Barral Duarte C, Brenner Michael B
Division of Rheumatology, Immunology and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, 1 Jimmy Fund Way, Boston, Massachusetts 02115, USA.
Nat Rev Immunol. 2007 Dec;7(12):929-41. doi: 10.1038/nri2191.
The classic concept of self-non-self discrimination by the immune system focused on the recognition of fragments from proteins presented by classical MHC molecules. However, the discovery of MHC-class-I-like CD1 antigen-presentation molecules now explains how the immune system also recognizes the abundant and diverse universe of lipid-containing antigens. The CD1 molecules bind and present amphipathic lipid antigens for recognition by T-cell receptors. Here, we outline the recent advances in our understanding of how the processes of CD1 assembly, trafficking, lipid-antigen binding and T-cell activation are achieved and the new insights into how lipid antigens differentially elicit CD1-restricted innate and adaptive T-cell responses.
免疫系统对自身与非自身进行区分的经典概念聚焦于对由经典MHC分子呈递的蛋白质片段的识别。然而,MHC-I类样CD1抗原呈递分子的发现,现在解释了免疫系统如何识别含脂质抗原这个丰富多样的世界。CD1分子结合并呈递两亲性脂质抗原以供T细胞受体识别。在此,我们概述了近期在理解CD1组装、转运、脂质抗原结合及T细胞激活过程如何实现方面取得的进展,以及脂质抗原如何差异性地引发CD1限制性固有和适应性T细胞反应的新见解。