Tissue-Resident Memory T Cells and Fixed Immune Surveillance in Nonlymphoid Organs

被引:94
|
作者
Carbone, Francis R. [1 ]
机构
[1] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Microbiol & Immunol, Melbourne, Vic 3010, Australia
来源
JOURNAL OF IMMUNOLOGY | 2015年 / 195卷 / 01期
关键词
HERPES-SIMPLEX-VIRUS; CUTTING EDGE; E-CADHERIN; PROMOTES DIFFERENTIATION; CD103; EXPRESSION; EPITHELIAL-CELLS; EFFERENT LYMPH; RM CELLS; SKIN; EFFECTOR;
D O I
10.4049/jimmunol.1500515
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell immunity is often defined in terms of memory lymphocytes that use the blood to access a range of organs. T cells are involved in two patterns of recirculation. In one, the cells shuttle back and forth between blood and secondary lymphoid organs, whereas in the second, memory cells recirculate between blood and nonlymphoid tissues. The latter is a means by which blood T cells control peripheral infection. It is now clear that there exists a distinct memory T cell subset that is absent from blood but found within nonlymphoid tissues. These nonrecirculating tissue-resident memory T (T-RM) cells develop within peripheral compartments and never spread beyond their point of lodgement. This review examines fixed immune surveillance by T-RM cells, highlighting features that make them potent controllers of infection in nonlymphoid tissues. These features provide clues about T-RM cell specialization, such as their ability to deal with sequestered, persisting infections confined to peripheral compartments.
引用
收藏
页码:17 / 22
页数:6
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