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欧洲的 SARS-CoV-2 中和抗体检测:为更好地使用恢复期血浆和比较试验数据,实现中和抗体滴度的标准化。

SARS-CoV-2 neutralising antibody testing in Europe: towards harmonisation of neutralising antibody titres for better use of convalescent plasma and comparability of trial data.

机构信息

University of Oxford, Oxford, United Kingdom.

Department of Immunopathology, Sanquin Research and Landsteiner Laboratory Academic Medical Centre, Amsterdam, Netherlands.

出版信息

Euro Surveill. 2021 Jul;26(27). doi: 10.2807/1560-7917.ES.2021.26.27.2100568.

Abstract

We compared the performance of SARS-CoV-2 neutralising antibody testing between 12 European laboratories involved in convalescent plasma trials. Raw titres differed almost 100-fold differences between laboratories when blind-testing 15 plasma samples. Calibration of titres in relation to the reference reagent and standard curve obtained by testing a dilution series reduced the inter-laboratory variability ca 10-fold. The harmonisation of neutralising antibody quantification is a vital step towards determining the protective and therapeutic levels of neutralising antibodies.

摘要

我们比较了 12 家参与恢复期血浆试验的欧洲实验室之间 SARS-CoV-2 中和抗体检测的性能。在对 15 个血浆样本进行盲测时,实验室间的原始滴度差异近 100 倍。通过测试一系列稀释度来校准与参考试剂的滴度和标准曲线,将实验室间的变异性降低了约 10 倍。中和抗体定量的协调是确定中和抗体保护和治疗水平的重要步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f01/8268650/88cae40d0220/2100568-f1.jpg

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