首页> 外文期刊>The journal of immunology >Cutting Edge: CD1d Restriction and Th1/Th2/Th17 Cytokine Secretion by Human Vδ3 T Cells
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Cutting Edge: CD1d Restriction and Th1/Th2/Th17 Cytokine Secretion by Human Vδ3 T Cells

机译:前沿:人类Vδ3T细胞对CD1d的限制和Th1 / Th2 / Th17细胞因子的分泌

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Human γδ T cells expressing the Vδ3 TCR make up a minor lymphocyte subset in blood but are enriched in liver and in patients with some chronic viral infections and leukemias. We analyzed the frequencies, phenotypes, restriction elements, and functions of fresh and expanded peripheral blood Vδ3 T cells. Vδ3 T cells accounted for ~0.2% of circulating T cells, included CD4+, CD8+, and CD4?CD8? subsets, and variably expressed CD56, CD161, HLA-DR, and NKG2D but neither NKG2A nor NKG2C. Vδ3 T cells were sorted and expanded by mitogen stimulation in the presence of IL-2. Expanded Vδ3 T cells recognized CD1d but not CD1a, CD1b, or CD1c. Upon activation, they killed CD1d+ target cells, released Th1, Th2, and Th17 cytokines, and induced maturation of dendritic cells into APCs. Thus, Vδ3 T cells are glycolipid-reactive T cells with distinct Ag specificities but functional similarities to NKT cells.
机译:表达Vδ3TCR的人γδT细胞在血液中构成次要的淋巴细胞亚群,但在肝脏以及患有某些慢性病毒感染和白血病的患者中富集。我们分析了新鲜和扩展的外周血Vδ3T细胞的频率,表型,限制元件和功能。 Vδ3T细胞约占循环T细胞的0.2%,包括CD4 +,CD8 +和CD4?CD8?。亚基,并可变表达CD56,CD161,HLA-DR和NKG2D,但NKG2A和NKG2C均不表达。 Vδ3T细胞在IL-2存在下通过有丝分裂原刺激进行分选和扩增。扩增的Vδ3T细胞识别CD1d,但不能识别CD1a,CD1b或CD1c。激活后,它们杀死CD1d +目标细胞,释放Th1,Th2和Th17细胞因子,并诱导树突状细胞成熟为APC。因此,Vδ3T细胞是糖脂反应性T细胞,具有不同的Ag特异性但与NKT细胞功能相似。

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