Tiwari Aseem K, Negi Gita, Jaiswal Ram Mohan, Aggarwal Geet, Yadav Neeti, Kumar Virendra, Kulathu Krishnan
Department of Transfusion Medicine Medanta-The Medicity Gurgaon India.
Department of Transfusion Medicine All India Institute of Medical Sciences Rishikesh Uttarakhand India.
ISBT Sci Ser. 2021 Nov;16(4):269-275. doi: 10.1111/voxs.12644. Epub 2021 Jun 28.
There are limited published data on association of results from commercial serological anti-SARS-CoV-2 IgG antibody CLIA (chemiluminescent immunoassay) assays with neutralizing antibodies. This study was undertaken with an objective to correlate sample-to-cut-off (S/Co) ratio of CLIA antibody tests with inhibition activity, which may then serve as a valuable guide for labelling plasma as COVID convalescent plasma (CCP) for therapy and assessing vaccine efficacy.
A total of 139 donor serum samples who were previously RT-PCR positive and had recovered completely from COVID-19 at least 28 days prior to collection of samples were recruited at three sites. The samples were analysed for S/Co ratio and per cent inhibition activity with VITROS SARS-CoV-2 IgG chemiluminescent assay and GenScript cPass SARS-CoV-2 Surrogate Virus Neutralization Test (sVNT) kit, respectively. Linear regression equation and receiver operating characteristic (ROC) curve were used to check the proposed model of comparing S/Co with per cent inhibition.
The results indicate very good correlation between the S/Co ratio of the chemiluminescent IgG assay and the neutralization activity depicted by per cent inhibition on sVNT assay. S/Co ratio of 4·04 (low-titre) and 8·19 (high-titre) correlated with 30% and 68% inhibition, respectively.
Chemiluminescent SARS-CoV-2 IgG assay can be used as a semi-quantitative test, with a cut-off of >8·19S/Co ratio for selecting donors for convalescent plasma therapy and assessing efficacy of vaccination.
关于商业血清学抗SARS-CoV-2 IgG抗体化学发光免疫分析(CLIA)检测结果与中和抗体之间关联的已发表数据有限。本研究旨在将CLIA抗体检测的样本/临界值(S/Co)比值与抑制活性相关联,这可为将血浆标记为用于治疗的新冠康复期血浆(CCP)以及评估疫苗效力提供有价值的指导。
在三个地点招募了总共139名供体血清样本,这些样本先前RT-PCR呈阳性,且在采集样本前至少28天已从新冠中完全康复。分别使用VITROS SARS-CoV-2 IgG化学发光分析和金斯瑞cPass SARS-CoV-2替代病毒中和试验(sVNT)试剂盒对样本进行S/Co比值和抑制活性百分比分析。使用线性回归方程和受试者工作特征(ROC)曲线来检验将S/Co与抑制百分比进行比较的提议模型。
结果表明化学发光IgG分析的S/Co比值与sVNT分析中以抑制百分比表示的中和活性之间具有非常好的相关性。S/Co比值为4.04(低滴度)和8.19(高滴度)分别与30%和68%的抑制率相关。
化学发光SARS-CoV-2 IgG分析可作为一种半定量检测,对于选择用于康复期血浆治疗的供体和评估疫苗效力,临界值为S/Co比值>8.19。