Human T Cell Development, Localization, and Function throughout Life

被引:904
作者
Kumar, Brahma V. [1 ]
Connors, Thomas J. [1 ,4 ]
Farber, Donna L. [1 ,2 ,3 ]
机构
[1] Columbia Univ, Med Ctr, Columbia Ctr Translat Immunol, New York, NY 10032 USA
[2] Columbia Univ, Med Ctr, Dept Surg, New York, NY 10032 USA
[3] Columbia Univ, Med Ctr, Dept Microbiol & Immunol, New York, NY 10032 USA
[4] Columbia Univ, Med Ctr, Dept Pediat, New York, NY 10032 USA
关键词
RECENT THYMIC EMIGRANTS; EFFECTOR MEMORY CELLS; IMMUNE RECONSTITUTION; NEONATAL THYMECTOMY; DIGEORGE-SYNDROME; LYMPHOID ORGANS; DENDRITIC CELLS; BONE-MARROW; RESIDENT; TISSUE;
D O I
10.1016/j.immuni.2018.01.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Throughout life, T cells coordinate multiple aspects of adaptive immunity, including responses to pathogens, allergens, and tumors. In mouse models, the role of T cells is studied in the context of a specific type of pathogen, antigen, or disease condition over a limited time frame, whereas in humans, T cells control multiple insults simultaneously throughout the body and maintain immune homeostasis over decades. In this review, we discuss how human T cells develop and provide essential immune protection at different life stages and highlight tissue localization and subset delineation as key determinants of the T cell functional role in immune responses. We also discuss how anatomic compartments undergo distinct age-associated changes in T cell subset composition and function over a lifetime. It is important to consider age and tissue influences on human T cells when developing targeted strategies to modulate T cell-mediated immunity in vaccines and immunotherapies.
引用
收藏
页码:202 / 213
页数:12
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