Department of Pathology, Yale University School of Medicine, New Haven, Connecticut, USA.
J Virol. 2013 Jan;87(1):395-402. doi: 10.1128/JVI.01860-12. Epub 2012 Oct 17.
While a large number of mosquito-transmitted alphaviruses are known to cause serious human diseases, there are no licensed vaccines that protect against alphavirus infections. The alphavirus chikungunya virus (CHIKV) has caused multiple recent outbreaks of chikungunya fever. This virus has the potential to cause a worldwide epidemic and has generated strong interest in development of a prophylactic CHIKV vaccine. We report here on the development of a potent experimental vaccine for CHIKV based on a chimeric vesicular stomatitis virus (VSV) expressing the entire CHIKV envelope polyprotein (E3-E2-6K-E1) in place of the VSV glycoprotein (G). These VSVΔG-CHIKV chimeras incorporated functional CHIKV glycoproteins into the viral envelope in place of VSV G. The chimeric viruses were attenuated for growth in tissue culture but could be propagated to high titers without VSV G complementation. They also generated robust neutralizing antibody and cellular immune responses to CHIKV in mice after a single dose and protected mice against CHIKV infection. VSVΔG-alphavirus chimeras could have general applicability as alphavirus vaccines.
虽然有大量的蚊媒传播的甲病毒已知会导致严重的人类疾病,但目前还没有针对甲病毒感染的许可疫苗。甲病毒中的基孔肯雅病毒(CHIKV)已经引起了多次基孔肯雅热的爆发。这种病毒有可能引发全球流行,因此人们强烈希望开发一种预防性的 CHIKV 疫苗。我们在此报告了一种基于嵌合水疱性口炎病毒(VSV)的有效的 CHIKV 实验疫苗的开发,该疫苗表达了整个 CHIKV 包膜多蛋白(E3-E2-6K-E1),取代了 VSV 糖蛋白(G)。这些 VSVΔG-CHIKV 嵌合体将功能性 CHIKV 糖蛋白掺入病毒包膜中,取代了 VSV G。嵌合病毒在组织培养中生长减弱,但无需 VSV G 互补即可大量繁殖。它们还在单次给药后在小鼠中产生针对 CHIKV 的强大中和抗体和细胞免疫应答,并保护小鼠免受 CHIKV 感染。VSVΔG-甲病毒嵌合体可能作为甲病毒疫苗具有普遍适用性。