Transcriptional programming of tissue-resident memory CD8+ T cells

被引:86
|
作者
Milner, J. Justin [1 ]
Goldrath, Ananda W. [1 ]
机构
[1] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
TUMOR-INFILTRATING LYMPHOCYTES; CUTTING EDGE; TERMINAL DIFFERENTIATION; PROMOTES DIFFERENTIATION; PROTECTIVE IMMUNITY; NONLYMPHOID TISSUES; TGF-BETA; EFFECTOR; INFECTION; MIGRATION;
D O I
10.1016/j.coi.2018.03.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tissue-resident memory CD8(+) T cells (T-RM) are localized in non-lymphoid tissues throughout the body where they mediate long-lived protective immunity at common sites of pathogen exposure. As the signals controlling T-RM differentiation are uncovered, it is becoming apparent that the dynamic activities of numerous transcription factors are intricately involved in T-RM formation. Here, we highlight known transcriptional regulators of T-RM differentiation and discuss how understanding the transcriptional programming of CD8(+) T cell residency in non-lymphoid tissues can be leveraged to prevent or treat disease.
引用
收藏
页码:162 / 169
页数:8
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