表观遗传学
生物
重编程
细胞代谢
免疫
免疫系统
衰老
效应器
记忆T细胞
细胞
T细胞
后生
免疫学
细胞生物学
神经科学
DNA甲基化
遗传学
基因
基因表达
作者
Sofie Hedlund Møller,Pei‐Chun Hsueh,Yi-Ru Yu,Lianjun Zhang,Ping‐Chih Ho
标识
DOI:10.1016/j.cmet.2022.02.003
摘要
Productive T cell responses to infection and cancer rely on coordinated metabolic reprogramming and epigenetic remodeling among the immune cells. In particular, T cell effector and memory differentiation, exhaustion, and senescence/aging are tightly regulated by the metabolism-epigenetics axis. In this review, we summarize recent advances of how metabolic circuits combined with epigenetic changes dictate T cell fate decisions and shape their functional states. We also discuss how the metabolic-epigenetic axis orchestrates T cell exhaustion and explore how physiological factors, such as diet, gut microbiota, and the circadian clock, are integrated in shaping T cell epigenetic modifications and functionality. Furthermore, we summarize key features of the senescent/aged T cells and discuss how to ameliorate vaccination- and COVID-induced T cell dysfunctions by metabolic modulations. An in-depth understanding of the unexplored links between cellular metabolism and epigenetic modifications in various physiological or pathological contexts has the potential to uncover novel therapeutic strategies for fine-tuning T cell immunity.
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