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使用新型 SARS-CoV-2 总抗体 ELISA 对明尼苏达州门诊患者和医护人员进行的 COVID-19 血清流行率初步测定。

Initial determination of COVID-19 seroprevalence among outpatients and healthcare workers in Minnesota using a novel SARS-CoV-2 total antibody ELISA.

机构信息

Department of Laboratory Medicine and Pathology, School of Medicine, University of Minnesota, Minneapolis MN, USA.

Department of Microbiology and Immunology, Center for Immunology, School of Medicine, University of Minnesota, Minneapolis, MN, USA.

出版信息

Clin Biochem. 2021 Apr;90:15-22. doi: 10.1016/j.clinbiochem.2021.01.010. Epub 2021 Feb 1.

Abstract

OBJECTIVES

To avoid the significant risks posed by the use of COVID-19 serology tests with supply chain constraints or poor performance characteristics, we developed an in-house SARS-CoV-2 total antibody test. Our test was compared with three commercial methods, and was used to determine COVID-19 seroprevalence among healthcare workers and outpatients in Minnesota.

METHODS

Seventy-nine plasma and serum samples from 50 patients 4-69 days after symptom onset who tested positive by a SARS-CoV-2 PCR method using a nasopharyngeal (NP) swab were used to evaluate our test's clinical performance. Seropositive samples were analyzed for IgG titers in a follow-up assay. Thirty plasma and serum from 12 patients who tested negative by a SARS-CoV-2 PCR method using a nasopharyngeal (NP) swab and 210 negative pre-pandemic serum samples were also analyzed. Among samples from patients > 14 days after symptom onset, the assay had 100% clinical sensitivity and 100% clinical specificity, 100% positive predictive value and 100% negative predictive value. Analytical specificity was 99.8%, indicating minimal cross-reactivity. A screening study was conducted to ascertain COVID-19 seroprevalence among healthcare workers and outpatients in Minnesota.

RESULTS

Analysis of serum collected between April 13 and May 21, 2020 indicated a COVID-19 seroprevalence of 2.96% among 1,282 healthcare workers and 4.46% among 2,379 outpatients.

CONCLUSIONS

Our in-house SARS-CoV-2 total antibody test can be used to conduct reliable epidemiological studies to inform public health decisions during the COVID-19 pandemic.

摘要

目的

为避免使用供应链受限或性能特征不佳的 COVID-19 血清学检测带来的重大风险,我们开发了一种内部 SARS-CoV-2 总抗体检测方法。我们的检测方法与三种商业方法进行了比较,并用于确定明尼苏达州医护人员和门诊患者的 COVID-19 血清流行率。

方法

使用鼻咽(NP)拭子对 SARS-CoV-2 PCR 方法检测呈阳性的 50 例 4-69 天发病后患者的 79 份血浆和血清样本,评估我们检测方法的临床性能。对血清阳性样本进行 IgG 滴度的后续检测。还分析了 12 例使用鼻咽(NP)拭子的 SARS-CoV-2 PCR 方法检测呈阴性的患者的 30 份血浆和血清以及 210 份阴性大流行前血清样本。在发病后超过 14 天的患者样本中,该检测方法具有 100%的临床灵敏度和 100%的临床特异性、100%的阳性预测值和 100%的阴性预测值。分析特异性为 99.8%,表明交叉反应性极小。进行了一项筛选研究,以确定明尼苏达州医护人员和门诊患者的 COVID-19 血清流行率。

结果

对 2020 年 4 月 13 日至 5 月 21 日采集的血清进行分析,结果显示 1282 名医护人员中 COVID-19 的血清流行率为 2.96%,2379 名门诊患者中为 4.46%。

结论

我们的内部 SARS-CoV-2 总抗体检测可用于进行可靠的流行病学研究,为 COVID-19 大流行期间的公共卫生决策提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b46f/7849522/3513ed47ab1d/gr1_lrg.jpg

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