Früh K, Ahn K, Peterson P A
R.W. Johnson Pharmaceutical Research Institute, IMM 23, Scripps Research Institute, La Jolla, CA 92027, USA.
J Mol Med (Berl). 1997 Jan;75(1):18-27. doi: 10.1007/s001090050082.
An essential part of the immune response to viral infections is the recognition and elimination of infected cells by cytotoxic T lymphocytes. For this purpose a display mechanism has evolved which is present in almost all nucleated cells: the major histocompatibility complex class I antigen processing pathway. Both self and foreign antigens are degraded in the cytosol to peptides which are translocated into the endoplasmic reticulum where they are loaded onto MHC class I molecules. Pathogens living inside the cell are evolving under the constant selection pressure of such immune surveillance. As a result such infectious organisms have developed a variety of strategies to prevent their antigens from being presented. Since our understanding of the cell biology of antigen presentation has greatly advanced in recent years, it has now become possible to unravel several of the molecular mechanisms by which viruses interfere with MHC class I antigen presentation. Examples for the interference of viral molecules with components of the MHC class I pathway are presented in this review.
对病毒感染免疫反应的一个重要部分是细胞毒性T淋巴细胞对受感染细胞的识别和清除。为此,一种几乎存在于所有有核细胞中的展示机制得以进化:主要组织相容性复合体I类抗原加工途径。自身抗原和外来抗原在细胞质中都被降解为肽,这些肽被转运到内质网,在那里它们被加载到MHC I类分子上。生活在细胞内的病原体在这种免疫监视的持续选择压力下不断进化。因此,这类感染性生物体已经发展出多种策略来阻止其抗原被呈递。由于近年来我们对抗抗原呈递的细胞生物学的理解有了很大进展,现在已经有可能揭示病毒干扰MHC I类抗原呈递的几种分子机制。本综述介绍了病毒分子干扰MHC I类途径成分的实例。