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一种快速 SARS-CoV-2 抗体检测试纸的研发与临床应用:中国多中心评估。

Development and clinical application of a rapid SARS-CoV-2 antibody test strip: A multi-center assessment across China.

机构信息

Health Management Center, Xiangya Hospital of Central South University, Changsha, China.

Infectious Diseases Hospital of Xuzhou City, Xuzhou, China.

出版信息

J Clin Lab Anal. 2021 Jan;35(1):e23619. doi: 10.1002/jcla.23619. Epub 2020 Oct 16.

Abstract

BACKGROUND

The ongoing coronavirus disease 19 (COVID-19) is posing a threat to the public health globally. Serological test for SARS-CoV-2 antibody can improve early diagnosis of COVID-19 and serves as a valuable supplement to RNA detection.

METHOD

A SARS-CoV-2 IgG/IgM combined antibody test strip based on colloidal gold immunochromatography assay was developed, with both spike protein and nucleocapsid protein of SARS-CoV-2 antigen used for antibody detection. From 3 medical institutions across China, serum or plasma of 170 patients with confirmed COVID-19 diagnosis and 300 normal controls were collected and tested with the strip. Sensitivity, specificity, kappa coefficient, receiver operating characteristic (ROC) curve, and area under the curve (AUC) were analyzed. Positive rates in different medical centers, age group, gender, and different disease course were compared.

RESULTS

158 out 170 samples from confirmed COVID-19 patients had positive results from the test, and 296 out of 300 samples from normal controls had negative results. The kit was 92.9% sensitive and 98.7% specific. The positive rate was 77.3% during the first week after disease onset, but reached 100% since day 9. AUC and kappa coefficient were 0.958 and 0.926, respectively, which showed the consistency of the test results with the standard diagnosis. Age or gender caused little variations in the kit sensitivity.

CONCLUSION

The rapid, easy-to-use SARS-CoV-2 IgG/IgM combined antibody test kit has a superior performance, which can help with accurate diagnosis and thus timely treatment and isolation of COVID-19 patients, that contributes to the better control of the global pandemic.

摘要

背景

当前,新型冠状病毒病 2019(COVID-19)在全球范围内对公众健康构成威胁。SARS-CoV-2 抗体血清学检测可提高 COVID-19 的早期诊断能力,是 RNA 检测的有益补充。

方法

本研究开发了一种基于胶体金免疫层析法的 SARS-CoV-2 抗体 IgG/IgM 联合检测试剂盒,用于检测 SARS-CoV-2 的棘突蛋白和核衣壳蛋白抗原。我们收集了来自中国 3 家医疗机构的 170 例确诊 COVID-19 患者的血清或血浆以及 300 例健康对照者的血清或血浆,并用该试剂盒进行检测。评估了试剂盒的灵敏度、特异性、kappa 系数、受试者工作特征(ROC)曲线和曲线下面积(AUC)。比较了不同医疗机构、年龄组、性别和不同病程患者的阳性率。

结果

在 170 例确诊 COVID-19 患者的样本中,有 158 例检测结果为阳性,在 300 例健康对照者的样本中,有 296 例检测结果为阴性。试剂盒的灵敏度为 92.9%,特异性为 98.7%。疾病发病后第 1 周的阳性率为 77.3%,但从第 9 天开始达到 100%。AUC 和 kappa 系数分别为 0.958 和 0.926,表明该检测结果与标准诊断具有高度一致性。试剂盒的灵敏度不受年龄或性别因素的影响。

结论

本研究开发的 SARS-CoV-2 IgG/IgM 联合抗体检测试剂盒具有快速、简便的特点,性能优越,有助于 COVID-19 的准确诊断和及时治疗与隔离,从而有助于更好地控制全球大流行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c71/7843252/beb4ea4f1f2f/JCLA-35-e23619-g001.jpg

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