Department of Medical Microbiology, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Influenza Other Respir Viruses. 2022 Nov;16(6):1033-1039. doi: 10.1111/irv.13048. Epub 2022 Sep 6.
The rapid diagnostics tests for SARS-CoV-2 antigen vary in their sensitivities, and moreover, genomic mutations may further affect the performance of the assays. We aimed to evaluate the analytical performance of an automated antigen assay and compare its sensitivity in Delta- and Omicron-variant positive clinical samples.
The analytical performance of an automated mariPOC SARS-CoV-2 antigen test was evaluated on a population of community-dwelling subjects with mild respiratory symptoms or being asymptomatic investigated by the RT-qPCR Allplex™ SARS-CoV-2 assay. The sensitivity and specificity of the antigen test were evaluated on prospective 621 nasopharyngeal swabs along with oropharyngeal swabs. The sensitivity regarding variants determined by the Allplex™ SARS-CoV-2 Variant assays was analysed in additional, retrospective 158 Delta and 59 Omicron samples.
The overall sensitivity of the antigen test in prospective samples was 77.9% (113/145; 95% confidence interval [CI] 70.3-84.4) with the specificity of 99.8% (95% CI 98.8-100). Regarding the variant, the sensitivity was higher in Omicron-variant samples, 93.2% (55/59; 95% CI 83.5-98.1), compared to Delta-variant samples, 71.5% (113/158; 95% CI 63.8-78.4; p = .001).
In community-dwelling subjects with mild respiratory symptoms or being asymptomatic, the automated mariPOC SARS-CoV-2 antigen test showed high sensitivity over 98.0% in subgroup samples with cycle threshold (Ct) values < 25. Regarding the variant, the antigen test sensitivity was higher in the Omicron-variant samples compared to the Delta-variant samples. The analytical performance of the antigen test can differ between the SARS-CoV-2 variants, and a re-evaluation should be performed for new circulating lineages.
SARS-CoV-2 抗原的快速诊断检测在敏感性上存在差异,此外,基因组突变可能进一步影响检测的性能。我们旨在评估一种自动化抗原检测的分析性能,并比较其在 Delta 和 Omicron 变异阳性临床样本中的敏感性。
我们评估了一种自动化 mariPOC SARS-CoV-2 抗原检测在社区居住的有轻度呼吸道症状或无症状的人群中的分析性能,这些人群通过 RT-qPCR Allplex SARS-CoV-2 检测进行了调查。前瞻性的 621 例鼻咽拭子和咽拭子检测了抗原检测的敏感性和特异性。此外,还分析了 158 例 Delta 和 59 例 Omicron 样本中 Allplex SARS-CoV-2 变异检测确定的变异体的敏感性。
前瞻性样本中抗原检测的总体敏感性为 77.9%(113/145;95%置信区间 [CI] 70.3-84.4),特异性为 99.8%(95% CI 98.8-100)。关于变异体,与 Delta 变异体样本相比,Omicron 变异体样本中的敏感性更高,为 93.2%(55/59;95% CI 83.5-98.1),而 Delta 变异体样本为 71.5%(113/158;95% CI 63.8-78.4;p=0.001)。
在有轻度呼吸道症状或无症状的社区居住的人群中,自动化 mariPOC SARS-CoV-2 抗原检测在 Ct 值<25 的亚组样本中表现出超过 98.0%的高敏感性。关于变异体,与 Delta 变异体样本相比,Omicron 变异体样本中的抗原检测敏感性更高。抗原检测的分析性能可能在 SARS-CoV-2 变异体之间存在差异,因此对于新的流行谱系应重新评估。