Epigenetic Maintenance of Acquired Gene Expression Programs during Memory CD8 T Cell Homeostasis

被引:24
|
作者
Abdelsamed, Hossam A. [1 ]
Zebley, Caitlin C. [1 ,2 ]
Youngblood, Ben [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, 332 N Lauderdale St, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Oncol, 332 N Lauderdale St, Memphis, TN 38105 USA
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 9卷
基金
美国国家卫生研究院;
关键词
epigenetic regulation; CD8 T cells; homeostasis; immunological memory; cytokines; LINEAGE RELATIONSHIP; IFN-GAMMA; NAIVE; IL-15; PROLIFERATION; EFFECTOR; SURVIVAL; PHENOTYPE; DIFFERENTIATION; DEMETHYLATION;
D O I
10.3389/fimmu.2018.00006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory CD8 T cells have a unique ability to provide lifelong immunity against pathogens containing their cognate epitope. Because of their ability to provide lifelong protection, the generation of memory T cells is now a major focus for current vaccination or adoptive cell therapy approaches to treat chronic viral infections and cancer. It is now clear that maintenance of memory CD8 T cells occurs through a process of antigen-independent homeostatic proliferation, which is regulated in part by the gamma chain cytokines IL-7 and IL-15. Here, we will describe the role of these cytokines in the survival and self-renewal of memory CD8 T cells. Further, we will describe the role of epigenetics in the maintenance of acquired functions among memory CD8 T cells during homeostatic proliferation.
引用
收藏
页数:8
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