Minematsu T, Hosoda K, Minamishima Y
Department of Microbiology, Miyazaki Medical College.
Kansenshogaku Zasshi. 1994 Oct;68(10):1278-84. doi: 10.11150/kansenshogakuzasshi1970.68.1278.
Direct immunoperoxidase technique using human monoclonal antibody (C7) against a p65 antigen of cytomegalovirus (CMV) has been utilized to detect CMV antigen-positive leukocytes in the peripheral blood (CMV antigenemia). This technique was evaluated for enumeration of CMV antigen-positive leukocytes. The parameters included stability of the reagents, reproducibility of the results and quantitativity of the detection. The horseradish peroxidase (HRR)-labeled F(ab')2 fractions of C7 antibody were found to be superior to the equivalent Fab' fractions, because the former was much more stable than the latter. Enumeration of the CMV antigen-positive leukocytes were very reproducible and quantitative. The detection limit was one CMV antigen-positive cell per 50,000 leukocytes. Thus, this technique is reliable and practical to detect the CMV antigenemia, and it will contribute to early diagnosis of CMV diseases and initiation of antiviral therapy.
利用抗巨细胞病毒(CMV)p65抗原的人单克隆抗体(C7)的直接免疫过氧化物酶技术已用于检测外周血中的CMV抗原阳性白细胞(CMV抗原血症)。对该技术进行了评估以计数CMV抗原阳性白细胞。参数包括试剂的稳定性、结果的可重复性和检测的定量性。发现辣根过氧化物酶(HRR)标记的C7抗体F(ab')2片段优于等效的Fab'片段,因为前者比后者稳定得多。CMV抗原阳性白细胞的计数具有非常好的可重复性和定量性。检测限为每50,000个白细胞中有一个CMV抗原阳性细胞。因此,该技术检测CMV抗原血症可靠且实用,将有助于CMV疾病的早期诊断和抗病毒治疗的启动。