Direct costimulatory effect of TLR3 ligand poly(I:C) on human γδ T lymphocytes

被引:142
作者
Wesch, D [1 ]
Beetz, S [1 ]
Oberg, HH [1 ]
Marget, M [1 ]
Krengel, K [1 ]
Kabelitz, D [1 ]
机构
[1] Univ Klinikum Schleswig Holstein, Inst Immunol, D-24105 Kiel, Germany
关键词
D O I
10.4049/jimmunol.176.3.1348
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
TLR3 recognizes viral dsRNA and its synthetic mimetic polyinosinic-polycytidylic acid (poly(I:C)). TLR3 expression is commonly considered to be restricted to dendritic cells, NK cells, and fibroblasts. In this study we report that human gamma delta and alpha beta T lymphocytes also express TLR3, as shown by quantitative real-time PCR, flow cytometry, and confocal microscopy. Although T cells did not respond directly to poly(I:C), we observed a dramatic increase in IFN-gamma secretion and an up-regulation of CD69 when freshly isolated gamma delta T cells were stimulated via TCR in the presence of poly(I:C) without APC. IFN-gamma secretion was partially inhibited by anti-TLR3 Abs. In contrast, poly(I:C) did not costimulate IFN-gamma secretion by alpha beta T cells. These results indicate that TLR3 signaling is differentially regulated in TCR-stimulated gamma delta and alpha beta T cells, suggesting an early activation of gamma delta T cells in antiviral immunity.
引用
收藏
页码:1348 / 1354
页数:7
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