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人γδ T 细胞抗原受体与内皮蛋白 C 受体结合对巨细胞病毒和肿瘤应激的监测。

Cytomegalovirus and tumor stress surveillance by binding of a human γδ T cell antigen receptor to endothelial protein C receptor.

机构信息

Birmingham Cancer Research UK Cancer Centre, School of Cancer Sciences, University of Birmingham, Birmingham, UK.

出版信息

Nat Immunol. 2012 Sep;13(9):872-9. doi: 10.1038/ni.2394. Epub 2012 Aug 12.

Abstract

T cells bearing γδ T cell antigen receptors (TCRs) function in lymphoid stress surveillance. However, the contribution of γδ TCRs to such responses is unclear. Here we found that the TCR of a human V(γ)4V(δ)5 clone directly bound endothelial protein C receptor (EPCR), which allowed γδ T cells to recognize both endothelial cells targeted by cytomegalovirus and epithelial tumors. EPCR is a major histocompatibility complex-like molecule that binds lipids analogously to the antigen-presenting molecule CD1d. However, the V(γ)4V(δ)5 TCR bound EPCR independently of lipids, in an antibody-like way. Moreover, the recognition of target cells by γδ T cells required a multimolecular stress signature composed of EPCR and costimulatory ligand(s). Our results demonstrate how a γδ TCR mediates recognition of broadly stressed human cells by engaging a stress-regulated self antigen.

摘要

γδ T 细胞抗原受体 (TCR) 表达的 T 细胞在淋巴应激监测中发挥作用。然而,γδ TCR 在此类反应中的贡献尚不清楚。在这里,我们发现人类 V(γ)4V(δ)5 克隆的 TCR 可直接结合内皮蛋白 C 受体 (EPCR),使 γδ T 细胞能够识别巨细胞病毒靶向的内皮细胞和上皮肿瘤。EPCR 是一种主要组织相容性复合体样分子,它类似地结合脂质与抗原呈递分子 CD1d。然而,V(γ)4V(δ)5 TCR 以抗体样的方式独立于脂质结合 EPCR。此外,γδ T 细胞对靶细胞的识别需要由 EPCR 和共刺激配体组成的多分子应激特征。我们的结果表明,γδ TCR 如何通过结合应激调节的自身抗原来介导对广泛应激的人类细胞的识别。

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