Mixing signals: molecular turn ons and turn offs for innate γδ T-cells

被引:10
作者
Bekiaris, Vasileios [1 ]
Sedy, John R. [1 ]
Ware, Carl F. [1 ]
机构
[1] Sanford Burnham Med Res Inst, Infect & Inflammatory Dis Ctr, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
BTLA; dermatitis; gamma delta T-cell; IL-7; lymphotoxin; ROR gamma t; HERPESVIRUS ENTRY MEDIATOR; INTERLEUKIN-7; RECEPTOR; ALPHA-BETA; TRANSCRIPTION FACTORS; SKIN INFLAMMATION; INTERFERON-GAMMA; IMMUNE-RESPONSES; DENDRITIC CELLS; B-LYMPHOCYTE; ROR-GAMMA;
D O I
10.3389/fimmu.2014.00654
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lymphocytes of the gamma delta (gamma delta)-cell lineage are evolutionary conserved and although they express rearranged antigen-specific receptors, a large proportion respond as innate effectors. gamma delta T-cells are poised to combat infection by responding rapidly to cytokine stimuli similar to innate lymphoid cells. This potential to initiate strong inflammatory responses necessitates that inhibitory signals are balanced with activation signals. Here, we discuss some of the key mechanisms that regulate the development, activation, and inhibition of innate gamma delta T-cells in light of recent evidence that the inhibitory immunoglobulin-superfamily member B and T lymphocyte attenuator restricts their differentiation and effector function.
引用
收藏
页数:7
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