细胞毒性T细胞
CD8型
生物
肿瘤微环境
T细胞
表观基因组
免疫系统
癌症研究
过继性细胞移植
免疫
免疫疗法
免疫学
生物化学
体外
DNA甲基化
基因表达
基因
作者
Lianjun Zhang,Pedro Romero
标识
DOI:10.1016/j.molmed.2017.11.005
摘要
CD8+ T cells are central players in controlling infections and cancer. Longevity, functionality, and metabolic fitness are critical determinants of T cell efficacy in cancer immunotherapy. Tumor-infiltrating CD8+ T cells undergo metabolic 'exhaustion' in the nutrient- and oxygen-deprived tumor microenvironment (TME). Thus, reprograming CD8+ T cell metabolism may provide important therapeutic strategies for cancer treatment. Indeed, the adoptive transfer of memory CD8+ T cells with sustained metabolic fitness may yield better antitumor protection in both mouse models and the clinic. Here, we discuss recent progress on how cellular metabolism is linked to CD8+ T cell fate decisions and on how metabolic intermediates can impact gene expression via modulation of the epigenome. We examine the feasibility of developing potential strategies to improve antitumor immunity through the modulation of T cell metabolic activity.
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