Division of HIV/AIDS and Sex-transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC), Beijing, People's Republic of China.
Graduate School of Peking Union Medical College, Beijing, People's Republic of China.
Emerg Microbes Infect. 2020 Dec;9(1):680-686. doi: 10.1080/22221751.2020.1743767.
Pseudoviruses are useful virological tools because of their safety and versatility, especially for emerging and re-emerging viruses. Due to its high pathogenicity and infectivity and the lack of effective vaccines and therapeutics, live SARS-CoV-2 has to be handled under biosafety level 3 conditions, which has hindered the development of vaccines and therapeutics. Based on a VSV pseudovirus production system, a pseudovirus-based neutralization assay has been developed for evaluating neutralizing antibodies against SARS-CoV-2 in biosafety level 2 facilities. The key parameters for this assay were optimized, including cell types, cell numbers, virus inoculum. When tested against the SARS-CoV-2 pseudovirus, SARS-CoV-2 convalescent patient sera showed high neutralizing potency, which underscore its potential as therapeutics. The limit of detection for this assay was determined as 22.1 and 43.2 for human and mouse serum samples respectively using a panel of 120 negative samples. The cutoff values were set as 30 and 50 for human and mouse serum samples, respectively. This assay showed relatively low coefficient of variations with 15.9% and 16.2% for the intra- and inter-assay analyses respectively. Taken together, we established a robust pseudovirus-based neutralization assay for SARS-CoV-2 and are glad to share pseudoviruses and related protocols with the developers of vaccines or therapeutics to fight against this lethal virus.
假病毒是一种安全且多功能的病毒学工具,尤其适用于新兴和重现的病毒。由于其高致病性和感染力,以及缺乏有效的疫苗和治疗方法,活 SARS-CoV-2 必须在生物安全 3 级条件下处理,这阻碍了疫苗和治疗方法的开发。基于 VSV 假病毒生产系统,我们开发了一种基于假病毒的中和测定法,用于在生物安全 2 级设施中评估针对 SARS-CoV-2 的中和抗体。优化了该测定法的关键参数,包括细胞类型、细胞数量、病毒接种量。当用 SARS-CoV-2 假病毒进行测试时,SARS-CoV-2 恢复期患者血清显示出高中和效力,这突出了其作为治疗方法的潜力。使用 120 个阴性样本的面板,该测定法的检测限分别为人血清和鼠血清样本的 22.1 和 43.2。人血清和鼠血清样本的截止值分别设定为 30 和 50。该测定法的内和间分析变异系数分别为 15.9%和 16.2%,相对较低。总之,我们建立了一种针对 SARS-CoV-2 的稳健的基于假病毒的中和测定法,并很高兴与疫苗或治疗方法的开发者共享假病毒和相关方案,以对抗这种致命病毒。