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快速定量检测 SARS-CoV-2 特异性 IgG 用于评估恢复期血清。

Rapid and quantitative detection of SARS-CoV-2 specific IgG for convalescent serum evaluation.

机构信息

Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.

Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ, 07110, USA.

出版信息

Biosens Bioelectron. 2020 Dec 1;169:112572. doi: 10.1016/j.bios.2020.112572. Epub 2020 Sep 3.

Abstract

Convalescent serum with a high abundance of neutralization IgG is a promising therapeutic agent for rescuing COVID-19 patients in the critical stage. Knowing the concentration of SARS-CoV-2 S1-specific IgG is crucial in selecting appropriate convalescent serum donors. Here, we present a portable microfluidic ELISA technology for rapid (15 min), quantitative, and sensitive detection of anti-SARS-CoV-2 S1 IgG in human serum with only 8 μL sample volume. We first identified a humanized monoclonal IgG that has a high binding affinity and a relatively high specificity towards SARS-CoV-2 S1 protein, which can subsequently serve as the calibration standard of anti-SARS-CoV-2 S1 IgG in serological analyses. We then measured the abundance of anti-SARS-CoV-2 S1 IgG in 16 convalescent COVID-19 patients. Due to the availability of the calibration standard and the large dynamic range of our assay, we were able to identify "qualified donors" for convalescent serum therapy with only one fixed dilution factor (200 ×). Finally, we demonstrated that our technology can sensitively detect SARS-CoV-2 antigens (S1 and N proteins) with pg/mL level sensitivities in 40 min. Overall, our technology can greatly facilitate rapid, sensitive, and quantitative analysis of COVID-19 related markers for therapeutic, diagnostic, epidemiologic, and prognostic purposes.

摘要

恢复期富含高丰度中和 IgG 的血清是挽救 COVID-19 重症患者的有前途的治疗剂。了解 SARS-CoV-2 S1 特异性 IgG 的浓度对于选择合适的恢复期血清供体至关重要。在这里,我们提出了一种便携式微流控 ELISA 技术,可快速(15 分钟)、定量和灵敏地检测人血清中的抗 SARS-CoV-2 S1 IgG,仅需 8 μL 样品量。我们首先鉴定了一种对 SARS-CoV-2 S1 蛋白具有高结合亲和力和相对高特异性的人源化单克隆 IgG,随后可将其作为血清学分析中抗 SARS-CoV-2 S1 IgG 的校准标准。然后,我们测量了 16 名 COVID-19 恢复期患者中抗 SARS-CoV-2 S1 IgG 的丰度。由于校准标准的可用性和我们测定法的大动态范围,我们仅使用一个固定的稀释因子(200×)就能够确定恢复期血清治疗的“合格供体”。最后,我们证明我们的技术可以在 40 分钟内以 pg/mL 级别的灵敏度灵敏地检测 SARS-CoV-2 抗原(S1 和 N 蛋白)。总体而言,我们的技术可以极大地促进 COVID-19 相关标志物的快速、灵敏和定量分析,用于治疗、诊断、流行病学和预后目的。

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