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用Sad23L-nCoV-S候选疫苗对猫进行针对严重急性呼吸综合征冠状病毒2主要变体的疫苗接种。

Vaccination of cats with Sad23L-nCoV-S vaccine candidate against major variants of SARS-CoV-2.

作者信息

Zhang Panli, Luo Shengxue, Zou Peng, Liang Chaolan, Wang Cong, Li Jinfeng, Li Yongyin, Wang Gang, Zhang Ling, Li Tingting, Li Chengyao

机构信息

Department of Transfusion Medicine, School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou 510515, China.

Department of Pediatrics, Shenzhen Hospital, Southern Medical University, Shenzhen 518101, China.

出版信息

Mol Ther Methods Clin Dev. 2022 Sep 8;26:181-190. doi: 10.1016/j.omtm.2022.06.011. Epub 2022 Jun 22.

Abstract

Cats are susceptible to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and risk transmitting viruses to naive cats or humans. Here, based on our novel adenovirus-vectored COVID-19 vaccine, the immunogenicity of Sad23L-nCoV-S vaccine was evaluated in cats by prime-boost vaccinations. Five cats were primed with a dose of 10 plaque-forming units (PFUs) Sad23L-nCoV-S vaccine and then boosted with an equal dose of same vaccine at a 4-week interval. Cat serum neutralizing antibody (NAb) titers (the sample dilution at which 50% inhibitory concentration [IC]) were measured as IC 15,849 to wild-type strain, IC 6,591 to Alpha, IC 2,315 to Beta, IC 2,744 to Gamma, IC 1,848 to Delta, and IC 318 to Omicron variants of pseudotyped SARS-CoV-2 viruses at week 6 post-prime vaccination. All NAb levels to these five variants were ≥IC 49 from vaccinated cats at week 10, while 48.8% to Delta and 100% to Omicron variants were <IC 10 from human vaccinees at week 2 or 4 after receiving two injections of the inactivated SARS-CoV-2 vaccines. Robust T cell response of interferon (IFN)-γ to S peptides were detected in vaccinated cats. It was concluded that Sad23L-nCoV-S vaccine could be a promising vaccine candidate against SARS-CoV-2 infection in cats by prime or plus boost vaccinations.

摘要

猫易感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2),并有将病毒传播给未感染猫或人类的风险。在此,基于我们新型的腺病毒载体COVID-19疫苗,通过初免-加强免疫接种对Sad23L-nCoV-S疫苗在猫中的免疫原性进行了评估。五只猫用10个空斑形成单位(PFU)的Sad23L-nCoV-S疫苗进行初免,然后在4周间隔后用相同剂量的相同疫苗进行加强免疫。在初免接种后第6周,测定猫血清中和抗体(NAb)滴度(50%抑制浓度[IC]时的样本稀释度),对野生型毒株为IC 15,849,对Alpha毒株为IC 6,591,对Beta毒株为IC 2,315,对Gamma毒株为IC 2,744,对Delta毒株为IC 1,848,对SARS-CoV-2假型病毒的Omicron变体为IC 318。在第10周时,接种疫苗的猫对这五种变体的所有NAb水平均≥IC 49,而在接受两剂灭活SARS-CoV-2疫苗后第2周或第4周,人类疫苗接种者对Delta毒株的48.8%和对Omicron变体的100%均<IC 10。在接种疫苗的猫中检测到对S肽的强大干扰素(IFN)-γ T细胞反应。得出的结论是,Sad23L-nCoV-S疫苗通过初免或加强免疫接种可能是一种有前景的抗猫SARS-CoV-2感染的候选疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/285c/9263530/92b0311db516/fx1.jpg

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