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The functional plasticity of T cell subsets
被引:213
|作者:
Bluestone, Jeffrey A.
[1
,2
]
Mackay, Charles R.
[3
,4
,5
]
O'Shea, John J.
[6
]
Stockinger, Brigitta
[7
]
机构:
[1] Univ Calif San Francisco, Ctr Diabet, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[3] Monash Univ, Fac Med, Nursing & Hlth Serv, Clayton, Vic 3800, Australia
[4] Univ New S Wales, St Vincents Clin Sch, Sydney, NSW 2010, Australia
[5] Univ New S Wales, Garvan Inst Med Res, Sydney, NSW 2010, Australia
[6] NIAMSD, Mol Immunol & Inflammat Branch, US Natl Inst Hlth, Bethesda, MD 20892 USA
[7] Natl Inst Med Res, MRC, Div Mol Immunol, London NW7 1AA, England
基金:
英国医学研究理事会;
关键词:
FOLLICULAR-HELPER-CELLS;
ARYL-HYDROCARBON RECEPTOR;
TH17;
CELLS;
IN-VIVO;
INTERLEUKIN;
22;
CUTTING EDGE;
TGF-BETA;
DIFFERENTIATION;
LINEAGE;
GENERATION;
D O I:
10.1038/nri2654
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
In 1986, Robert Coffman and Timothy Mossman first described the division of CD4(+) T cells into functional subsets, termed T helper 1 (T(H)1) and T(H)2, based on cytokine production, and in doing so unwittingly opened a Pandora's box of complexity and controversy. Although the mechanisms that regulate T(H)1 and T(H)2 cells are now well known, recent descriptions of other CD4(+) T cell subsets-such as regulatory T cells, T follicular helper cells, T(H)17, T(H)22 and most recently T(H)9 and T(H)22 cells-have questioned how we think of T cell subsets and what commitment to a functional T cell subset means. Here, Nature Reviews Immunology asks four leaders in the field their thoughts on the functional plasticity of T cell subsets.
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页码:811 / 816
页数:6
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