Laboratory of Virology, Rocky Mountain Laboratories, National Institutes of Health, Hamilton, Montana.
Rocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana.
J Infect Dis. 2023 Nov 13;228(Suppl 7):S721-S729. doi: 10.1093/infdis/jiad280.
Vesicular stomatitis virus-Ebola virus (VSV-EBOV) vaccine has been successfully used in ring vaccination approaches during EBOV disease outbreaks demonstrating its general benefit in short-term prophylactic vaccination, but actual proof of its benefit in true postexposure prophylaxis (PEP) for humans is missing. Animal studies have indicated PEP efficacy when VSV-EBOV was used within hours of lethal EBOV challenge. Here, we used a lower EBOV challenge dose and a combined intravenous and intramuscular VSV-EBOV administration to improve PEP efficacy in the rhesus macaque model. VSV-EBOV treatment 1 hour after EBOV challenge resulted in delayed disease progression but little benefit in outcome. Thus, we could not confirm previous results indicating questionable benefit of VSV-EBOV for EBOV PEP in a nonhuman primate model.
水疱性口炎病毒-埃博拉病毒(VSV-EBOV)疫苗已成功用于埃博拉病毒病暴发期间的环状疫苗接种方法,证明其在短期预防性疫苗接种方面具有普遍益处,但实际上缺乏其对人类真正暴露后预防(PEP)的益处的证据。动物研究表明,在致命的埃博拉病毒挑战后数小时内使用 VSV-EBOV 时,PEP 具有疗效。在这里,我们使用较低的埃博拉病毒挑战剂量和静脉内和肌肉内联合 VSV-EBOV 给药来提高恒河猴模型中的 PEP 疗效。在埃博拉病毒挑战后 1 小时进行 VSV-EBOV 治疗导致疾病进展延迟,但对结果几乎没有益处。因此,我们无法证实先前的结果,即在非人类灵长类动物模型中,VSV-EBOV 对埃博拉病毒 PEP 的益处值得怀疑。