A simple point-of-care assay accurately detects anti-spike antibodies after SARS-CoV-2 vaccination

IF 1.6 Q4 INFECTIOUS DISEASES
Sarah E. Greene , Yuefang Huang , Wooseob Kim , Mariel J. Liebeskind , Vinay Chandrasekaran , Zhuoming Liu , Parakkal Deepak , Michael A. Paley , Daphne Lew , Monica Yang , Mehrdad Matloubian , Lianne S. Gensler , Mary C. Nakamura , Jane A. O'Hallaran , Rachel M. Presti , Sean P.J. Whelan , William J. Buchser , Alfred H.J. Kim , Gary J. Weil
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Abstract

Objective

Lateral flow assays (LFA) are sensitive for detecting antibodies to SARS-CoV-2 proteins within weeks after infection. This study tested samples from immunocompetent adults, and those receiving treatments for chronic inflammatory diseases (CID), before and after mRNA SARS-CoV-2 vaccination.

Methods

We compared results obtained with the COVIBLOCK Covid-19 LFA to those obtained by anti-spike (S) ELISA.

Results

The LFA detected anti-S antibodies in 29 of 29 (100%) of the immunocompetent and 110 of 126 (87.3%) of the CID participants after vaccination. Semiquantitative LFA scores were statistically significantly lower in samples from immunosuppressed participants, and were significantly correlated with anti-S antibody levels measured by ELISA.

Conclusions

This simple LFA test is a practical alternative to laboratory-based assays for detecting anti-S antibodies after infection or vaccination. This type of test may be most useful for testing people in outpatient or resource-limited settings.

Abstract Image

Abstract Image

一种简单的护理点检测方法可以准确检测接种严重急性呼吸系统综合征冠状病毒2型疫苗后的抗刺突抗体
目的侧流分析(LFA)对感染后数周内检测严重急性呼吸系统综合征冠状病毒2型蛋白抗体是敏感的。这项研究测试了具有免疫活性的成年人以及接受慢性炎症性疾病(CID)治疗的人在接种信使核糖核酸严重急性呼吸系统综合征冠状病毒2型疫苗前后的样本。方法将COVIBLOCK新冠肺炎LFA检测结果与抗尖峰(S)ELISA检测结果进行比较。结果LFA在29名免疫活性者中检测到29人(100%)的抗S抗体,在126名CID参与者中检测到110人(87.3%)的抗体。免疫抑制参与者的样本中,半定量LFA评分在统计学上显著较低,并且与ELISA测量的抗S抗体水平显著相关。结论这种简单的LFA测试是检测感染或接种疫苗后抗S抗体的实验室测试的一种实用替代方法。这种类型的测试对于在门诊或资源有限的环境中测试人员可能最有用。
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来源期刊
Journal of clinical virology plus
Journal of clinical virology plus Infectious Diseases
CiteScore
2.20
自引率
0.00%
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0
审稿时长
66 days
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