Najít Technologies, Inc., Beaverton, OR, USA.
Division of Neuroscience, Oregon National Primate Research Center, Department of Molecular Microbiology and Immunology, Oregon Health & Science University, Beaverton, OR, USA.
Vaccine. 2019 Jul 9;37(30):4214-4221. doi: 10.1016/j.vaccine.2018.12.020. Epub 2018 Dec 31.
West Nile virus (WNV) is the most frequent mosquito-borne disease reported in the continental United States and although an effective veterinary vaccine exists for horses, there is still no commercial vaccine approved for human use. We have previously tested a 3% hydrogen peroxide (HO)-based WNV inactivation approach termed, HydroVax, in Phase I clinical trials and the vaccine was found to be safe and modestly immunogenic. Here, we describe an advanced, next-generation oxidation approach (HydroVax-II) for the development of inactivated vaccines that utilizes reduced concentrations of HO in combination with copper (cupric ions, Cu) complexed with the antiviral compound, methisazone (MZ). Further enhancement of this oxidative approach included the addition of a low percentage of formaldehyde, a cross-linking reagent with a different mechanism of action that, together with HO/Cu/MZ, provides a robust two-pronged approach to virus inactivation. Together, this new approach results in rapid virus inactivation while greatly improving the maintenance of WNV-specific neutralizing epitopes mapped across the three structural domains of the WNV envelope protein. In combination with more refined manufacturing techniques, this inactivation technology resulted in vaccine-mediated WNV-specific neutralizing antibody responses that were 130-fold higher than that observed using the first generation, HO-only vaccine approach and provided 100% protection against lethal WNV infection. This new approach to vaccine development represents an important area for future investigation with the potential not only for improving vaccines against WNV, but other clinically relevant viruses as well.
西尼罗河病毒(WNV)是美国大陆报告的最常见的蚊媒疾病,尽管已经有针对马的有效兽医疫苗,但仍没有获得批准用于人类的商业疫苗。我们之前已经在 I 期临床试验中测试了一种基于 3%过氧化氢(HO)的 WNV 灭活方法,称为 HydroVax,该疫苗被发现是安全且适度免疫原性的。在这里,我们描述了一种用于开发灭活疫苗的先进下一代氧化方法(HydroVax-II),该方法利用低浓度的 HO 与抗病毒化合物甲噻唑(MZ)结合的铜(铜离子,Cu)复合物。这种氧化方法的进一步增强包括添加低百分比的甲醛,这是一种具有不同作用机制的交联试剂,与 HO/Cu/MZ 一起,为病毒灭活提供了一种强大的双管齐下的方法。这种新方法可实现快速病毒灭活,同时大大提高了对 WNV 特异性中和表位的维持,这些表位跨越 WNV 包膜蛋白的三个结构域。结合更精细的制造技术,这种灭活技术导致疫苗介导的 WNV 特异性中和抗体反应比第一代仅使用 HO 的疫苗方法高 130 倍,并提供针对致命 WNV 感染的 100%保护。这种疫苗开发的新方法代表了未来研究的一个重要领域,不仅有可能改进针对 WNV 的疫苗,还有可能改进针对其他临床相关病毒的疫苗。