Integrated Department of Immunology, National Jewish Health, Denver, CO 80206, USA.
Cell Mol Life Sci. 2011 Jul;68(14):2335-43. doi: 10.1007/s00018-011-0697-3. Epub 2011 May 8.
γδ T cells express adaptive antigen receptors encoded by rearranging genes. Their diversity is highest in the small region of TCR V-J junctions, especially in the δ chain, which should enable the γδ TCRs to distinguish differences in small epitopes. Indeed, recognition of small molecules, and of an epitope on a larger protein has been reported. Responses to small non-peptides known as phospho-antigens are multi-clonal yet limited to a single γδ T cell subset in humans and non-human primates. Responses to small peptides are multi-clonal or oligo-clonal, include more than one subset of γδ T cells, and occur in rodents and primates. However, less effort has been devoted to investigate the peptide responses. To settle the questions of whether peptides can be ligands for the γδ TCRs, and whether responses to small peptides might occur normally, peptide binding will have to be demonstrated, and natural peptide ligands identified.
γδ T 细胞表达由重排基因编码的适应性抗原受体。它们的多样性在 TCR V-J 连接处的小区域中最高,特别是在δ链中,这应该使 γδ TCR 能够区分小分子的差异。事实上,已经报道了对小分子和较大蛋白质上的表位的识别。对称为磷酸抗原的小非肽的反应是多克隆的,但仅限于人类和非人类灵长类动物中的单一 γδ T 细胞亚群。对小肽的反应是多克隆或寡克隆的,包括不止一个 γδ T 细胞亚群,并且发生在啮齿动物和灵长类动物中。然而,人们在研究肽反应方面的努力较少。为了解决肽是否可以作为 γδ TCR 的配体,以及对小肽的反应是否可能正常发生的问题,必须证明肽结合,并确定天然肽配体。