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SARS-CoV-2 抗体进展和轻症 COVID-19 患者的中和潜力——一项比较长期的感染后研究。

SARS-CoV-2 antibody progression and neutralizing potential in mild symptomatic COVID-19 patients - a comparative long term post-infection study.

机构信息

MVZ Medizinische Labore Dessau Kassel GmbH, Dessau-Roßlau, Germany.

Institute of Molecular Medicine I, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.

出版信息

Front Immunol. 2022 Aug 17;13:915338. doi: 10.3389/fimmu.2022.915338. eCollection 2022.

DOI:10.3389/fimmu.2022.915338
PMID:36059441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9428854/
Abstract

BACKGROUND

Since December 2019, SARS-CoV-2 has been keeping the world in suspense. Rapid tests, molecular diagnosis of acute infections, and vaccination campaigns with vaccines are building blocks of strategic pandemic control worldwide. For laboratory diagnostics, the quantification of the antibody titer of convalescents and vaccinated patients is thus increasingly coming to the fore.

METHODS

Here we present an evaluation on the comparability of five serological tests on a cohort of 13 patients with mild COVID-19 disease. Also participants who were vaccinated after recovery were included in this study. All common immune methods (ELISA, CLIA, PETIA) and SARS-CoV-2 specific antigens (N-, S1- and RBD-) were specifically tracked and directly compared for up to 455 days. The titer of recovered participants was also set to the degree of symptoms during infection and the occurrence of Long-COVID. In addition, relative comparability of different serological tests, all standardized to WHO, was set in reference to the neutralizing potential of the corresponding participants.

FINDINGS

The individual immune responses over 455 days after a mild SARS-CoV-2 infection remain stable, in contrast to vaccinated participants. All sero-tests reveal comparable performance and dynamics during the study and compared well to a surrogate neutralization test.

CONCLUSION

The information presented here will help clinicians in the daily laboratory work in the selection and evaluation of different serological tests offered. The data also will support in respect of a sero-test-based neutralization cutoff.

摘要

背景

自 2019 年 12 月以来,SARS-CoV-2 一直令全世界感到不安。快速检测、急性感染的分子诊断和疫苗接种运动是全球战略大流行控制的基础。对于实验室诊断,因此越来越多地关注对恢复期和接种疫苗患者的抗体滴度进行定量。

方法

在这里,我们对 13 名轻度 COVID-19 患者的队列中的五种血清学检测进行了评估。本研究还包括从康复后接种疫苗的参与者。所有常见的免疫方法(ELISA、CLIA、PETIA)和 SARS-CoV-2 特异性抗原(N-、S1-和 RBD-)都被专门跟踪,并在长达 455 天的时间内直接进行比较。还将恢复期参与者的滴度与感染期间的症状程度和长 COVID 的发生联系起来。此外,根据相应参与者的中和潜力,将不同血清学检测的相对可比性全部标准化为世界卫生组织。

发现

与接种疫苗的参与者相比,在轻度 SARS-CoV-2 感染后 455 天内,个体免疫反应仍然稳定。所有血清学检测在研究期间均表现出可比的性能和动态,并且与替代中和检测很好地吻合。

结论

这里提供的信息将有助于临床医生在日常实验室工作中选择和评估提供的不同血清学检测。这些数据还将支持基于血清学检测的中和截止值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/c8c5cd63fa85/fimmu-13-915338-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/c78dc5ace827/fimmu-13-915338-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/fdad278299d3/fimmu-13-915338-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/a292f1ccf70e/fimmu-13-915338-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/f9741ab85427/fimmu-13-915338-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/c8c5cd63fa85/fimmu-13-915338-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/c78dc5ace827/fimmu-13-915338-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/fdad278299d3/fimmu-13-915338-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/a292f1ccf70e/fimmu-13-915338-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/f9741ab85427/fimmu-13-915338-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99b/9428854/c8c5cd63fa85/fimmu-13-915338-g005.jpg

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