Lefever Stefanie, Indevuyst Christophe, Cuypers Lize, Dewaele Klaas, Yin Nicolas, Cotton Frédéric, Padalko Elizaveta, Oyaert Matthijs, Descy Julie, Cavalier Etienne, Van Ranst Marc, André Emmanuel, Lagrou Katrien, Vermeersch Pieter
Clinical Department of Laboratory Medicine and National Reference Center for Respiratory Pathogens, University Hospitals Leuven, Leuven, Belgium.
Clinical Laboratory, Medisch Centrum Huisartsen, Leuven, Belgium.
J Clin Microbiol. 2021 Jun 18;59(7):e0037421. doi: 10.1128/JCM.00374-21.
We evaluated the quantitative DiaSorin Liaison severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen test in symptomatic and asymptomatic individuals consulting their general practitioners (GPs) during a period of stable intense virus circulation (213/100,000 habitants per day). Leftover reverse transcription-PCR (RT-PCR) positive ( = 204) and negative ( = 210) nasopharyngeal samples were randomly selected among fresh routine samples collected from patients consulting their GPs. Samples were tested on Liaison XL according to the manufacturer's instructions. Equivocal results were considered negative. The overall sensitivity and specificity of the Liaison antigen test compared to RT-PCR were 65.7% (95% confidence interval [CI], 58.9% to 71.9%) and 100% (CI, 97.8% to 100%). Sensitivity in samples with viral loads of ≥10, ≥10, and ≥10 copies/ml were 100% (CI, 96.3% to 100.0%), 96.5% (CI, 91.8% to 98.7%), and 87.4% (CI, 81.3% to 91.5%), respectively. All samples with ≤10 copies/ml were antigen negative. The ratio of antigen concentration to viral load in samples with ≥10 copies/ml was comparable in symptomatic and asymptomatic individuals (0.58). The proportion of RT-PCR-positive participants with a high viral load (≥10 copies/ml) was not significantly higher in symptomatic than in asymptomatic participants (63.9% [CI, 54.9% to 72.0%] versus 51.9% [CI, 41.1% to 62.6%]; 0.11), but the proportion of participants with a low viral load (<10 copies/ml) was significantly higher in asymptomatic than in symptomatic RT-PCR-positive participants (35.4% [CI, 25.8% to 46.4%] versus 14.3% [CI, 9.0% to 21.8%]; 0.01). Sensitivity and specificity in samples with a viral load of ≥10 copies/ml were 96.5% and 100%. The correlation of antigen concentration with viral load was comparable in symptomatic and asymptomatic individuals.
我们评估了DiaSorin Liaison严重急性呼吸综合征冠状病毒2(SARS-CoV-2)抗原定量检测,检测对象为在病毒稳定高强度传播期间(每天每10万居民中有213例)咨询全科医生(GP)的有症状和无症状个体。从咨询全科医生的患者的新鲜常规样本中随机选取剩余的逆转录聚合酶链反应(RT-PCR)阳性(n = 204)和阴性(n = 210)鼻咽样本。根据制造商说明在Liaison XL上对样本进行检测。结果不明确的视为阴性。与RT-PCR相比,Liaison抗原检测的总体敏感性和特异性分别为65.7%(95%置信区间[CI],58.9%至71.9%)和100%(CI,97.8%至100%)。病毒载量≥10³、≥10⁴和≥10⁵拷贝/毫升的样本中的敏感性分别为100%(CI,96.3%至100.0%)、96.5%(CI,91.8%至98.7%)和87.4%(CI,81.3%至91.5%)。所有病毒载量≤10³拷贝/毫升的样本抗原均为阴性。有症状和无症状个体中病毒载量≥10³拷贝/毫升的样本中抗原浓度与病毒载量的比值相当(0.58)。有症状的RT-PCR阳性参与者中病毒载量高(≥10⁵拷贝/毫升)的比例并不显著高于无症状参与者(63.9%[CI,54.9%至72.0%]对51.9%[CI,41.1%至62.6%];P = 0.11),但无症状的RT-PCR阳性参与者中病毒载量低(<10³拷贝/毫升)的比例显著高于有症状参与者(35.4%[CI,25.8%至46.4%]对14.3%[CI,9.0%至21.8%];P = 0.01)。病毒载量≥10³拷贝/毫升的样本中的敏感性和特异性分别为96.5%和100%。有症状和无症状个体中抗原浓度与病毒载量的相关性相当。