Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA;
Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA.
J Immunol. 2021 Jul 1;207(1):344-351. doi: 10.4049/jimmunol.2100155. Epub 2021 Jun 28.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike pseudotyped virus (PSV) assays are widely used to measure neutralization titers of sera and of isolated neutralizing Abs (nAbs). PSV neutralization assays are safer than live virus neutralization assays and do not require access to biosafety level 3 laboratories. However, many PSV assays are nevertheless somewhat challenging and require at least 2 d to carry out. In this study, we report a rapid (<30 min), sensitive, cell-free, off-the-shelf, and accurate assay for receptor binding domain nAb detection. Our proximity-based luciferase assay takes advantage of the fact that the most potent SARS-CoV-2 nAbs function by blocking the binding between SARS-CoV-2 and angiotensin-converting enzyme 2. The method was validated using isolated nAbs and sera from spike-immunized animals and patients with coronavirus disease 2019. The method was particularly useful in patients with HIV taking antiretroviral therapies that interfere with the conventional PSV assay. The method provides a cost-effective and point-of-care alternative to evaluate the potency and breadth of the predominant SARS-CoV-2 nAbs elicited by infection or vaccines.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突假型病毒(PSV)检测广泛用于测量血清和分离的中和抗体(nAbs)的中和效价。PSV 中和检测比活病毒中和检测更安全,且不需要进入生物安全 3 级实验室。然而,许多 PSV 检测仍然具有一定的挑战性,至少需要 2 天才能完成。在这项研究中,我们报告了一种快速(<30 分钟)、灵敏、无细胞、即用型、准确的受体结合域 nAb 检测方法。我们的基于邻近的荧光素酶检测法利用了这样一个事实,即最有效的 SARS-CoV-2 nAbs 通过阻止 SARS-CoV-2 与血管紧张素转换酶 2 之间的结合来发挥作用。该方法使用分离的 nAbs 和来自接种刺突蛋白的动物和 2019 年冠状病毒病患者的血清进行了验证。该方法对于正在接受干扰常规 PSV 检测的抗逆转录病毒疗法的 HIV 患者尤其有用。该方法为评估感染或疫苗引起的主要 SARS-CoV-2 nAbs 的效力和广度提供了一种具有成本效益且便于现场使用的替代方法。