Lindkvist Marie, Lahti Katarina, Lilliehöök Bo, Holmström Anna, Ahlm Clas, Bucht Göran
Department of Medical Countermeasures, Division of NBC Defence, Swedish Defence Research Agency, SE-901 82 Umeå, Sweden.
Vaccine. 2007 Feb 19;25(9):1690-9. doi: 10.1016/j.vaccine.2006.09.082. Epub 2006 Oct 11.
Hantaviruses cause hemorrhagic fever with renal syndrome (HFRS) in about 150,000 individuals in Eurasia, and several hundred cases of hantavirus pulmonary syndrome (HPS) on the American continent annually. There is consequently a need for rapid diagnostics and effective prevention of hantaviral infections. In this study we have performed DNA-vaccination of mice with full-length genes encoding the immunogenic nucleocapsid protein (NP) of Puumala (PUUV), Seoul (SEOV) and Sin Nombre virus (SNV). The antibody reactivity towards the NPs, and deleted or truncated variants thereof, were studied to localise and investigate the major polyclonal B-cell epitopes. Our findings clearly show that the antibody reactivity in each immunised mouse is unique, not only in a quantitative respect (titers) but also in cross-reactivity and most likely also in the epitope specificity. Our experimental data in combination with B-cell prediction software indicate that strong homologous virus species specific and cross-reactive epitopes are located around amino acid residue 40 in the nucleocapsid proteins.
汉坦病毒在欧亚大陆每年导致约15万人感染肾综合征出血热(HFRS),在美洲大陆每年导致数百例汉坦病毒肺综合征(HPS)。因此,迫切需要快速诊断和有效预防汉坦病毒感染。在本研究中,我们用编码普马拉病毒(PUUV)、汉城病毒(SEOV)和辛诺柏病毒(SNV)免疫原性核衣壳蛋白(NP)的全长基因对小鼠进行了DNA疫苗接种。研究了针对NP及其缺失或截短变体的抗体反应性,以定位和研究主要的多克隆B细胞表位。我们的研究结果清楚地表明,每只免疫小鼠的抗体反应性都是独特的,不仅在定量方面(滴度),而且在交叉反应性方面,很可能在表位特异性方面也是如此。我们的实验数据与B细胞预测软件相结合表明,强同源病毒种属特异性和交叉反应性表位位于核衣壳蛋白中氨基酸残基40左右。