表观遗传学
神经发生的表观遗传调控
生物
染色质
组蛋白
细胞分化
细胞毒性T细胞
CD8型
表型
细胞生物学
效应器
染色质重塑
遗传学
免疫系统
基因
体外
作者
Amanda N. Henning,Rahul Roychoudhuri,Nicholas P. Restifo
出处
期刊:Nature Reviews Immunology
[Springer Nature]
日期:2018-01-30
卷期号:18 (5): 340-356
被引量:379
摘要
CD8+T cell differentiation and function are regulated by epigenetic changes mainly including DNA methylation, histone modification and modification of chromatin architecture. As described here, a detailed understanding of these epigenetic mechanisms can be harnessed to improve T cell-based immunotherapies. Upon stimulation, small numbers of naive CD8+ T cells proliferate and differentiate into a variety of memory and effector cell types. CD8+ T cells can persist for years and kill tumour cells and virally infected cells. The functional and phenotypic changes that occur during CD8+ T cell differentiation are well characterized, but the epigenetic states that underlie these changes are incompletely understood. Here, we review the epigenetic processes that direct CD8+ T cell differentiation and function. We focus on epigenetic modification of DNA and associated histones at genes and their regulatory elements. We also describe structural changes in chromatin organization that affect gene expression. Finally, we examine the translational potential of epigenetic interventions to improve CD8+ T cell function in individuals with chronic infections and cancer.
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