Division of HIV/AIDS and Sex-transmitted Virus Vaccines, Institute for Biological Product Control, National Institutes for Food and Drug Control (NIFDC) and WHO Collaborating Center for Standardization and Evaluation of Biologicals, Beijing, China.
Graduate School of Peking Union Medical College, Beijing, China.
Nat Protoc. 2020 Nov;15(11):3699-3715. doi: 10.1038/s41596-020-0394-5. Epub 2020 Sep 25.
Pseudotyped viruses are useful virological tools because of their safety and versatility. On the basis of a vesicular stomatitis virus (VSV) pseudotyped virus production system, we developed a pseudotyped virus-based neutralization assay against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in biosafety level 2 facilities. Compared with the binding antibody test, the neutralization assay could discriminate the protective agents from the antibody family. This protocol includes production and titration of the SARS-CoV-2 S pseudotyped virus and the neutralization assay based on it. Various types of samples targeting virus attachment and entry could be evaluated for their potency, including serum samples derived from animals and humans, monoclonal antibodies and fusion inhibitors (peptides or small molecules). If the pseudotyped virus stock has been prepared in advance, it will take 2 days to get the potency data for the candidate samples. Experience in handling cells is needed before implementing this protocol.
假型病毒是一种安全且用途广泛的病毒学工具。本研究基于水疱性口炎病毒(VSV)假型病毒生产系统,在生物安全 2 级设施中开发了一种针对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的假型病毒中和测定法。与结合抗体检测相比,中和检测可将保护剂与抗体家族区分开来。本方案包括 SARS-CoV-2 S 假型病毒的生产和滴定,以及基于该病毒的中和测定。针对病毒附着和进入的各种类型的样本可评估其效力,包括来自动物和人类的血清样本、单克隆抗体和融合抑制剂(肽或小分子)。如果预先制备了假型病毒储备,则需要 2 天时间才能获得候选样本的效力数据。在实施本方案之前,需要有细胞操作经验。