Graduate Program in Immunology, Michigan Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Department of Microbiology and Immunology, Michigan Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Curr Opin Immunol. 2020 Jun;64:137-145. doi: 10.1016/j.coi.2020.05.008. Epub 2020 Jun 30.
The major histocompatibility class I (MHC-I) complex functions in innate and adaptive immunity, mediating surveillance of the subcellular environment. In humans, MHC-I heavy chains are encoded by three genes: the human leukocyte antigen (HLA)-A, HLA-B, and HLA-C. These genes are highly polymorphic, which results in the expression, typically, of six different HLA class I (HLA-I) proteins on the cell surface, and the presentation of diverse peptide antigens to CD8 T cells for broad surveillance against many pathogenic conditions. Recent studies of HLA-B allotypes show that the polymorphisms, not surprisingly, also significantly impact protein folding and assembly pathways. The use of non-canonical assembly routes and the generation of non-canonical HLA-B conformers has consequences for immune receptor interactions and disease therapies.
主要组织相容性复合体 I (MHC-I) 复合物在先天和适应性免疫中发挥作用,介导对细胞内环境的监测。在人类中,MHC-I 重链由三个基因编码:人类白细胞抗原 (HLA)-A、HLA-B 和 HLA-C。这些基因高度多态性,导致通常在细胞表面表达六种不同的 HLA-I 蛋白,并将多样化的肽抗原呈递给 CD8 T 细胞,以广泛监测多种致病情况。最近对 HLA-B 同种异型的研究表明,这些多态性毫不奇怪地也显著影响蛋白质折叠和组装途径。非典型组装途径的使用和非典型 HLA-B 构象的产生会对免疫受体相互作用和疾病治疗产生影响。