Mans, JanetZhi, LiRevilleza, Maria Jamela R.Smith, LeeRedwood, AlecNatarajan, KannanMargulies, David H.2009-04-032009-04-032009Mans, J, Zhi, L, Revilleza, MJR, Smith, L, Redwood, A, Natarajan, K & Margulies, DH 2009, ‘Structure and function of murine cytomegalovirus MHC-I-like molecules : how the virus turned the host defense to its advantage’, Immunologic Research, vol. 43, no. 1-3, pp. 264-279. [http://www.springerlink.com/content/120562/]0257-277X10.1007/s12026-008-8081-6http://hdl.handle.net/2263/9451The 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].enSpringer. The original publication is available at www.springerlink.comMHC recognitionNK cellsT cellsImmunoevasinsX-ray crystallographyMHC-Iv moleculesCytomegalovirusCytomegalovirus infectionsMajor histocompatibility complex (MHC)Killer cellsT cellsX-ray crystallographyKiller Cells, NaturalPostprint Article