Beisser P S, Goh C S, Cohen F E, Michelson S
Unité d'Immunologie Virale, Institut Pasteur, 28 Rue du Docteur Roux, 75274 Paris, France.
Curr Top Microbiol Immunol. 2002;269:203-34. doi: 10.1007/978-3-642-59421-2_13.
The ubiquitous, opportunistic pathogen human cytomegalovirus (CMV) encodes several proteins homologous to those of the host organism. Four different CMV genes encode chemokine receptor-like peptides. These genes, UL33, UL78, US27, and US28, are expressed at various stages of infection in vitro. Their functions remain largely unknown. To date, chemokine binding and signalling has only been demonstrated for the US28 gene product. Putative ligands for the other CMV-encoded chemokine receptors are discussed on basis of phylogenetic analysis. The potential roles of these receptors in virus trafficking, persistence, and immune evasion are summarized. Similarly, modulation of expression of the host chemokines IL-8, MCP-1a and RANTES in relation to viral dissemination and persistence is reviewed.
无处不在的机会性病原体人类巨细胞病毒(CMV)编码了几种与宿主生物体蛋白质同源的蛋白质。四种不同的CMV基因编码趋化因子受体样肽。这些基因,即UL33、UL78、US27和US28,在体外感染的各个阶段都有表达。它们的功能在很大程度上仍然未知。迄今为止,仅证实了US28基因产物具有趋化因子结合和信号传导功能。基于系统发育分析讨论了其他CMV编码趋化因子受体的推定配体。总结了这些受体在病毒运输、持续存在和免疫逃逸中的潜在作用。同样,也综述了宿主趋化因子IL-8、MCP-1a和RANTES的表达调节与病毒传播和持续存在的关系。