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一种快速高效的中和抗体筛选系统及其在 SARS-CoV-2 中的应用。

A Rapid and Efficient Screening System for Neutralizing Antibodies and Its Application for SARS-CoV-2.

机构信息

Department of Immunology, College of Basic Medicine, Chongqing Medical University, Chongqing, China.

Chongqing Key Laboratory of Basic and Translational Research of Tumor Immunology, Chongqing Medical University, Chongqing, China.

出版信息

Front Immunol. 2021 Mar 22;12:653189. doi: 10.3389/fimmu.2021.653189. eCollection 2021.

Abstract

After the pandemic of COVID-19, neutralizing antibodies (NAbs) against SARS-CoV-2 have been developed for the prophylactic and therapeutic purposes. However, few methodologies are described in detail on how to rapidly and efficiently generate effective NAbs to SARS-CoV-2. Here, we integrated and optimized a strategically screening method for NAbs, which has enabled us to obtain SARS-CoV-2 receptor-binding domain (RBD) specific NAbs within 6 days, followed by additional 9 days for antibody production and function analysis. Using this method, we obtained 198 specific Abs against SARS-CoV-2 RBD from the blood samples of COVID-19 convalescent patients, and 96 of them showed neutralizing activity. At least 20% of these NAbs exhibited advanced neutralizing potency and high affinity, with the top two NAbs showing half-maximal inhibitory concentration (IC) to block authentic SARS-CoV-2 at 9.88 and 11.13 ng/ml, respectively. Altogether, our study provides an effective methodology with high applicable value for discovering potential preventative and therapeutic NAbs for the emerging infectious diseases.

摘要

在 COVID-19 大流行之后,已经开发出针对 SARS-CoV-2 的中和抗体 (NAb) 用于预防和治疗目的。然而,很少有详细描述如何快速有效地产生针对 SARS-CoV-2 的有效 NAb 的方法。在这里,我们整合并优化了一种针对 NAb 的策略性筛选方法,使我们能够在 6 天内获得 SARS-CoV-2 受体结合域 (RBD) 特异性 NAb,然后再用 9 天进行抗体生产和功能分析。使用这种方法,我们从 COVID-19 康复患者的血液样本中获得了 198 种针对 SARS-CoV-2 RBD 的特异性 Abs,其中 96 种具有中和活性。这些 NAb 中至少有 20% 表现出先进的中和效力和高亲和力,其中前两种 NAb 阻断真实 SARS-CoV-2 的半数最大抑制浓度 (IC) 分别为 9.88 和 11.13ng/ml。总之,我们的研究为发现针对新发传染病的潜在预防和治疗性 NAb 提供了一种有效且具有高应用价值的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25b1/8019923/b680b4845413/fimmu-12-653189-g001.jpg

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