Department of Clinical Microbiology, Fimlab Laboratories, Tampere, Finland.
Department of Clinical Microbiology, Fimlab Laboratories, Tampere, Finland.
J Virol Methods. 2023 Sep;319:114758. doi: 10.1016/j.jviromet.2023.114758. Epub 2023 May 30.
We evaluated the new 2.0 version of the Roche Diagnostics SARS-CoV-2 Rapid Antigen Test (RAT 2.0) for the detection of SARS-CoV-2. Our evaluation material comprised of nasopharyngeal samples of 140 persons positive for SARS-CoV-2 nucleic acid amplification test (NAAT) and of 100 persons negative for SARS-CoV-2 NAAT. The sensitivity limit of the RAT 2.0 was further estimated with the additional selected samples of 27 persons with high NAAT cycle threshold (Ct) value representing low viral load. For the detection of possible cross-reactions in the RAT 2.0, routine respiratory samples positive for influenza A (N = 5), respiratory syncytial virus (RSV) (N = 4), or combined RSV and human coronavirus OC43 (N = 1) were included in the study material. The overall sensitivity of the RAT 2.0 was 92.1% and specificity 100%. When evaluating the samples with NAAT Ct value ≤ 30, the sensitivity was 97.0%. All samples for cross-reactivity testing containing other viruses instead of SARS-CoV-2 remained negative in RAT 2.0. According to our findings, this RAT 2.0 offers a reliable tool for the diagnostics of acute COVID-19 in this pandemic environment.
我们评估了罗氏诊断 SARS-CoV-2 快速抗原检测(RAT 2.0)新版本,用于检测 SARS-CoV-2。我们的评估材料包括 140 份经 SARS-CoV-2 核酸扩增检测(NAAT)阳性的鼻咽样本和 100 份 SARS-CoV-2 NAAT 阴性的样本。RAT 2.0 的灵敏度限值还通过另外 27 份高 NAAT 循环阈值(Ct)值代表低病毒载量的选定样本进行了进一步估计。为了检测 RAT 2.0 中可能存在的交叉反应,研究材料中包括了 5 份流感 A(N=5)、4 份呼吸道合胞病毒(RSV)或 RSV 和人冠状病毒 OC43 混合阳性(N=1)的常规呼吸道样本。RAT 2.0 的总灵敏度为 92.1%,特异性为 100%。当评估 NAAT Ct 值≤30 的样本时,灵敏度为 97.0%。所有用于交叉反应测试的包含其他病毒而不是 SARS-CoV-2 的样本在 RAT 2.0 中仍为阴性。根据我们的发现,这种 RAT 2.0 在当前大流行环境下为急性 COVID-19 的诊断提供了可靠的工具。