Department of Clinical Chemistry, Sestre milosrdnice University Hospital Center, Zagreb, Croatia.
Department of Oncology and Nuclear Medicine, Sestre milosrdnice University Hospital Center, Zagreb, Croatia.
Biochem Med (Zagreb). 2021 Feb 15;31(1):010708. doi: 10.11613/BM.2021.010708.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serological tests have been suggested as an additional diagnostic tool in highly suspected cases with a negative molecular test and determination of seroprevalence in population. We compared the diagnostic performance of eight commercial serological assays for IgA, IgM, and IgG antibodies to the SARS-CoV-2 virus.
The comparison study was performed on a total of 76 serum samples: 30 SARS-CoV-2 polymerase chain reaction (PCR)-negative and 46 SARS-CoV-2 PCR-positive patients with asymptomatic to severe disease and symptoms duration from 3-30 days. The study included: three rapid lateral flow immunochromatographic assays (LFIC), two enzyme-linked immunosorbent assays (ELISA), and three chemiluminescence immunoassays (CLIA).
Agreement between IgM assays were minimal to moderate (kappa 0.26 to 0.63) and for IgG moderate to excellent (kappa 0.72 to 0.92). Sensitivities improved with > 10 days of symptoms and were: 30% to 89% for IgM; 89% to 100% for IgG; 96% for IgA; 100% for IgA/IgM combination; 96% for total antibodies. Overall specificities were: 90% to 100% for IgM; 85% to 100% for IgG; 90% for IgA; 70% for IgA/IgM combination; 100% for total antibodies. Diagnostic accuracy for IgG ELISA and CIA assays were excellent (AUC ≥ 0.90), without significant difference. IgA showed significantly better diagnostic accuracy than IgM (P < 0.001).
There is high variability between IgM assays independently of the assay format, while IgG assays showed moderate to perfect agreement. The appropriate time for testing is crucial for the proper immunity investigation.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)血清学检测已被建议作为分子检测阴性且高度疑似病例的附加诊断工具,并可用于确定人群中的血清流行率。我们比较了 8 种用于检测 SARS-CoV-2 病毒 IgA、IgM 和 IgG 抗体的商业血清学检测的诊断性能。
这项对比研究共纳入 76 份血清样本:30 份 SARS-CoV-2 聚合酶链反应(PCR)阴性样本和 46 份 SARS-CoV-2 PCR 阳性样本,患者的疾病从无症状到重症,症状持续时间为 3-30 天。研究包括:3 种快速侧向流动免疫层析测定法(LFIC)、2 种酶联免疫吸附测定法(ELISA)和 3 种化学发光免疫分析法(CLIA)。
IgM 检测方法之间的一致性为轻度至中度(kappa 值为 0.26-0.63),IgG 检测方法之间的一致性为中度至极好(kappa 值为 0.72-0.92)。症状持续时间超过 10 天时,敏感性有所提高,结果如下:IgM 为 30%-89%;IgG 为 89%-100%;IgA 为 96%;IgA/IgM 联合检测为 100%;总抗体为 96%。总体特异性为:IgM 为 90%-100%;IgG 为 85%-100%;IgA 为 90%;IgA/IgM 联合检测为 70%;总抗体为 100%。IgG ELISA 和 CIA 检测的诊断准确性均非常高(AUC≥0.90),无显著差异。IgA 的诊断准确性明显优于 IgM(P<0.001)。
不同检测方法的 IgM 检测之间存在高度的可变性,而 IgG 检测之间具有中度至极好的一致性。恰当的检测时间对于正确的免疫研究至关重要。