一种重组 VSV 载体疫苗能迅速保护非人灵长类动物免受尼帕病毒病的致命侵害。
A recombinant VSV-vectored vaccine rapidly protects nonhuman primates against lethal Nipah virus disease.
机构信息
Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.
Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555-0610.
出版信息
Proc Natl Acad Sci U S A. 2022 Mar 22;119(12):e2200065119. doi: 10.1073/pnas.2200065119. Epub 2022 Mar 14.
SignificanceConcern has increased about the pandemic potential of Nipah virus (NiV). Similar to SARS-CoV-2, NiV is an RNA virus that is transmitted by respiratory droplets. There are currently no NiV vaccines licensed for human use. While several preventive vaccines have shown promise in protecting animals against lethal NiV disease, most studies have assessed protection 1 mo after vaccination. However, in order to contain and control outbreaks, vaccines that can rapidly confer protection in days rather than months are needed. Here, we show that a recombinant vesicular stomatitis virus vector expressing the NiV glycoprotein can completely protect monkeys vaccinated 7 d prior to NiV exposure and 67% of animals vaccinated 3 d before NiV challenge.
意义人们越来越担心尼帕病毒(NiV)的大流行潜力。与 SARS-CoV-2 类似,NiV 是一种通过呼吸道飞沫传播的 RNA 病毒。目前尚无获准用于人类的 NiV 疫苗。虽然有几种预防疫苗已显示出在保护动物免受致命 NiV 疾病方面的前景,但大多数研究都是在接种疫苗后 1 个月评估保护效果。然而,为了控制和控制疫情,需要能够在数天而不是数月内迅速提供保护的疫苗。在这里,我们表明,表达 NiV 糖蛋白的重组水疱性口炎病毒载体可以完全保护在 NiV 暴露前 7 天接种疫苗的猴子,并且 67%的动物在 NiV 攻击前 3 天接种疫苗。