Division of Cell Biology, La Jolla Institute for Allergy and Immunology, CA, USA.
Immunol Rev. 2012 Nov;250(1):167-79. doi: 10.1111/j.1600-065X.2012.01166.x.
Together with peptides, T lymphocytes respond to hydrophobic molecules, mostly lipids, presented by the non-classical CD1 family (CD1a-e). These molecules have evolved complex and diverse binding grooves in order to survey different cellular compartments for self and exogenous antigens, which are then presented for recognition to T-cell receptors (TCRs) on the surface of T cells. In particular, most CD1d-presented antigens are recognized by a population of lymphocytes denominated natural killer T (NKT) cells, characterized by a strong immunomodulatory potential. Among NKT cells, two major subsets (type I and type II NKT cells) have been described, based on their TCR repertoire and antigen specificity. Here we review recent structural and biochemical studies that have shed light on the molecular details of CD1d-mediated antigen recognition by type I and II NKT cells, which are in many aspects distinct from what has been observed for peptide major histocompatibility complex-reactive TCRs.
与肽一起,T 淋巴细胞对非经典 CD1 家族(CD1a-e)呈递的疏水分子,主要是脂质,产生应答。这些分子已经进化出复杂多样的结合槽,以便对自身和外源性抗原进行不同细胞区室的检测,然后将其呈递给 T 细胞表面的 T 细胞受体(TCR)进行识别。特别是,大多数由 CD1d 呈递的抗原被称为自然杀伤 T(NKT)细胞的一类淋巴细胞识别,其具有很强的免疫调节潜力。在 NKT 细胞中,根据其 TCR 库和抗原特异性,已经描述了两个主要亚群(I 型和 II 型 NKT 细胞)。在这里,我们综述了最近的结构和生化研究,这些研究阐明了 I 型和 II 型 NKT 细胞识别 CD1d 介导的抗原的分子细节,这些细节在许多方面与观察到的与肽主要组织相容性复合物反应性 TCR 不同。