Center for Cell-Based Therapy, National Cancer Institute (NCI).
Surgery Branch, National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, Maryland 20892, USA.
Nat Rev Immunol. 2018 May;18(5):340-356. doi: 10.1038/nri.2017.146. Epub 2018 Jan 30.
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.
在受到刺激时,少量的幼稚 CD8 T 细胞会增殖并分化为多种记忆和效应细胞类型。CD8 T 细胞可以持续存在多年,并杀死肿瘤细胞和受病毒感染的细胞。CD8 T 细胞分化过程中发生的功能和表型变化已经得到很好的描述,但这些变化背后的表观遗传状态还不完全清楚。在这里,我们回顾了指导 CD8 T 细胞分化和功能的表观遗传过程。我们专注于基因及其调控元件上 DNA 和相关组蛋白的表观遗传修饰。我们还描述了影响基因表达的染色质组织的结构变化。最后,我们研究了表观遗传干预在改善慢性感染和癌症个体中 CD8 T 细胞功能方面的转化潜力。
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