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Major Histocompatibility Complex Class I Allele-specific Cooperative and Competitive Interactions between Immune Evasion Proteins of Cytomegalovirus

机译:巨细胞病毒免疫逃逸蛋白之间的主要组织相容性复杂的I类等位基因特异性合作和竞争相互作用。

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摘要

Cytomegaloviruses (CMVs) deploy a set of genes for interference with antigen presentation in the major histocompatibility complex (MHC) class I pathway. In murine CMV (MCMV), three genes were identified so far: m04/gp34, m06/gp48, and m152/gp40. While their function as immunoevasins was originally defined after their selective expression, this may not necessarily reflect their biological role during infection. The three immunoevasins might act synergistically, but they might also compete for their common substrate, the MHC class I complexes. To approach this question in a systematic manner, we have generated a complete set of mutant viruses with deletions of the three genes in all seven possible combinations. Surface expression of a set of MHC class I molecules specified by haplotypes H-2d (Kd, Dd, and Ld) and H-2b (Kb and Db) was the parameter for evaluation of the interference with class I trafficking. The data show the following: first, there exists no additional MCMV gene of major influence on MHC class I surface expression; second, the strength of the inhibitory effect of immunoevasins shows an allele-specific hierarchy; and third, the immunoevasins act not only synergistically but can, in certain combinations, interact antagonistically. In essence, this work highlights the importance of studying the immunosubversive mechanisms of cytomegaloviruses in the context of gene expression during the viral replicative cycle in infected cells.
机译:巨细胞病毒(CMV)在主要的组织相容性复合体(MHC)I类途径中部署了一组干扰抗原呈递的基因。迄今为止,在鼠CMV(MCMV)中,已鉴定出三个基因:m04 / gp34,m06 / gp48和m152 / gp40。虽然它们的功能是在选择表达后最初确定其作为免疫evasins的功能,但这不一定反映其在感染过程中的生物学作用。这三种免疫evasins可能具有协同作用,但它们也可能竞争其共同底物MHC I类复合物。为了以系统的方式解决这个问题,我们生成了一套完整的突变病毒,其中所有七个可能的组合中的三个基因都缺失了。由单倍型H-2d(Kd,Dd和Ld)和H-2b(Kb和Db)指定的一组MHC I类分子的表面表达是评估对I类贩运的干扰的参数。数据显示:首先,不存在另外的对MHC I类表面表达有重大影响的MCMV基因。第二,免疫evasins抑制作用的强度显示等位基因特异性等级。第三,免疫evasins不仅协同作用,而且在某些组合中可以拮抗相互作用。从本质上讲,这项工作强调了在感染细胞的病毒复制周期中,在基因表达的背景下研究巨细胞病毒的免疫破坏机制的重要性。

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