Favresse Julien, Gillot Constant, Oliveira Maxime, Cadrobbi Julie, Elsen Marc, Eucher Christine, Laffineur Kim, Rosseels Catherine, Van Eeckhoudt Sandrine, Nicolas Jean-Baptiste, Morimont Laure, Dogné Jean-Michel, Douxfils Jonathan
Department of Laboratory Medicine, Clinique St-Luc Bouge, 5004 Namur, Belgium.
Department of Pharmacy, Namur Research Institute for Life Sciences, University of Namur, 5000 Namur, Belgium.
J Clin Med. 2021 Jan 13;10(2):265. doi: 10.3390/jcm10020265.
(1) Background: The detection of SARS-CoV-2 RNA in nasopharyngeal samples through real-time reverse transcription-polymerase chain reaction (RT-PCR) is considered the standard gold method for the diagnosis of SARS-CoV-2 infection. Antigen detection (AD) tests are more rapid, less laborious, and less expensive alternatives but still require clinical validation. (2) Methods: This study compared the clinical performance of five AD tests, including four rapid AD (RAD) tests (biotical, Panbio, Healgen, and Roche) and one automated AD test (VITROS). For that purpose, 118 (62.8%) symptomatic patients and 70 (37.2%) asymptomatic subjects were tested, and results were compared to RT-PCR. (3) Results: The performance of the RAD tests was modest and allowed us to identify RT-PCR positive patients with higher viral loads. For Ct values ≤25, the sensitivity ranged from 93.1% (95% CI: 83.3-98.1%) to 96.6% (95% CI: 88.1-99.6%), meaning that some samples with high viral loads were missed. Considering the Ct value proposed by the CDC for contagiousness (i.e., Ct values ≤33) sensitivities ranged from 76.2% (95% CI: 65.4-85.1%) to 88.8% (95% CI: 79.7-94.7%) while the specificity ranged from 96.3% (95% CI: 90.8-99.0%) to 99.1% (95% CI: 95.0-100%). The VITROS automated assay showed a 100% (95% CI: 95.5-100%) sensitivity for Ct values ≤33, and had a specificity of 100% (95% CI: 96.6-100%); (4) Conclusions: Compared to RAD tests, the VITROS assay fully aligned with RT-PCR for Ct values up to 33, which might allow a faster, easier and cheaper identification of SARS-CoV-2 contagious patients.
(1)背景:通过实时逆转录聚合酶链反应(RT-PCR)检测鼻咽样本中的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)RNA被认为是诊断SARS-CoV-2感染的标准金标准方法。抗原检测(AD)试验是更快速、省力且成本更低的替代方法,但仍需要临床验证。(2)方法:本研究比较了五种AD试验的临床性能,包括四种快速AD(RAD)试验(碧迪、Panbio、海基伦和罗氏)和一种自动化AD试验(VITROS)。为此,对118名(62.8%)有症状患者和70名(37.2%)无症状受试者进行了检测,并将结果与RT-PCR进行比较。(3)结果:RAD试验的性能一般,能让我们识别出病毒载量较高的RT-PCR阳性患者。对于Ct值≤25,敏感性范围为93.1%(95%置信区间:83.3-98.1%)至96.6%(95%置信区间:88.1-99.6%),这意味着一些高病毒载量的样本被漏检。考虑到美国疾病控制与预防中心(CDC)提出的具有传染性的Ct值(即Ct值≤33),敏感性范围为76.2%(95%置信区间:65.4-85.1%)至88.8%(95%置信区间:79.7-94.7%),而特异性范围为96.3%(95%置信区间:90.8-99.0%)至99.1%(95%置信区间:95.0-100%)。VITROS自动化检测对Ct值≤33的敏感性为100%(95%置信区间:95.5-100%),特异性为100%(95%置信区间:96.6-100%);(4)结论:与RAD试验相比,VITROS检测对于Ct值高达33的情况与RT-PCR完全一致,这可能有助于更快、更简便且更经济地识别SARS-CoV-2传染性患者。