Functional development of γδ T cells

被引:171
作者
Prinz, Immo [1 ]
Silva-Santos, Bruno [2 ]
Pennington, Daniel J. [3 ]
机构
[1] Hannover Med Sch, Inst Immunol, D-30625 Hannover, Germany
[2] Univ Lisbon, Fac Med, Inst Mol Med, P-1699 Lisbon, Portugal
[3] Queen Mary Univ London, Blizard Inst, Barts & London Sch Med, London, England
基金
英国惠康基金; 欧洲研究理事会;
关键词
IFN-; IL-17; T-cell development; T-cell ontogeny; T-cell subsets; INTRAEPITHELIAL LYMPHOCYTES; IFN-GAMMA; INTERFERON-GAMMA; PROINFLAMMATORY IL-17(+); TCR REPERTOIRE; NKT CELLS; IN-VIVO; THYMUS; SUBSET; THYMOCYTES;
D O I
10.1002/eji.201343759
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The thymus generates T cells that are generally functionally immature and thus require peripheral activation for differentiation into effector lymphocytes. Notable exceptions to this rule are murine T cells, many of which have been shown to acquire their functional potential during thymic development from late embryonic stages. Here, we review the underlying ontogenic processes and molecular differentiation mechanisms of murine T cells, focusing on the transcriptional control of IFN- and IL-17 expression. We propose that functional commitment of T cells occurs in developmental windows defined by the molecular composition of the thymic microenvironment, such as T-cell receptor (TCR), TCR coreceptor ligands, and cytokines. We further discuss the similarities and particularities of functional development of T cells in mice and humans, while highlighting some key unresolved issues for future investigation.
引用
收藏
页码:1988 / 1994
页数:7
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