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Structure and function of murine cytomegalovirus MHC-I-like molecules : how the virus turned the host defense to its advantage

机译:小鼠巨细胞病毒mHC-I样分子的结构和功能:病毒如何将宿主防御转化为其优势

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摘要

The mouse cytomegalovirus (CMV), a β-herpesvirus, exploits its large (~230 kb) double-stranded DNA genome for both essential and non-essential functions. Among the non-essential functions are those that offer the virus a selective advantage in eluding both the innate and adaptive immune responses of the host. Several non-essential genes of MCMV are thought to encode MHC-I-like genes and to function as immunoevasins. To understand further the evolution and function of these viral MHC-I (MHC-Iv) molecules, X-ray structures of several of them have been determined, not only confirming the overall MHC-I-like structure, but also elucidating features unique to this family. Future efforts promise to clarify the nature of the molecular ligands of these molecules, their evolution in the context of the adapting immune response of the murine host, and by analogy the evolution of the host response to human CMV as well. This review is based in part on a Doctoral Dissertation submitted to the Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa, for the degree of Doctor of Philosophy by Janet Mans [1].
机译:小鼠巨细胞病毒(CMV)是一种β疱疹病毒,它利用其大的(〜230 kb)双链DNA基因组来实现基本功能和非必需功能。在那些非必需功能中,有一些功能为病毒提供了选择性优势,从而可以消除宿主的先天和适应性免疫应答。人们认为,MCMV的几个非必需基因可编码MHC-1样基因,并起免疫evasins的作用。为了进一步了解这些病毒MHC-I(MHC-Iv)分子的进化和功能,已经确定了其中几个分子的X射线结构,不仅证实了整体MHC-I样结构,而且阐明了这个家庭。未来的努力有望澄清这些分子的分子配体的性质,它们在鼠宿主适应性免疫应答的情况下的进化,以及通过类推宿主对人CMV的进化。这篇评论部分基于提交给南非约翰内斯堡威特沃特斯兰德大学健康科学学院的博士学位论文,由珍妮特·芒斯(Janet Mans)授予哲学博士学位[1]。

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