Loenen W A, Bruggeman C A, Wiertz E J
Department of Medical Microbiology, University of Maastricht, 6202 AZ Maastricht, PO BOX 5800, The Netherlands.
Semin Immunol. 2001 Feb;13(1):41-9. doi: 10.1006/smim.2001.0294.
The human cytomegalovirus (HCMV) has dedicated a significant part of its genome to genes encoding molecules that modulate the host immune response. Many of these genes have homologues in the host genome. Others, however, are unique in the sense that no obvious primary sequence identity is found in the available databases. The HCMV gene products interfere with the activation of MHC class I and class II restricted T cells and NK cells, modify the function of cytokines and their receptors, interact with complement factors and modulate signal transduction and transcription factor activity, in addition to interference with many other cellular functions. Investigation of these evasion strategies has not only improved our understanding of HCMV pathogenesis, but has also provided unexpected, novel insights into basic cell biological and immunological processes.
人类巨细胞病毒(HCMV)已将其基因组的很大一部分用于编码调节宿主免疫反应的分子的基因。这些基因中的许多在宿主基因组中有同源物。然而,其他一些基因是独特的,因为在现有数据库中未发现明显的一级序列同一性。除了干扰许多其他细胞功能外,HCMV基因产物还会干扰MHC I类和II类限制性T细胞以及NK细胞的激活,改变细胞因子及其受体的功能,与补体因子相互作用,并调节信号转导和转录因子活性。对这些逃避策略的研究不仅提高了我们对HCMV发病机制的理解,还为基本细胞生物学和免疫学过程提供了意想不到的新见解。