Ottawa Hospital Research Institute; Department of Biochemistry, Microbiology and Immunology, University of Ottawa.
Ottawa Hospital Research Institute.
J Vis Exp. 2021 Jun 5(172). doi: 10.3791/62486.
As the COVID-19 pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to evolve, it has become evident that the presence of neutralizing antibodies against the virus may provide protection against future infection. Thus, as the creation and translation of effective COVID-19 vaccines continues at an unprecedented speed, the development of fast and effective methods to measure neutralizing antibodies against SARS-CoV-2 will become increasingly important to determine long-term protection against infection for both previously infected and immunized individuals. This paper describes a high-throughput protocol using vesicular stomatitis virus (VSV) pseudotyped with the SARS-CoV-2 spike protein to measure the presence of neutralizing antibodies in convalescent serum from patients who have recently recovered from COVID-19. The use of a replicating pseudotyped virus eliminates the necessity for a containment level 3 facility required for SARS-CoV-2 handling, making this protocol accessible to virtually any containment level 2 lab. The use of a 96-well format allows for many samples to be run at the same time with a short turnaround time of 24 h.
随着由严重急性呼吸系统综合症冠状病毒 2 型(SARS-CoV-2)引起的 COVID-19 大流行不断演变,很明显,针对该病毒的中和抗体的存在可能提供针对未来感染的保护。因此,随着针对 COVID-19 的有效疫苗的研发和翻译以空前的速度进行,开发快速有效的方法来测量针对 SARS-CoV-2 的中和抗体对于以前感染和免疫的个体来说,对确定对感染的长期保护将变得越来越重要。本文描述了一种使用带有 SARS-CoV-2 刺突蛋白的水疱性口炎病毒(VSV)假型化来测量最近从 COVID-19 中康复的患者恢复期血清中中和抗体存在的高通量方案。使用复制型假型病毒消除了处理 SARS-CoV-2 所需的 3 级生物安全实验室的必要性,使得该方案几乎可以在任何 2 级生物安全实验室进行。使用 96 孔格式可以同时运行多个样本,周转时间短至 24 小时。