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A class of γδ T cell receptors recognize the underside of the antigen-presenting molecule MR1

机译:一类γδT细胞受体识别抗原呈递分子MR1的底面

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T cell receptors (TCRs) recognize antigens presented by major histocompatibility complex (MHC) and MHC class I-like molecules. We describe a diverse population of human gamma delta T cells isolated from peripheral blood and tissues that exhibit autoreactivity to the monomorphic MHC-related protein 1 (MR1). The crystal structure of a gamma delta TCR-MR1-antigen complex starkly contrasts with all other TCR-MHC and TCR-MHC-I-like complex structures. Namely, the gamma delta TCR binds underneath the MR1 antigen-binding cleft, where contacts are dominated by the MR1 alpha 3 domain. A similar pattern of reactivity was observed for diverse MRl-restricted gamma delta TCRs from multiple individuals. Accordingly, we simultaneously report MR1 as a ligand for human gamma delta T cells and redefine the parameters for TCR recognition.
机译:T细胞受体(TCR)识别主要组织相容性复合物(MHC)和I类MHC分子呈递的抗原。我们描述了从外周血和组织中表现出对单态性MHC相关蛋白1(MR1)的自身反应性的人类伽玛三角洲T细胞的多样化人群。 γ-δTCR-MR1抗原复合物的晶体结构与所有其他TCR-MHC和TCR-MHC-1样复合物结构形成鲜明对比。即,γ-δTCR在MR1抗原结合裂隙下方结合,其中接触以MR1 alpha 3结构域为主。对于来自多个个体的各种MR1限制的γ-δTCR,观察到相似的反应模式。因此,我们同时报告了MR1作为人类伽马T细胞的配体,并重新定义了TCR识别参数。

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