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Single Immunization With a Monovalent Vesicular Stomatitis Virus–Based Vaccine Protects Nonhuman Primates Against Heterologous Challenge With Bundibugyo ebolavirus

机译:基于单价水泡性口腔炎病毒的疫苗的单次免疫可保护非人类灵长类动物免受Bundibugyo埃博拉病毒的异源攻击

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摘要

The recombinant vesicular stomatitis virus (rVSV) vector-based monovalent vaccine platform expressing a filovirus glycoprotein has been demonstrated to provide protection from lethal challenge with Ebola (EBOV) and Marburg (MARV) viruses both prophylactically and after exposure. This platform provides protection between heterologous strains within a species; however, protection from lethal challenge between species has been largely unsuccessful. To determine whether the rVSV-EBOV vaccines have the potential to provide protection against a newly emerging, phylogenetically related species, cynomolgus macaques were vaccinated with an rVSV vaccine expressing either the glycoprotein of Zaire ebolavirus (ZEBOV) or Côte d’Ivoire ebolavirus (CIEBOV) and then challenged with Bundibugyo ebolavirus (BEBOV), which was recently proposed as a new EBOV species following an outbreak in Uganda in 2007. A single vaccination with the ZEBOV–specific vaccine provided cross-protection (75% survival) against subsequent BEBOV challenge, whereas vaccination with the CIEBOV–specific vaccine resulted in an outcome similar to mock-immunized animals (33% and 25% survival, respectively). This demonstrates that monovalent rVSV-based vaccines may be useful against a newly emerging species; however, heterologous protection across species remains challenging and may depend on enhancing the immune responses either through booster immunizations or through the inclusion of multiple immunogens.
机译:已证明表达线状病毒糖蛋白的重组水泡性口炎病毒(rVSV)载体单价疫苗平台可提供预防性和暴露后的埃博拉(EBOV)和马尔堡(MARV)病毒致命性攻击保护。该平台在物种内的异源菌株之间提供保护;但是,保护物种免受致命挑战的努力在很大程度上还没有成功。为了确定rVSV-EBOV疫苗是否有潜力针对新出现的,与系统发育相关的物种提供保护,猕猴猕猴接种了表达Zaire埃博拉病毒(ZEBOV)或科特迪瓦埃博拉病毒(CIEBOV)糖蛋白的rVSV疫苗然后用Bundibugyo埃博拉病毒(BEBOV)挑战,该病毒最近在2007年乌干达爆发后被提议作为一种新的EBOV物种。ZEBOV特异性疫苗的单次疫苗接种提供了交叉保护(75%的存活率),可抵抗随后的BEBOV挑战,而用CIEBOV特异疫苗进行疫苗接种的结果与模拟免疫动物相似(分别为33%和25%存活率)。这表明基于rVSV的单价疫苗可能对新兴物种有用。然而,跨物种的异源保护仍然具有挑战性,可能取决于通过加强免疫或通过包含多种免疫原来增强免疫反应。

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  • 来源
    《Journal of Infectious Diseases》 |2011年第3期|p.1082-1089|共8页
  • 作者单位

    Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada|Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada|Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Disease, National Institutes of Health, Hamilton, Montana;

    Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada|Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Disease, National Institutes of Health, Hamilton, Montana;

    Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada;

    Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada;

    Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada|Laboratory of Virology, Division of Int;

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