Harper D R, Grose C
Department of Virology, Medical College of St. Bartholomew's Hospital, London, United Kingdom.
J Infect Dis. 1989 Mar;159(3):444-51. doi: 10.1093/infdis/159.3.444.
Varicella-zoster virus (VZV) directs the synthesis of a nonglycosylated polypeptide complex with two prominent species with relative molecular masses of 32,000 and 36,000; the p32/p36 complex is present in both the viral nucleocapsid and the nuclear matrix of the infected cell. We have now further characterized the humoral immune response of VZV-infected humans to this complex and established that it is a major viral antigen. Antibodies to VZV p32/p36 were detected in sera from patients with both primary VZV infection (chickenpox) and VZV reactivation (zoster); the response after zoster was more pronounced. When the IgM and IgG components of the immune response were distinguished, IgM to the viral nucleoproteins was observed following chickenpox and zoster and, to a lesser extent, in recipients of VZV vaccine. An IgM response to VZV p32 also was detected during intrauterine VZV infection and subclinical VZV infection.
水痘带状疱疹病毒(VZV)指导合成一种非糖基化多肽复合物,该复合物有两种主要成分,相对分子质量分别为32,000和36,000;p32/p36复合物存在于病毒核衣壳和受感染细胞的核基质中。我们现在进一步研究了VZV感染人类后对该复合物的体液免疫反应,并确定它是一种主要的病毒抗原。在原发性VZV感染(水痘)和VZV再激活(带状疱疹)患者的血清中均检测到了针对VZV p32/p36的抗体;带状疱疹后的反应更为明显。当区分免疫反应的IgM和IgG成分时,在水痘和带状疱疹后观察到了针对病毒核蛋白的IgM,在VZV疫苗接种者中程度较轻。在子宫内VZV感染和亚临床VZV感染期间也检测到了针对VZV p32的IgM反应。