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MHC II类分子介导的抗原加工与呈递的来龙去脉。

The ins and outs of MHC class II-mediated antigen processing and presentation.

作者信息

Roche Paul A, Furuta Kazuyuki

机构信息

Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-9760, USA.

Department of Immunobiology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama 7008530, Japan.

出版信息

Nat Rev Immunol. 2015 Apr;15(4):203-16. doi: 10.1038/nri3818. Epub 2015 Feb 27.

Abstract

Antigenic peptide-loaded MHC class II molecules (peptide-MHC class II) are constitutively expressed on the surface of professional antigen-presenting cells (APCs), including dendritic cells, B cells, macrophages and thymic epithelial cells, and are presented to antigen-specific CD4(+) T cells. The mechanisms of antigen uptake, the nature of the antigen processing compartments and the lifetime of cell surface peptide-MHC class II complexes can vary depending on the type of APC. It is likely that these differences are important for the function of each distinct APC subset in the generation of effective adaptive immune responses. In this Review, we describe our current knowledge of the mechanisms of uptake and processing of antigens, the intracellular formation of peptide-MHC class II complexes, the intracellular trafficking of peptide-MHC class II complexes to the APC plasma membrane and their ultimate degradation.

摘要

负载抗原肽的MHC II类分子(肽-MHC II类分子)在专职抗原呈递细胞(APC)表面组成性表达,专职抗原呈递细胞包括树突状细胞、B细胞、巨噬细胞和胸腺上皮细胞,并呈递给抗原特异性CD4(+) T细胞。抗原摄取机制、抗原加工区室的性质以及细胞表面肽-MHC II类复合物的寿命可能因APC的类型而异。这些差异可能对每个不同的APC亚群在产生有效的适应性免疫反应中的功能很重要。在本综述中,我们描述了我们目前对抗原摄取和加工机制、肽-MHC II类复合物的细胞内形成、肽-MHC II类复合物向APC质膜的细胞内运输及其最终降解的认识。

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