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用于新冠病毒疾病诊断的逆转录聚合酶链反应检测的最新进展与挑战

Recent advances and challenges of RT-PCR tests for the diagnosis of COVID-19.

作者信息

Teymouri Manoucher, Mollazadeh Samaneh, Mortazavi Hamed, Naderi Ghale-Noie Zari, Keyvani Vahideh, Aghababaei Farzaneh, Hamblin Michael R, Abbaszadeh-Goudarzi Ghasem, Pourghadamyari Hossein, Hashemian Seyed Mohammad Reza, Mirzaei Hamed

机构信息

Natural Products and Medicinal Plants Research Center, North Khorasan University of Medical Sciences, Bojnurd, Iran.

Natural Products and Medicinal Plants Research Center, North Khorasan University of Medical Sciences, Bojnurd, Iran.

出版信息

Pathol Res Pract. 2021 May;221:153443. doi: 10.1016/j.prp.2021.153443. Epub 2021 Apr 14.

Abstract

Since the outbreak of the novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the control of virus spread has remained challenging given the pitfalls of the current diagnostic tests. Nevertheless, RNA amplification techniques have been the gold standard among other diagnostic methods for monitoring clinical samples for the presence of the virus. In the current paper, we review the shortcomings and strengths of RT-PCR (real-time polymerase chain reaction) techniques for diagnosis of coronavirus disease (COVID)-19. We address the repercussions of false-negative and false-positive rates encountered in the test, summarize approaches to improve the overall sensitivity of this method. We discuss the barriers to the widespread use of the RT-PCR test, and some technical advances, such as RT-LAMP (reverse-transcriptase-loop mediated isothermal amplification). We also address how other molecular techniques, such as immunodiagnostic tests can be used to avoid incorrect interpretation of RT-PCR tests.

摘要

自新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)爆发以来,鉴于当前诊断测试存在的缺陷,控制病毒传播一直具有挑战性。然而,在监测临床样本中病毒存在的其他诊断方法中,RNA扩增技术一直是金标准。在本文中,我们回顾了用于诊断冠状病毒病(COVID)-19的逆转录聚合酶链反应(RT-PCR)技术的缺点和优点。我们探讨了该测试中出现的假阴性和假阳性率的影响,总结了提高该方法总体灵敏度的方法。我们讨论了RT-PCR测试广泛应用的障碍以及一些技术进展,如逆转录环介导等温扩增(RT-LAMP)。我们还探讨了如何使用其他分子技术,如免疫诊断测试,来避免对RT-PCR测试的错误解读。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da92/8045416/e54434a75265/gr1_lrg.jpg

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