Krempe Friederike, Schöler Lara, Katschinski Benjamin, Herrmann Anke, Anastasiou Olympia E, Elsner Carina, Ross R Stefan, Scholz Friedrich, Dittmer Ulf, Miethe Peter, Le-Trilling Vu Thuy Khanh, Trilling Mirko
Institute for Virology, University Hospital Essen, University of Duisburg-Essen, 45147 Essen, North Rhine-Westphalia, Germany.
Senova Gesellschaft für Biowissenschaft und Technik mbH, 99427 Weimar, Germany.
iScience. 2021 Oct 22;24(10):103194. doi: 10.1016/j.isci.2021.103194. Epub 2021 Sep 30.
The COVID-19 pandemic poses enormous challenges to global healthcare sectors. To prevent the overburden of medical systems, it is crucial to distinguish individuals approaching the most infectious early phase from those in the declining non-infectious phase. However, a large fraction of transmission events occur during pre- or asymptomatic phases. Especially in the absence of symptoms, it is difficult to distinguish prodromal from late phases of infection just by RT-PCR since both phases are characterized by low viral loads and corresponding high Ct values (>30). We evaluated a new rapid test detecting IgG antibodies recognizing SARS-CoV-2 nucleocapsid protein using two commercial antibody assays and an in-house neutralization test before determining suitability for testing clinical swab material. Our analyses revealed the combination of the well-known RT-PCR and the new rapid antibody test using one single clinical nasopharyngeal swab specimen as a fast, cost-effective, and reliable way to discriminate prodromal from subsiding phases of COVID-19.
新冠疫情给全球医疗行业带来了巨大挑战。为防止医疗系统不堪重负,区分处于传染性最强早期阶段的个体与处于传染性下降的非感染阶段的个体至关重要。然而,很大一部分传播事件发生在症状出现前或无症状阶段。特别是在没有症状的情况下,仅通过逆转录聚合酶链反应(RT-PCR)很难区分感染前驱期和后期,因为这两个阶段的病毒载量都很低,相应的循环阈值(Ct)值较高(>30)。在确定其对临床拭子材料检测的适用性之前,我们使用两种商业抗体检测方法和一项内部中和试验,评估了一种检测识别新冠病毒核衣壳蛋白的IgG抗体的新型快速检测方法。我们的分析表明,将广为人知的RT-PCR与新型快速抗体检测相结合,使用单个临床鼻咽拭子标本,是区分新冠感染前驱期和消退期的一种快速、经济高效且可靠的方法。