Serological testing for COVID-19

A. Cheepsattayakorn, R. Cheepsattayakorn
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Abstract

The objectives of this study are to identify the rapid, appropriate, screening, definite and novel methods of diagnosis of SARS-CoV-2 (COVID-19) infection, including SARS-CoV-2 (COVID-19) variants among various degree of COVID-19 severity for rapid prevention and control of SARS-CoV-2 (COVID-19) transmission. Methods of The Study: A comprehensive search was carried out in mainstream bibliographic databases or Medical Subject Headings, including ScienDirect, PubMed, Scopus, and ISI Web of Science. The search was applied to the articles that were published between 1971 and early March 2021. Results: With strict literature search and screening processes, it yielded 40 articles from 78 articles of initial literature database. Characteristically, after infection, antibodies are detected in the blood of individuals, particularly individuals with few or mild symptoms. In patients with varying symptoms of COVID-19 and negative results of reverse-transcriptase-polymerase-chain reaction (RT-PCR) tests, the testing has a significantly clinical role when nasopharyngeal swabs are taken more than 5 days after symptom onset. The Royal College of Pathologists (RCPath) developed seven principles for production of a COVID-19 testing strategy. Testing being carried out for a purpose is one of these RCPath’s principles. Nevertheless, denial of requesting SARS-CoV-2 (COVID-19) antibody tests for reassurance should be cautioned. With a lower antibody levels, whether the protective immunity will be sustained is questionable. Several immune-based assays were developed against different SARS-CoV-2 (COVID-19) viral proteins as the followings: 1) Entire Spike (S) protein, IgG antibody from patient serum can cross-react with SARS-CoV and MERS-CoV, 2) S1 subunit of Spike (S) protein, IgA, IgG antibodies from patient serum can cross-react with SARS-CoV only, 3) Receptor-binding domain (RBD), IgG antibody from patient serum can cross-react with SARS-CoV only, and 4) Nucleocapsid (N), IgG antibody from patient serum can cross-react with SARS-CoV only. Long et al demonstrated in their study that IgG antibody and neutralizing antibody levels initiate decreasing within 2-3 months after infection in the majority of persons with recovery from SARS-CoV-2 (COVID-19) infection. An analytical study of the dynamics of neutralizing antibody titers demonstrated reduced neutralizing antibodies around 6-7 weeks after illness onset. In conclusion, the nucleic acid amplification tests may be poorly timed specimen collection, poor-quality specimen collection, long wait times for generating the results, and requirement of trained laboratory technicians. Serological data greatly supplement the laboratory results from the quantitative reverse-transcriptase-polymerase-chain reaction (qRT-PCR), the design of virus elimination programs (seroepidemiology), discovery of the monoclonal antibodies, and development of SARS-CoV-2 (COVID-19) vaccines.
COVID-19血清学检测
本研究旨在探索快速、适宜、筛查、明确、新颖的SARS-CoV-2 (COVID-19)感染诊断方法,包括不同严重程度的SARS-CoV-2 (COVID-19)变异,为快速防控SARS-CoV-2 (COVID-19)传播提供依据。研究方法:在主流书目数据库或医学主题词中进行全面检索,包括ScienDirect、PubMed、Scopus和ISI Web of Science。该搜索适用于1971年至2021年3月初之间发表的文章。结果:经过严格的文献检索和筛选,从初始文献数据库的78篇文章中筛选出40篇。典型的是,在感染后,在个体的血液中检测到抗体,特别是在症状很少或轻微的个体。对于症状各异且RT-PCR检测阴性的新冠肺炎患者,在症状出现后5天以上进行鼻咽拭子检测具有显著的临床意义。英国皇家病理学家学院(RCPath)制定了制定COVID-19检测策略的七项原则。为某个目的而进行的测试是RCPath的原则之一。然而,应谨慎拒绝为保证而要求进行新冠病毒抗体检测。在抗体水平较低的情况下,这种保护性免疫能否持续是值得怀疑的。针对不同的SARS-CoV-2 (COVID-19)病毒蛋白,开发了几种基于免疫的检测方法,如下:1)患者血清Spike (S)蛋白、IgG抗体与SARS-CoV和MERS-CoV均可交叉反应,2)患者血清Spike (S)蛋白S1亚基、IgA、IgG抗体仅与SARS-CoV交叉反应,3)患者血清受体结合域(RBD)、IgG抗体仅与SARS-CoV交叉反应,4)患者血清核衣壳(N)、IgG抗体仅与SARS-CoV交叉反应。Long等人在他们的研究中证明,在大多数SARS-CoV-2 (COVID-19)感染恢复期患者中,IgG抗体和中和抗体水平在感染后2-3个月内开始下降。对中和抗体滴度的动态分析研究表明,在发病后6-7周左右,中和抗体降低。总之,核酸扩增检测存在标本采集时间差、标本采集质量差、结果等待时间长、对实验室技术人员要求高等问题。血清学数据极大地补充了定量逆转录聚合酶链反应(qRT-PCR)、病毒消除程序设计(血清流行病学)、单克隆抗体的发现以及SARS-CoV-2 (COVID-19)疫苗的开发的实验室结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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