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Cell Metab ; 34(3): 378-395, 2022 03 01.
Article in English | MEDLINE | ID: covidwho-1712531

ABSTRACT

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.


Subject(s)
COVID-19 , Neoplasms , Virus Diseases , Aged , Aging , CD8-Positive T-Lymphocytes , Cell Differentiation , Epigenesis, Genetic , Humans , Neoplasms/metabolism , Virus Diseases/metabolism
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