Epigenetic regulation of T cell adaptive immunity

被引:14
|
作者
Frias, Adolfo B. [1 ]
Boi, Shannon K. [1 ]
Lan, Xin [1 ,2 ]
Youngblood, Ben [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[2] Univ Tennessee, Hlth Sci Ctr, Coll Grad Hlth Sci, Memphis, TN USA
关键词
DNA methylation; epigenetics; histone modifications; T cell differentiation; T cell exhaustion;
D O I
10.1111/imr.12943
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The conceptualization of adaptive immunity, founded on the observation of immunological memory, has served as the basis for modern vaccination and immunotherapy approaches. This fundamental concept has allowed immunologists to explore mechanisms that enable humoral and cellular lymphocytes to tailor immune response functions to a wide array of environmental insults and remain poised for future pathogenic encounters. Until recently, for T cells it has remained unclear how memory differentiation acquires and sustains a gene expression program that grants a cell with a capacity for a heightened recall response. Recent investigations into this critical question have identified epigenetic programs as a causal molecular mechanism governing T cell subset specification and immunological memory. Here, we outline the studies that have illustrated this concept and posit on how insights into T cell adaptive immunity can be applied to improve upon existing immunotherapies.
引用
收藏
页码:9 / 21
页数:13
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