Correlation of sample-to-cut-off ratio of anti-SARS-CoV-2 IgG antibody chemiluminescent assay with neutralization activity: a prospective multi-centric study in India

Aseem K. Tiwari, Gita Negi, Ram Mohan Jaiswal, Geet Aggarwal, Neeti Yadav, Virendra Kumar, Krishnan Kulathu
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引用次数: 4

Abstract

Background and Objectives

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.

Materials and Methods

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.

Results

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.

Conclusion

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.

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抗sars - cov -2 IgG抗体化学发光检测的样本截止比与中和活性的相关性:印度的一项前瞻性多中心研究
背景和目的关于商业血清学抗sars - cov -2 IgG抗体CLIA(化学发光免疫测定)检测结果与中和抗体之间关联的已发表数据有限。本研究的目的是将CLIA抗体检测的样本截止比(S/Co)与抑制活性联系起来,从而为将血浆标记为COVID恢复期血浆(CCP)进行治疗和评估疫苗疗效提供有价值的指导。材料和方法在三个地点收集了139份供体血清样本,这些供体血清样本之前为RT-PCR阳性,并且在采集样本前至少28天已完全恢复。分别用VITROS SARS-CoV-2 IgG化学发光法和GenScript cPass SARS-CoV-2代病毒中和试验(sVNT)试剂盒检测样品的S/Co比和百分之抑制活性。采用线性回归方程和受试者工作特征(ROC)曲线对S/Co与百分之百抑制率的比较模型进行检验。结果表明,化学发光IgG的S/Co比值与sVNT百分之抑制所描述的中和活性有很好的相关性。S/Co比值分别为4.04(低滴度)和8.19(高滴度),抑制率分别为30%和68%。结论化学发光法检测SARS-CoV-2 IgG可作为选择恢复期血浆治疗供体和评估疫苗接种效果的半定量检测方法,临界值为>8·19S/Co。
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