Are anti-SARS-CoV-2 S/N IgG/IgM antibodies always predictive of previous SARS-CoV-2 infection?

IF 1.1 Q4 MEDICAL LABORATORY TECHNOLOGY
Advances in laboratory medicine Pub Date : 2023-03-24 eCollection Date: 2023-06-01 DOI:10.1515/almed-2023-0008
Giuseppe Lippi, Brandon M Henry, Laura Pighi, Simone De Nitto, Gian Luca Salvagno
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Abstract

Objectives: We planned this study to verify whether immunoassays for quantifying anti-SARS-CoV-2 IgG/IgM antibodies against both spike (S) and nucleocapsid (N) proteins may be used for identifying previous SARS-CoV-2 infections.

Methods: The study population consisted of a cohort of fully vaccinated healthcare workers. All study subjects underwent regular medical visits and molecular testing for diagnosing SARS-CoV-2 infections every 2-4 weeks between 2020-2022. Venous blood was drawn for measuring anti-SARS-CoV-2 antibodies with MAGLUMI 2019-nCoV lgG/IgM CLIA Assays directed against both SARS-CoV-2 S and N proteins.

Results: Overall, 31/53 (58.5%) subjects had tested positive for SARS-CoV-2 by RT-PCR throughout the study (24 once, 7 twice). No positive correlation was found between anti-SARS-CoV-2 S/N IgM antibodies and molecular test positivity. In univariate regression analysis, both a molecular test positivity (r=0.33; p=0.015) and the number of positive molecular tests (r=0.43; p=0.001), but not vaccine doses (r=-0.12; p=0.392), were significantly correlated with anti-SARS-CoV-2 S/N IgG antibodies. These two associations remained significant in multiple linear regression analysis (p=0.029 and p<0.001, respectively) after adjusting for sex, age, body mass index, and vaccine doses. In ROC curve analysis, anti-SARS-CoV-2 S/N IgG antibodies significantly predicted molecular test positivity (AUC, 0.69; 95% CI; 0.55-0.84), with the best cutoff of 0.05 AU/mL displaying 67.9% accuracy, 0.97 sensitivity, and 0.27 specificity.

Conclusions: Although anti-SARS-CoV-2 S/N IgG antibodies provide helpful information for identifying previous SARS-CoV-2 infections, a lower cutoff than that of sample reactivity should be used. Anti-SARS-CoV-2 S/N IgM antibodies using conventional cutoffs seem useless for this purpose.

抗SARS-CoV-2 S/N IgG/IgM抗体是否总是预测先前的SARS-CoV-2感染?
摘要目的我们计划进行这项研究,以验证用于量化针对刺突蛋白(S)和核衣壳蛋白(N)的抗严重急性呼吸系统综合征冠状病毒2型IgG/IgM抗体的免疫测定是否可用于识别先前的严重急性呼吸系统冠状病毒2型感染。方法研究人群由完全接种疫苗的医护人员组成。2020-2022年间,所有研究受试者每2-4周接受一次定期医疗访问和分子检测,以诊断严重急性呼吸系统综合征冠状病毒2型感染。用针对严重急性呼吸系统综合征冠状病毒2型S和N蛋白的MAGLUMI 2019-nCoV lgG/IgM CLIA测定法抽取静脉血以测量抗严重急性呼吸系冠状病毒2型抗体。结果总体而言,在整个研究过程中,31/53(58.5%)的受试者通过RT-PCR检测出严重急性呼吸系统综合征冠状病毒2型呈阳性(24次,7次)。抗严重急性呼吸系统综合征冠状病毒2型S/N IgM抗体与分子检测阳性之间没有发现正相关性。在单变量回归分析中,分子检测阳性率(r=0.33;p=0.015)和阳性分子检测次数(r=0.43;p=0.001)与抗严重急性呼吸系统综合征冠状病毒2 S/N IgG抗体显著相关,但与疫苗剂量无关(r=−0.12;p=0.392)。在对性别、年龄、体重指数和疫苗剂量进行调整后,这两种相关性在多元线性回归分析中仍然显著(分别为p=0.029和p<0.001)。在ROC曲线分析中,抗严重急性呼吸系统综合征冠状病毒2 S/N IgG抗体显著预测分子测试阳性(AUC,0.69;95%CI;0.55–0.84),0.05 AU/mL的最佳截止值显示67.9%的准确率、0.97的敏感性和0.27的特异性。结论尽管抗严重急性呼吸系统综合征冠状病毒2型S/N IgG抗体为识别先前的严重急性呼吸系冠状病毒2型感染提供了有用的信息,但应使用低于样本反应性的截止值。使用常规切口的抗SARS-CoV-2 S/N IgM抗体似乎对此毫无用处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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