Schoppel K, Kropff B, Schmidt C, Vornhagen R, Mach M
Institut für Klinische und Molekulare Virologie, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany.
J Infect Dis. 1997 Mar;175(3):533-44. doi: 10.1093/infdis/175.3.533.
An individual analysis of IgG antibodies against 12 known antigenic domains of human cytomegalovirus (HCMV)-derived structural phospho- and glycoproteins and nonstructural polypeptides was performed. In HCMV-seropositive healthy persons, the separate determination of antibody titers against the various antigens resulted in an antibody profile that was characteristic for each individual. Profiles were qualitatively stable over a period of >4 years. However, quantitative changes were observed in some persons. During primary HCMV infection, a delay of 50-100 days in the appearance of glycoprotein-specific antibodies was observed, whereas immunoglobulins directed against other HCMV-specific antigens were promptly synthesized. In contrast, during reactivation or reinfection, a synchronized production of antibodies was found. Levels of glycoprotein-specific antibodies and detection of viral DNA in peripheral blood inversely correlated. Precursor B cell analyses showed no significant differences between glycoprotein-specific and phosphoprotein-specific B cells.
对针对人巨细胞病毒(HCMV)衍生的结构磷蛋白和糖蛋白以及非结构多肽的12个已知抗原结构域的IgG抗体进行了个体分析。在HCMV血清阳性的健康人中,针对各种抗原单独测定抗体滴度,得到了每个人特有的抗体谱。这些谱在超过4年的时间里在质量上是稳定的。然而,在一些人中观察到了定量变化。在原发性HCMV感染期间,观察到糖蛋白特异性抗体出现延迟50 - 100天,而针对其他HCMV特异性抗原的免疫球蛋白则迅速合成。相反,在病毒再激活或再次感染期间,发现抗体同步产生。糖蛋白特异性抗体水平与外周血中病毒DNA的检测呈负相关。前体B细胞分析显示,糖蛋白特异性B细胞和磷蛋白特异性B细胞之间没有显著差异。