The CD4-centered universe of human T cell subsets

被引:74
作者
Geginat, J. [1 ]
Paroni, M. [1 ]
Facciotti, F. [1 ]
Gruarin, P. [1 ]
Kastirr, I. [1 ]
Caprioli, F. [2 ,3 ]
Pagani, M. [1 ]
Abrignani, S. [1 ]
机构
[1] INGM, Autoimmun Program, I-20122 Milan, Italy
[2] Univ Milan, Dept Pathophysiol & Transplantat, I-20122 Milan, Italy
[3] Osped Policlin, Fdn IRCCS Ca Granda, Unit Gastroenterol 2, Milan, Italy
关键词
CD4(+) memory T cells; T cell differentiation; Cytokines; Tissue homing; GROWTH-FACTOR-BETA; CHEMOKINE RECEPTOR EXPRESSION; CYTOKINE GENE-EXPRESSION; PRODUCE IFN-GAMMA; LATENT TGF-BETA; TRANSCRIPTION FACTOR; TH17; CELLS; CENTRAL MEMORY; IL-7; RECEPTOR; HELPER-CELLS;
D O I
10.1016/j.smim.2013.10.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Humans are continuously exposed to a high number of diverse pathogens that induce different types of immune responses. Primary pathogen-specific immune responses generate multiple subsets of memory T cells, which provide protection against secondary infections. In recent years, several novel T cell subsets have been identified and have significantly broadened our knowledge about T cell differentiation and the regulation of immune responses. At the same time the rapidly growing number of incompletely characterized T cell subsets has also generated some controversies. We therefore review here the current knowledge on features and functions of human alpha/beta T cell subsets, focusing on CD4(+) T cells classified according to cytokine production and tissue localization. The principal helper and regulatory T cell subsets can be identified by a limited number of relevant surface markers, which are an integral part of the T cell differentiation programs because they are directly induced by the relevant lineage-defining transcription factors. In vivo occurring human T cell subsets can thus be purified directly ex vivo from relevant tissues for molecular and functional studies, and represent not only an ideal model to study T cell differentiation, but they also offer important clinical opportunities. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:252 / 262
页数:11
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