Hewitt Eric W
School of Biochemistry and Molecular Biology, University of Leeds, Leeds, UK.
Immunology. 2003 Oct;110(2):163-9. doi: 10.1046/j.1365-2567.2003.01738.x.
Presumably because of the selective pressure exerted by the immune system, many viruses have evolved proteins that interfere with antigen presentation by major histocompatibility complex (MHC) class I molecules. These viruses utilize a whole variety of ingenious strategies to inhibit the MHC class I pathway. Viral proteins have been characterized that exploit bottlenecks in the MHC class I pathway, such as peptide translocation by the transporter associated with antigen processing. Alternatively, viral proteins can cause the degradation or mislocalization of MHC class I molecules. This is often achieved by the subversion of the host cell's own protein degradation and trafficking pathways. As a consequence elucidation of how these viral proteins act to subvert host cell function will continue to give important insights not only into virus-host interactions but also the function and mechanism of cellular pathways.
据推测,由于免疫系统施加的选择压力,许多病毒已经进化出能够干扰主要组织相容性复合体(MHC)I类分子抗原呈递的蛋白质。这些病毒利用各种各样巧妙的策略来抑制MHC I类途径。已经鉴定出一些病毒蛋白,它们利用MHC I类途径中的瓶颈,例如与抗原加工相关的转运体进行肽转运。另外,病毒蛋白可导致MHC I类分子的降解或定位错误。这通常是通过颠覆宿主细胞自身的蛋白质降解和运输途径来实现的。因此,阐明这些病毒蛋白如何发挥作用以颠覆宿主细胞功能,不仅将为病毒与宿主的相互作用,而且还将为细胞途径的功能和机制提供重要的见解。