4.6 Article

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

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JOURNAL OF IMMUNOLOGY
卷 176, 期 3, 页码 1348-1354

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.176.3.1348

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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.

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