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Comparison of Six Commercial Diagnostic Tests for the Detection of Dengue Virus Non-Structural-1 Antigen and IgM/IgG Antibodies

机译:登革热病毒非Structural-1抗原和IgM / IgG抗体检测的六种商​​业诊断测试的比较

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摘要

ELISAs and rapid diagnostic tests (RDTs) are widely used for diagnosing dengue virus (DENV) infection. Using 138 single blood samples, we compared the ability to detect non-structural (NS)-1 antigen and anti-DENV IgM/IgG antibodies among (1) DENV Detect NS1 ELISA, DENV Detect IgM capture ELISA and DENV Detect IgG ELISA (InBios International, Inc.); (2) Anti-Dengue virus IgM Human ELISA and Anti-Dengue virus IgG Human ELISA (Abcam); (3) Dengue virus NS1 ELISA, Anti-Dengue virus ELISA (IgM) and Anti-Dengue virus ELISA (IgG) (Euroimmun); (4) Asan Easy Test Dengue NS1 Ag 100 and Asan Easy Test Dengue IgG/IgM (Asan Pharm); (5) SD BIOLINE Dengue Duo (Standard Diagnostics); and (6) Ichroma Dengue NS1 and Ichroma Dengue IgG/IgM (Boditech Med). For NS1 antigen detection, InBios and Euroimmun showed higher sensitivities (100%) than the RDTs (42.9–64.3%). All tests demonstrated variable sensitivities for IgM (38.1–90.5%) and IgG (65.7–100.0%). InBios and Boditech Med demonstrated higher sensitivity (95.6% and 88.2%, respectively) than the other tests for combined NS1 antigen and IgM antibody. Five NS1 antigen tests had good agreement (92.8–98.6%) without showing positivity for chikungunya. However, all IgG tests demonstrated potential false-positivity with variable ranges. Clinical laboratories should note performance variations across tests and potential cross-reactivity.
机译:ELISA和快速诊断测试(RDT)被广泛用于诊断登革热病毒(DENV)感染。我们使用138个单血样本,比较了(1)DENV Detect NS1 ELISA,DENV Detect IgM capture ELISA和DENV Detect IgG ELISA(InBios)中检测非结构性(NS)-1抗原和抗DENV IgM / IgG抗体的能力International,Inc.); (2)抗登革热病毒IgM人ELISA和抗登革热IgG人ELISA(Abcam); (3)登革热病毒NS1 ELISA,抗登革热病毒ELISA(IgM)和抗登革热病毒ELISA(IgG)(Euroimmun); (4)Asan Easy Test Dengue NS1 Ag 100和Asan Easy Test Dengue IgG / IgM(Asan Pharm); (5)SD BIOLINE登革热二重奏(标准诊断); (6)Ichroma Dengue NS1和Ichroma Dengue IgG / IgM(Boditech Med)。对于NS1抗原检测,InBios和Euroimmun显示出比RDT(42.9–64.3%)更高的灵敏度(100%)。所有测试均显示出对IgM(38.1–90.5%)和IgG(65.7–100.0%)的可变敏感性。与联合检测NS1抗原和IgM抗体的其他测试相比,InBios和Boditech Med的敏感性更高(分别为95.6%和88.2%)。五项NS1抗原测试具有良好的一致性(92.8–98.6%),而未显示基孔肯雅病阳性。但是,所有IgG测试均显示了可变范围内的潜在假阳性。临床实验室应注意测试之间的性能差异以及潜在的交叉反应。

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