T细胞受体
刺激
细胞生物学
主要组织相容性复合体
转基因
T细胞
生物
转基因小鼠
肽
免疫学
抗原
免疫系统
基因
神经科学
生物化学
作者
Andrea L. Szymczak-Workman,Creg J. Workman,Dario A.A. Vignali
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2009-04-21
卷期号:182 (9): 5188-5192
被引量:67
标识
DOI:10.4049/jimmunol.0803123
摘要
Abstract The mechanism and stimulatory requirements of regulatory T cell (Treg)-mediated suppression are still unclear. To assess the requirement for Treg stimulation by cognate peptide:MHC, we used T cells from OTII and AND TCR transgenic mice that are specific for and restricted by distinct, noncrossreactive peptide:MHC combinations. This allowed us to independently activate Tregs and their conventional T cell (Tconv) targets. Surprisingly, we found that suppression can occur in the absence of peptide:MHC-mediated stimulation of Tregs. This suppression was Treg dependent and not due to cold target inhibition. Using Rag1−/− TCR transgenic T cells, we show that regulation of Tconv proliferation by heterogeneous Tregs is not due to alloreactivity or crossreactivity. Finally, using anti-TCR-Vβ8-coated microbeads and Vβ8− Tregs, we show that TCR stimulation-independent suppression can occur in the absence of APCs. These data suggest that Tregs may possess constitutive regulatory activity that can be mediated in the absence of cognate peptide:MHC-TCR stimulation.
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