Thymic Determinants of γδ T Cell Differentiation

被引:104
|
作者
Munoz-Ruiz, Miguel [1 ]
Sumaria, Nital [2 ]
Pennington, Daniel J. [2 ]
Silva-Santos, Bruno [1 ]
机构
[1] Univ Lisbon, Fac Med, Inst Med Mol, Lisbon, Portugal
[2] Queen Mary Univ London, Barts & London Sch Med, Blizard Inst, London E1 2AT, England
基金
欧洲研究理事会; 英国惠康基金;
关键词
INNATE LYMPHOID-CELLS; TCR SIGNAL STRENGTH; ALPHA-BETA; TRANSCRIPTION FACTOR; INTERFERON-GAMMA; LINEAGE DIFFERENTIATION; ROR-GAMMA; RECEPTOR; SUBSETS; FATE;
D O I
10.1016/j.it.2017.01.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
gamma d T cells have emerged as major sources of the proinflammatory cytokines interleukin-17 (IL-17) and interferon-gamma (IFN gamma) in multiple models of infection, cancer and autoimmune disease. However, unlike their alpha beta T cell counterparts that require peripheral activation for effector cell differentiation, gamma delta T cells instead can be 'developmentally programmed' in the thymus to generate discrete gamma delta T cell effector subsets with distinctive molecular signatures. Nonetheless, recent studies have presented conflicting viewpoints on the signals involved in thymic gamma delta T cell development and differentiation, namely on the role of both T cell receptor (TCR)-dependent and TCR-independent factors. Here we review the current data and the ongoing controversies.
引用
收藏
页码:336 / 344
页数:9
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