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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of commercial enzyme immunoassays for detection of hepatitis delta antigen and anti-hepatitis delta virus (HDV) and immunoglobulin M anti-HDV antibodies.
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Evaluation of commercial enzyme immunoassays for detection of hepatitis delta antigen and anti-hepatitis delta virus (HDV) and immunoglobulin M anti-HDV antibodies.

机译:评价用于检测肝炎三角洲抗原和抗肝炎三角洲病毒(HDV)和免疫球蛋白M抗HDV抗体的商业酶免疫测定法。

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Panels of hepatitis B virus surface antigen-positive sera from drug abusers were used to evaluate 14 commercial enzyme immunoassays from six companies for detecting hepatitis delta virus (HDV) markers. For detecting hepatitis delta virus antigen (HDAg), the Wellcome, Pasteur and Noctech assays had 100% sensitivity for all 42 HDAg-positive serum specimens that were confirmed in-house; the Organon reagents gave 59.5% sensitivity without detergent and 64.3% sensitivity with detergent, but there were 14 discrepant results with and without detergent. The Sorin assay detected HDAg in only 10 of the positive samples (23.8% sensitivity). For the detection of antibody to HDV (anti-HDV) all six commercial enzyme immunoassays were reactive with all 36 anti-HDV-positive specimens that were confirmed in-house. There were no false-positive results with the Wellcome, Noctech, or Sorin assay, but one specimen was false positive by the Organon assay. One HDAg-positive specimen gave a false anti-HDV-positive result in the Abbott assay and an equivocal result in the Pasteur assay (97.8% specificity). For the detection of immunoglobulin M anti-HDV, the Wellcome, Noctech, and Sorin assays agreed for the 38 positives confirmed in-house, except for one false negative with the Sorin test. We conclude that there has been a substantial improvement over previously evaluated assays in sensitivity and specificity of commercial assays for anti-HDV detection, and the sensitivities of immunoglobulin M anti-HDV assays are also comparable. However, there are still major differences in sensitivity among some assays for HDAg detection.
机译:来自吸毒者的乙型肝炎病毒表面抗原阳性血清用于评估六家公司的14种商业酶免疫测定法,以检测肝炎三角洲病毒(HDV)标记。为了检测肝炎三角洲病毒抗原(HDAg),Wellcome,Pasteur和Noctech检测对内部确认的全部42个HDAg阳性血清标本具有100%的敏感性; Organon试剂在不使用去污剂的情况下的灵敏度为59.5%,在使用去污剂的情况下的灵敏度为64.3%,但是使用和不使用去污剂时的灵敏度差异为14。 Sorin分析仅在10个阳性样品中检测到HDAg(灵敏度为23.8%)。为了检测针对HDV的抗体(抗HDV),所有六种商业酶免疫测定均与在内部确认的所有36种抗HDV阳性标本具有反应性。用Wellcome,Noctech或Sorin测定没有假阳性结果,但是通过Organon测定,有一个标本是假阳性。一个HDAg阳性标本在Abbott分析中给出了错误的抗HDV阳性结果,在Pasteur分析中给出了模棱两可的结果(特异性为97.8%)。为了检测免疫球蛋白M抗HDV,Wellcome,Noctech和Sorin分析同意了内部确认的38种阳性结果,但Sorin测试中只有一种假阴性。我们得出的结论是,相对于先前评估的检测方法,在针对抗HDV检测的商业检测方法的敏感性和特异性方面有了实质性的改进,而且免疫球蛋白M抗HDV检测方法的敏感性也相当。但是,在用于HDAg检测的某些检测方法之间,灵敏度的主要差异仍然很大。

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