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J Clin Lab Anal. 2022 Jul;36(7):e24485. doi: 10.1002/jcla.24485. Epub 2022 May 25.
2
Safety, tolerability and viral kinetics during SARS-CoV-2 human challenge in young adults.在年轻成年人中进行 SARS-CoV-2 人体挑战的安全性、耐受性和病毒动力学。
Nat Med. 2022 May;28(5):1031-1041. doi: 10.1038/s41591-022-01780-9. Epub 2022 Mar 31.
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Rapid Diagnostic Testing for SARS-CoV-2.新型冠状病毒2019(SARS-CoV-2)的快速诊断检测
N Engl J Med. 2022 Jan 20;386(3):264-272. doi: 10.1056/NEJMcp2117115. Epub 2022 Jan 7.
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OMICRON (B.1.1.529): A new SARS-CoV-2 variant of concern mounting worldwide fear.奥密克戎(B.1.1.529):一种引起全球恐慌的新型关注变异株。
J Med Virol. 2022 May;94(5):1821-1824. doi: 10.1002/jmv.27541. Epub 2021 Dec 30.
5
Clinical Assessment of the DiaSorin LIAISON SARS-CoV-2 Ag Chemiluminescence Immunoassay.索林LIAISON SARS-CoV-2抗原化学发光免疫分析的临床评估
EJIFCC. 2021 Jun 29;32(2):216-223. eCollection 2021 Jun.
6
[Evaluation of a Visually-Read Rapid Antigen Test Kit (SGA V-Chek) for Detection of SARS-CoV-2 Virus].[用于检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒的视觉读取快速抗原检测试剂盒(SGA V-Chek)的评估]
Mikrobiyol Bul. 2021 Jul;55(3):461-464. doi: 10.5578/mb.20219815.
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Comparison of four commercial, automated antigen tests to detect SARS-CoV-2 variants of concern.比较四种商业化的自动化抗原检测试剂对检测 SARS-CoV-2 关注变异株的效果。
Med Microbiol Immunol. 2021 Dec;210(5-6):263-275. doi: 10.1007/s00430-021-00719-0. Epub 2021 Aug 20.
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Evaluation of accuracy, exclusivity, limit-of-detection and ease-of-use of LumiraDx™: An antigen-detecting point-of-care device for SARS-CoV-2.评估 LumiraDx™ 的准确性、排他性、检测限和易用性:一种用于 SARS-CoV-2 的抗原检测即时检测设备。
Infection. 2022 Apr;50(2):395-406. doi: 10.1007/s15010-021-01681-y. Epub 2021 Aug 12.
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A Real-World Comparison of SARS-CoV-2 Rapid Antigen Testing versus PCR Testing in Florida.佛罗里达州严重急性呼吸综合征冠状病毒2型快速抗原检测与聚合酶链反应检测的真实世界比较
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10
High Performance of SARS-Cov-2N Protein Antigen Chemiluminescence Immunoassay as Frontline Testing for Acute Phase COVID-19 Diagnosis: A Retrospective Cohort Study.严重急性呼吸综合征冠状病毒2 N蛋白抗原化学发光免疫测定在新型冠状病毒肺炎急性期诊断一线检测中的高性能:一项回顾性队列研究
Front Med (Lausanne). 2021 Jul 14;8:676560. doi: 10.3389/fmed.2021.676560. eCollection 2021.

新型冠状病毒核衣壳蛋白在实验室诊断中的应用。

The utility of SARS-CoV-2 nucleocapsid protein in laboratory diagnosis.

机构信息

Class 11, Grade 2018, Medical School of Zhengzhou University, Zhengzhou, China.

Department of Laboratory Medicine, Zhongnan Hospital, Wuhan University, Wuhan, China.

出版信息

J Clin Lab Anal. 2022 Jul;36(7):e24534. doi: 10.1002/jcla.24534. Epub 2022 Jun 3.

DOI:10.1002/jcla.24534
PMID:35657146
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9279953/
Abstract

BACKGROUND

The Coronavirus Disease 2019 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which has now become a global pandemic owing to its high transmissibility. The SARS-CoV-2 nucleocapsid protein tests are playing an important role in screening and diagnosing patients with COVID-19, and studies about the utility of SARS-CoV-2 nucleocapsid protein tests are increasing now.

METHODS

In this review, all the relevant original studies were assessed by searching in electronic databases including Scopus, Pubmed, Embase, and Web of Science. "SARS-CoV-2", "COVID-19", "nucleocapsid protein", and "antigen detection" were used as keywords.

RESULTS

In this review, we summarized the utility of SARS-CoV-2 nucleocapsid protein in laboratory diagnosis. Among the representative researches, this review analyzed, the sensitivity of SARS-CoV-2 nucleocapsid protein detection varies from 13% to 87.9%, while the specificity could almost reach 100% in most studies. As a matter of fact, the sensitivity is around 50% and could be higher or lower due to the influential factors.

CONCLUSION

It is well suggested that SARS-CoV-2 nucleocapsid protein is a convenient method with a short turnaround time of about half an hour, and the presence of N antigen is positively related to viral transmissibility, indicating that SARS-CoV-2 N protein immunoassays contribute to finding out those infected people rapidly and segregating them from the uninfected people.

摘要

背景

新型冠状病毒病(COVID-19)由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起,由于其高传染性,现已成为全球性大流行。SARS-CoV-2 核衣壳蛋白检测在筛选和诊断 COVID-19 患者方面发挥着重要作用,目前关于 SARS-CoV-2 核衣壳蛋白检测效用的研究正在增加。

方法

本综述通过在 Scopus、Pubmed、Embase 和 Web of Science 等电子数据库中搜索,评估了所有相关的原始研究。使用了“SARS-CoV-2”、“COVID-19”、“核衣壳蛋白”和“抗原检测”作为关键词。

结果

在本综述中,我们总结了 SARS-CoV-2 核衣壳蛋白在实验室诊断中的效用。在我们分析的代表性研究中,SARS-CoV-2 核衣壳蛋白检测的敏感性从 13%到 87.9%不等,而特异性在大多数研究中几乎可达 100%。事实上,由于影响因素的存在,敏感性约为 50%,可能更高或更低。

结论

建议将 SARS-CoV-2 核衣壳蛋白作为一种方便的方法,其检测周转时间约为半小时,N 抗原的存在与病毒传播性呈正相关,这表明 SARS-CoV-2 N 蛋白免疫测定有助于快速发现感染者并将其与未感染者隔离。