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The CD4-centered universe of human T cell subsets
被引:73
|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.
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页码:252 / 262
页数:11
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