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Performance Evaluation of Different Commercial Serological Kits for Diagnosis of Acute Hepatitis E Viral Infection

机译:不同商业血清学试剂盒诊断急性戊型肝炎病毒感染的性能评估

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摘要

Clinical diagnosis of hepatitis E viral (HEV) infection mainly relies on serological assays, and the current status of misdiagnoses regarding HEV infection is uncertain. In this study, patients with acute HEV infection were tested for anti-HEV IgM and IgG, a HEV antigen (Ag), and viral loads (HEV RNA). Serology was performed using four commercial HEV ELISA kits: Wantai, Kehua, Lizhu, and Genelabs IgM and IgG. The HEV RNA was detected using RT-PCR assays. The sensitivities of different kits for anti-HEV IgM ranged from 82.6% to 86%. Each kit for anti-HEV IgM was highly specific (97.8–100%). The sensitivities of all kits to detect anti-HEV IgG with (87.2–91.9%) had a substantial agreement, but the Kehua and Genelabs tests were more specific than the Wantai and Lizhu tests. The Wantai tests for the HEV Ag and HEV RNA were also important for acute HEV infections (Kappa = 0.787). Furthermore, a total of 6.98% of HEV infections were positive for HEV RNA but negative for both the HEV Ag and anti-HEV antibodies of IgM and IgG classes. Our findings demonstrate that the diagnosis of hepatitis E may be missed if only serological assays are used. Thus, a combination of serological and nucleic acid testing provides the optimal sensitivity and specificity to the diagnostic process.
机译:戊型肝炎病毒(HEV)感染的临床诊断主要依靠血清学检测,关于HEV感染的误诊现状尚不确定。在这项研究中,对急性HEV感染的患者进行了抗HEV IgM和IgG,HEV抗原(Ag)和病毒载量(HEV RNA)的测试。使用四种市售的HEV ELISA试剂盒进行血清学检测:Wantai,Kehua,Lizhu和Genelabs IgM和IgG。使用RT-PCR测定法检测HEV RNA。不同试剂盒对抗HEV IgM的敏感性范围为82.6%至86%。每个抗HEV IgM试剂盒都是高度特异性的(97.8–100%)。所有试剂盒检测抗-HEV IgG(87.2–91.9%)的敏感性基本一致,但是Kehua和Genelabs测试比万代和Lizhu测试更具特异性。对戊型肝炎病毒和戊型肝炎病毒RNA的万代检测对于急性戊型肝炎病毒感染也很重要(Kappa = 0.787)。此外,总共6.98%的HEV感染对HEV RNA呈阳性,但对IgM和IgG类的HEV Ag和抗HEV抗体均为阴性。我们的发现表明,如果仅使用血清学检测,可能会漏诊戊型肝炎。因此,血清学和核酸测试的结合为诊断过程提供了最佳的敏感性和特异性。

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