Department of Immunopathology, Sanquin Research and Landsteiner Laboratory Academic Medical Centre, Amsterdam, Netherlands.
Transfusion Research Center, Belgian Red Cross Flanders, Ghent, Belgium.
Vox Sang. 2023 Aug;118(8):666-673. doi: 10.1111/vox.13480. Epub 2023 Jul 4.
There is a need for conversion of SARS-CoV-2 serology data from different laboratories to a harmonized international unit. We aimed to compare the performance of multiple SARS-CoV-2 antibody serology assays among 25 laboratories across 12 European countries.
To investigate this we have distributed to all participating laboratories a panel of 15 SARS-CoV-2 plasma samples and a single batch of pooled plasma calibrated to the WHO IS 20/136 standard.
All assays showed excellent discrimination between SARS-CoV-2 seronegative plasma samples and pre-vaccinated seropositive plasma samples but differed substantially in raw antibody titres. Titres could be harmonized to binding antibody units per millilitre by calibration in relation to a reference reagent.
The standardization of antibody quantification is of paramount importance to allow interpretation and comparison of serology data reported in clinical trials in order to identify donor cohorts from whom the most effective convalescent plasma can be collected.
需要将来自不同实验室的 SARS-CoV-2 血清学数据转换为协调一致的国际单位。我们旨在比较来自 12 个欧洲国家的 25 个实验室的多种 SARS-CoV-2 抗体血清学检测方法的性能。
为了进行这项研究,我们向所有参与实验室分发了一组 15 份 SARS-CoV-2 血浆样本和一批与世界卫生组织 IS 20/136 标准校准的混合血浆。
所有检测方法均能极好地区分 SARS-CoV-2 血清阴性血浆样本和经疫苗接种后的血清阳性血浆样本,但原始抗体滴度差异很大。通过与参考试剂相关联的校准,可以将抗体滴度标准化为每毫升结合抗体单位。
抗体定量的标准化至关重要,以便解释和比较临床试验中报告的血清学数据,以确定可以从哪些供体群体中采集最有效的恢复期血浆。