Division of Immunology and Pathogenesis, Department of Molecular and Cell Biology, University of California, LSA 421, Berkeley, CA 94720-3200, USA.
Cell Mol Life Sci. 2011 May;68(9):1471-9. doi: 10.1007/s00018-011-0655-0. Epub 2011 Mar 10.
Effectiveness of immune surveillance of intracellular viruses and bacteria depends upon a functioning antigen presentation pathway that allows infected cells to reveal the presence of an intracellular pathogen. The antigen presentation pathway uses virtually all endogenous polypeptides as a source to produce antigenic peptides that are eventually chaperoned to the cell surface by MHC class I molecules. Intriguingly, MHC I molecules present peptides encoded not only in the primary open reading frames but also those encoded in alternate reading frames. Here, we review recent studies on the generation of cryptic pMHC I. We focus on the immunological significance of cryptic pMHC I, and the novel translational mechanisms that allow production of these antigenic peptides from unconventional sources.
细胞内病毒和细菌的免疫监视的有效性取决于一个功能正常的抗原呈递途径,该途径使受感染的细胞能够揭示细胞内病原体的存在。抗原呈递途径使用几乎所有内源性多肽作为产生抗原肽的来源,这些肽最终由 MHC I 类分子伴侣递送到细胞表面。有趣的是,MHC I 分子不仅呈现主要开放阅读框编码的肽,而且还呈现交替阅读框编码的肽。在这里,我们回顾了关于隐匿性 pMHC I 产生的最新研究。我们专注于隐匿性 pMHC I 的免疫学意义,以及允许从非常规来源产生这些抗原肽的新翻译机制。