Palmer P, Pallier C, Leruez-Ville M, Deplanche M, Morinet F
Unité de Virologie, Hôpital Saint-Louis, Paris, France.
Clin Diagn Lab Immunol. 1996 Mar;3(2):236-8. doi: 10.1128/cdli.3.2.236-238.1996.
Human parvovirus B19 recombinant VP1 and VP2 capsid proteins were produced by a procaryotic pGEX expression plasmid to evaluate the humoral response by immunoblot assay in 14 patients with primary infection. The same concentrations of VP1 and VP2 recombinant proteins were used. This demonstrates that VP1 immunoglobulin M detection and/or VP1 immunoglobulin G seroconversion is a reliable marker of primary infections. Consequently, detection of antibodies to B19 VP1 might be helpful for identifying patients at risk for chronic B19 infection or patients who are susceptible to viral reinfection.
人细小病毒B19重组VP1和VP2衣壳蛋白由原核pGEX表达质粒产生,以通过免疫印迹法评估14例原发性感染患者的体液反应。使用相同浓度的VP1和VP2重组蛋白。这表明VP1免疫球蛋白M检测和/或VP1免疫球蛋白G血清转化是原发性感染的可靠标志物。因此,检测针对B19 VP1的抗体可能有助于识别有慢性B19感染风险的患者或易发生病毒再感染的患者。