Department of Pathology, Yale University School of Medicine, 310 Cedar St., LH 315, New Haven, CT 06520, USA.
J Virol. 2010 May;84(9):4611-8. doi: 10.1128/JVI.02637-09. Epub 2010 Feb 24.
The emergence in 1997 and continuance today of a highly lethal H5N1 avian influenza virus (AIV) causing human disease has raised concern about an impending pandemic and the need for a vaccine to prepare for such an occurrence. We previously generated an efficacious vesicular stomatitis virus (VSV)-based AIV vaccine expressing H5 hemagglutinin (HA) from the fifth genomic position of VSV (J. A. Schwartz et al., Virology 366:166-173, 2007). Here we have generated and characterized VSV-based vaccines that express the A/Hong Kong/156/1997 (clade 0) H5 HA from the first position of the VSV genome. These vectors induce broadly cross-neutralizing antibodies against homologous and heterologous H5N1 viruses of different clades in mice. The vaccines provide complete protection against morbidity and mortality after heterologous challenge with clade 0 and clade 1 strains in animals even 1 year after vaccination. Postchallenge pulmonary virus loads show that these vectors provide sterilizing immunity. Therefore, VSV-based AIV vaccines are potent, broadly cross-protective pandemic vaccine candidates.
1997 年出现并持续至今的高致死性 H5N1 禽流感病毒(AIV)导致人类患病,这引发了人们对即将到来的大流行的担忧,也需要一种疫苗来为此类情况做好准备。我们之前生成了一种有效的基于水疱性口炎病毒(VSV)的 AIV 疫苗,该疫苗在 VSV 的第五个基因组位置表达 H5 血凝素(HA)(J. A. Schwartz 等人,《病毒学》366:166-173, 2007)。在这里,我们生成并表征了基于 VSV 的疫苗,这些疫苗在 VSV 基因组的第一个位置表达 A/Hong Kong/156/1997(0 谱系)H5 HA。这些载体在小鼠中诱导针对同源和异源 H5N1 病毒的广泛交叉中和抗体,不同谱系。疫苗在接种后 1 年,即使在接种后 1 年,也能为动物提供针对 0 谱系和 1 谱系菌株的异源挑战的发病率和死亡率的完全保护。接种后肺部病毒载量表明,这些载体提供了杀菌免疫。因此,基于 VSV 的 AIV 疫苗是有效的、广泛交叉保护的大流行疫苗候选物。