学
癌症研究
细胞溶解
肿瘤微环境
细胞毒性T细胞
细胞生长
生物
化学
生物化学
肿瘤细胞
免疫学
受体
体外
作者
Mei‐Chun Lin,Sofie Hedlund Møller,Ping‐Chih Ho
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2023-12-12
卷期号:13 (12): 2507-2509
被引量:1
标识
DOI:10.1158/2159-8290.cd-23-1059
摘要
Summary: Rowe and colleagues discover that one-carbon (1C) metabolism rewiring occurs upon T-cell activation to support proliferation and cytolytic activity in CD8+ T cells and that supplementation of 1C donor formate rescues the dysfunctional T cells and their responsiveness to anti–PD-1 in selective tumor-infiltrated T-cell subsets. This finding represents an attractive strategy to overcome a metabolic vulnerability in the tumor microenvironment and improve the efficacy of immune checkpoint blockade. See related article by Rowe et al., p. 2566 (8).
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