Schmid Dorothee, Münz Christian
Laboratory of Viral Immunobiology and Christopher H. Browne Center for Immunology and Immune Diseases, The Rockefeller University, New York, New York 10021, USA.
Autophagy. 2007 Mar-Apr;3(2):133-5. doi: 10.4161/auto.3591. Epub 2007 Apr 9.
The adaptive immune system is orchestrated by CD4+ T cells. These cells detect peptides presented on Major Histocompatibility Complex (MHC) class II molecules, which are loaded in late endosomes with products of lysosomal proteolysis. One pathway by which proteins gain access to degradation in lysosomes is macroautophagy. We recently showed that constitutive macroautophagy can be detected in cells relevant for the immune system, including dendritic cells. In these antigen presenting cells, autophagosomes frequently fused with MHC class II antigen loading compartments and targeting of Influenza matrix protein 1 (MP1) for macroautophagy enhanced MHC class II presentation to MP1-specific CD4+ T cell clones up to 20 fold. Our findings indicate that macroautophagy is a constitutive and efficient pathway of antigen delivery for MHC class II presentation. We suggest that this pathway samples intracellular proteins for immune surveillance and induction of tolerance in CD4+ T cells, and could be targeted for improved MHC class II presentation of vaccine antigens.
适应性免疫系统由CD4 + T细胞协调。这些细胞检测呈递在主要组织相容性复合体(MHC)II类分子上的肽,这些肽在晚期内体中与溶酶体蛋白水解产物一起装载。蛋白质进入溶酶体进行降解的一条途径是巨自噬。我们最近发现,在包括树突状细胞在内的与免疫系统相关的细胞中可以检测到组成型巨自噬。在这些抗原呈递细胞中,自噬体经常与MHC II类抗原装载区室融合,并且将流感病毒基质蛋白1(MP1)靶向巨自噬可使MHC II类向MP1特异性CD4 + T细胞克隆的呈递增强多达20倍。我们的研究结果表明,巨自噬是MHC II类呈递的一种组成型且有效的抗原递呈途径。我们认为,该途径可对细胞内蛋白质进行采样,以用于免疫监视和诱导CD4 + T细胞的耐受性,并且可以作为改善疫苗抗原的MHC II类呈递的靶点。