Hassan-Walker A F, Cope A V, Griffiths P D, Emery V C
Department of Virology, Royal Free Hospital School of Medicine, London, UK.
J Gen Virol. 1998 Sep;79 ( Pt 9):2113-6. doi: 10.1099/0022-1317-79-9-2113.
Multiplex RT-PCR analysis of human cytomegalovirus (HCMV) replication in human fibroblasts showed transcription of the natural killer (NK) cell decoy gene, UL18, from 72 h onwards. Transcription of glycoprotein B (gpUL55; a late gene) occurred from early time-points and peaked at 24 h post-infection. UL18 mRNA was also detected in the peripheral blood mononuclear cells of organ transplant recipients with HCMV viraemia, especially those with HCMV DNA virus loads greater than 10(5) genomes/ml whole blood. Thus, UL18 is produced via a low abundance transcript late during the infectious cycle at a time coincidental with the increased risk of NK cell lysis as a consequence of class I HLA down-regulation.
对人成纤维细胞中人类巨细胞病毒(HCMV)复制进行的多重逆转录聚合酶链反应(Multiplex RT-PCR)分析显示,自然杀伤(NK)细胞诱饵基因UL18从72小时起开始转录。糖蛋白B(gpUL55;一种晚期基因)在早期时间点开始转录,并在感染后24小时达到峰值。在患有HCMV病毒血症的器官移植受者的外周血单个核细胞中也检测到了UL18 mRNA,尤其是那些HCMV DNA病毒载量大于10⁵基因组/ml全血的受者。因此,UL18是在感染周期后期通过低丰度转录本产生的,此时正值由于I类HLA下调导致NK细胞裂解风险增加之际。