Münz Christian
Laboratory of Viral Immunobiology and Christopher H. Browne Center for Immunology and Immune Diseases, The Rockefeller University, New York, NY 10021, USA.
Cell Microbiol. 2006 Jun;8(6):891-8. doi: 10.1111/j.1462-5822.2006.00714.x.
CD4(+) T cells co-ordinate adaptive immunity and are required for immunological memory establishment and maintenance. They are thought to primarily recognize extracellular antigens, which are endocytosed, processed by lysosomal proteases and then presented on major histocompatibility complex (MHC) class II. However, recent studies have demonstrated that viral, tumour and autoantigens can gain access to this antigen presentation pathway from within cells by autophagy. This review will discuss the autophagic pathways that contribute to endogenous MHC class II antigen processing. Furthermore, potential characteristics of autophagy substrates, qualifying them to access these pathways, and regulation of autophagy will be considered. Finally, I will suggest how antigen presentation after autophagy might contribute to immune surveillance of infected and transformed cells.
CD4(+) T细胞协调适应性免疫,是建立和维持免疫记忆所必需的。它们被认为主要识别细胞外抗原,这些抗原被内吞,由溶酶体蛋白酶加工,然后呈递在主要组织相容性复合体(MHC)II类分子上。然而,最近的研究表明,病毒、肿瘤和自身抗原可通过自噬从细胞内进入这一抗原呈递途径。本综述将讨论有助于内源性MHC II类抗原加工的自噬途径。此外,还将考虑自噬底物的潜在特征,使其有资格进入这些途径,以及自噬的调控。最后,我将提出自噬后的抗原呈递可能如何有助于对受感染和转化细胞的免疫监视。