Tissue-specific differentiation of CD8+ resident memory T cells

被引:35
|
作者
Yang, Kun [1 ,2 ]
Kallies, Axel [3 ]
机构
[1] Beijing Hosp, Dept Dermatol, Natl Ctr Gerontol, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Inst Geriatr Med, Beijing, Peoples R China
[3] Univ Melbourne, Peter Doherty Inst Infect & Immun, Melbourne, Vic 3000, Australia
基金
英国医学研究理事会;
关键词
TGF-BETA; NONLYMPHOID TISSUES; BONE-MARROW; LYMPH-NODE; RM CELLS; EFFECTOR; INFECTION; PROMOTES; IMMUNITY; MAINTENANCE;
D O I
10.1016/j.it.2021.08.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD8(+) tissue-resident memory T (T-RM) cells play crucial roles in defense against infections and cancer and have been implicated in autoimmune diseases such as psoriasis. In mice and humans, they exist in all nonlymphoid organs and share key characteristics across all tissues, including downregulation of tissue egress and lymph node homing pathways. However, recent studies demonstrate considerable heterogeneity across T-RM cells lodged in different tissues - linked to the activity of tissue-specific molecules, including chemokines, cytokines, and transcription factors. Current work indicates that transforming growth factor (TGF)-beta plays a major role in generating T-RM heterogeneity at phenotypic and functional levels. Here, we review common and unique features of T-RM cells in different tissues and discuss putative strategies aimed at harnessing T-RM cells for site-specific protection against infectious and malignant diseases.
引用
收藏
页码:876 / 890
页数:15
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