Stöckl E, Popow-Kraupp T, Heinz F X, Mühlbacher F, Balcke P, Kunz C
Institute of Virology, University of Vienna, Austria.
J Clin Microbiol. 1988 Dec;26(12):2536-40. doi: 10.1128/jcm.26.12.2536-2540.1988.
In situ hybridization with a probe specific for immediate-early genes was used for detection of cytomegalovirus (CMV) transcripts in peripheral blood mononuclear cells, and the potential use of this technique as a diagnostic tool was assessed. The results were compared with those obtained with conventional assay systems. In 8 of 18 continually observed patients who developed a productive CMV infection, a high number of hybridization-positive cells were observed 1 to 2 weeks before the conventional tests yielded positive results. Thus, quantitative evaluation of hybridization results provided an early and specific marker for beginning CMV infection or reactivation. In three cases, quantitative in situ hybridization assays provided the only laboratory marker indicating CMV infection or reactivation. It was also found that a probe specific for immediate-early genes was superior to a probe specific for late genes for diagnosis of productive infections.
使用针对即刻早期基因的特异性探针进行原位杂交,以检测外周血单个核细胞中的巨细胞病毒(CMV)转录本,并评估该技术作为诊断工具的潜在用途。将结果与使用传统检测系统获得的结果进行比较。在18例持续观察到发生活动性CMV感染的患者中,有8例在传统检测结果呈阳性前1至2周观察到大量杂交阳性细胞。因此,杂交结果的定量评估为CMV感染开始或再激活提供了早期且特异性的标志物。在3例病例中,定量原位杂交检测是表明CMV感染或再激活的唯一实验室标志物。还发现,针对即刻早期基因的特异性探针在诊断活动性感染方面优于针对晚期基因的特异性探针。