Metabolic Reprogramming in CD8+ T Cells During Acute Viral Infections

被引:25
作者
Gupta, Shubhranshu S. [1 ,2 ]
Wang, Jin [3 ,4 ]
Chen, Min [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Pathol & Immunol, Houston, TX 77030 USA
[2] Baylor Coll Med, Interdept Grad Program Translat Biol & Mol Med, Houston, TX 77030 USA
[3] Houston Methodist Res Inst, Immunobiol & Transplant Sci Ctr, Houston, TX USA
[4] Cornell Univ, Weill Cornell Med Coll, Dept Surg, New York, NY 10021 USA
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
关键词
CD8(+) T cells; metabolism; glycolysis; fatty acid oxidation; glutaminolysis; epigenetics; viral infections; TRANSCRIPTION FACTOR; MEMORY DIFFERENTIATION; AEROBIC GLYCOLYSIS; DEACETYLASE SIRT1; DNA METHYLATION; DENDRITIC CELLS; IL-15; ACTIVATION; AUTOPHAGY; COMPLEX;
D O I
10.3389/fimmu.2020.01013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD8(+) T cells represent one of the most versatile immune cells critical for clearing away viral infections. Due to their important role, CD8(+) T cell activation and memory formation during viral infection have been the focus of several studies recently. Although CD8(+) T cell activation and memory formation have been associated with metabolic alterations, the molecular understanding behind T cells choosing one type of metabolism over others based on their differentiation stage is still unclear. This review focuses on how the signaling molecules and cellular processes that are characteristic of CD8(+) T cell activation and memory formation also play a critical role in selecting specific type of metabolism during viral infections. In addition, we will summarize the epigenetic factors regulating these metabolic alterations.
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页数:11
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