US Food and Drug Administration, Office of Vaccine Research and Review, Center for Biologics Evaluation and Research and Review, Silver Spring, Maryland, United States of America.
US Food and Drug Administration, Office of Blood Research and Review, Center for Biologics Evaluation and Research and Review, Silver Spring, Maryland, United States of America.
PLoS One. 2021 Mar 10;16(3):e0248348. doi: 10.1371/journal.pone.0248348. eCollection 2021.
Pseudoviruses are useful surrogates for highly pathogenic viruses because of their safety, genetic stability, and scalability for screening assays. Many different pseudovirus platforms exist, each with different advantages and limitations. Here we report our efforts to optimize and characterize an HIV-based lentiviral pseudovirus assay for screening neutralizing antibodies for SARS-CoV-2 using a stable 293T cell line expressing human angiotensin converting enzyme 2 (ACE2) and transmembrane serine protease 2 (TMPRSS2). We assessed different target cells, established conditions that generate readouts over at least a two-log range, and confirmed consistent neutralization titers over a range of pseudovirus input. Using reference sera and plasma panels, we evaluated assay precision and showed that our neutralization titers correlate well with results reported in other assays. Overall, our lentiviral assay is relatively simple, scalable, and suitable for a variety of SARS-CoV-2 entry and neutralization screening assays.
假病毒由于其安全性、遗传稳定性和用于筛选测定的可扩展性,是高致病性病毒的有用替代品。存在许多不同的假病毒平台,每个平台都有不同的优点和局限性。在这里,我们报告了我们优化和表征基于 HIV 的慢病毒假病毒测定法的努力,该方法使用表达人血管紧张素转换酶 2 (ACE2) 和跨膜丝氨酸蛋白酶 2 (TMPRSS2) 的稳定 293T 细胞系来筛选针对 SARS-CoV-2 的中和抗体。我们评估了不同的靶细胞,建立了至少产生两个对数范围读数的条件,并确认了在假病毒输入范围内一致的中和效价。使用参考血清和血浆面板,我们评估了测定的精密度,并表明我们的中和效价与其他测定报告的结果相关性良好。总的来说,我们的慢病毒测定法相对简单、可扩展,适用于各种 SARS-CoV-2 进入和中和筛选测定。