一种嵌合表达 RBD 的灭活重组狂犬病病毒诱导针对 SARS-CoV-2 和 RABV 的体液和细胞免疫。

An inactivated recombinant rabies virus chimerically expressed RBD induces humoral and cellular immunity against SARS-CoV-2 and RABV.

机构信息

Key Laboratory of Zoonosis Research, Ministry of Education, College of Veterinary Medicine, Jilin University, Changchun, 130062, China.

Key Laboratory of Zoonosis Research, Ministry of Education, College of Veterinary Medicine, Jilin University, Changchun, 130062, China; Changchun Sino Biotechnology Co., Ltd., Changchun, 130012, China.

出版信息

Virol Sin. 2023 Apr;38(2):244-256. doi: 10.1016/j.virs.2022.12.006. Epub 2022 Dec 29.

Abstract

Many studies suggest that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can infect various animals and transmit among animals, and even to humans, posing a threat to humans and animals. There is an urgent need to develop inexpensive and efficient animal vaccines to prevent and control coronavirus disease 2019 (COVID-19) in animals. Rabies virus (RABV) is another important zoonotic pathogen that infects almost all warm-blooded animals and poses a great public health threat. The present study constructed two recombinant chimeric viruses expressing the S1 and RBD proteins of the SARS-CoV-2 Wuhan01 strain based on a reverse genetic system of the RABV SRV9 strain and evaluated their immunogenicity in mice, cats and dogs. The results showed that both inactivated recombinant viruses induced durable neutralizing antibodies against SARS-CoV-2 and RABV and a strong cellular immune response in mice. Notably, inactivated SRV-nCoV-RBD induced earlier antibody production than SRV-nCoV-S1, which was maintained at high levels for longer periods. Inactivated SRV-nCoV-RBD induced neutralizing antibodies against both SARS-CoV-2 and RABV in cats and dogs, with a relatively broad-spectrum cross-neutralization capability against the SARS-CoV-2 pseudoviruses including Alpha, Beta, Gamma, Delta, and Omicron, showing potential to be used as a safe bivalent vaccine candidate against COVID-19 and rabies in animals.

摘要

许多研究表明,严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)可以感染各种动物并在动物间传播,甚至传播给人类,对人类和动物构成威胁。迫切需要开发廉价且高效的动物疫苗来预防和控制动物中的 2019 年冠状病毒病(COVID-19)。狂犬病病毒(RABV)是另一种重要的人畜共患病病原体,几乎感染所有温血动物,对公共卫生构成巨大威胁。本研究基于 RABV SRV9 株的反向遗传系统,构建了表达 SARS-CoV-2 武汉 01 株 S1 和 RBD 蛋白的两种重组嵌合病毒,并在小鼠、猫和狗中评估了它们的免疫原性。结果表明,两种灭活重组病毒均能诱导小鼠产生针对 SARS-CoV-2 和 RABV 的持久中和抗体和强烈的细胞免疫反应。值得注意的是,与 SRV-nCoV-S1 相比,灭活的 SRV-nCoV-RBD 更早地诱导了抗体产生,且维持时间更长。灭活的 SRV-nCoV-RBD 能诱导猫和狗产生针对 SARS-CoV-2 和 RABV 的中和抗体,对包括 Alpha、Beta、Gamma、Delta 和 Omicron 在内的 SARS-CoV-2 假病毒具有广谱交叉中和能力,显示出作为一种安全的二价疫苗候选物用于预防动物中的 COVID-19 和狂犬病的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3284/10176443/7cc249565641/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索