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Sensitivities of Four New Commercial Hepatitis B Virus Surface Antigen (HBsAg) Assays in Detection of HBsAg Mutant Forms

机译:四种新的商业乙型肝炎病毒表面抗原(HBsAg)检测方法在检测HBsAg突变体形式中的敏感性

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Mutations in hepatitis B virus surface antigen (HBsAg) involving amino acid substitution within the immunodominant “a” determinant may affect the performance of commercial HBsAg assays. The performances of four HBsAg assays that recently received Conformité Européene marking, Advia Centaur HBsAg (Bayer), Monolisa HBsAg Ultra (Bio-Rad), Liaison HBsAg (Dia Sorin), and Vidas HBsAg Ultra (bioMérieux), were compared with that of the routinely used HBsAg assay AxSYM HBsAg V2 (Abbott). Assays were evaluated for (i) analytical sensitivity performance with a national reference HBsAg panel (including 10 samples with calibrated HBsAg concentrations from 0.04 to 2.24 ng/ml) and (ii) the detection of HBsAg mutants by studying a panel of 35 HBsAg mutants (23 collected from patients and 12 recombinant mutants). The limits of detection of these assays were <0.15 ng/ml (from 0.089 to 0.121 ng/ml). The sensitivity performances for mutant virus detection varied, ranging from 37.1% to 91.4%. The lack of detection of these mutants by commercial assays was probably due to the epitope recognition of the anti-HBs assay reagents in the capture phase and in the conjugates. The prevalence and clinical impact of HBsAg mutants are under investigation. However, the manufacturers must be vigilant in the design of the assays in order to reduce the risk of missing a broad range of described S gene mutants.
机译:乙型肝炎病毒表面抗原(HBsAg)的突变涉及免疫显性“ a”决定簇内的氨基酸取代,可能会影响商业性HBsAg分析的性能。将最近获得欧洲标准认证的四个HBsAg检测,Advia Centaur HBsAg(拜耳),Monolisa HBsAg Ultra(Bio-Rad),Liaison HBsAg(Dia Sorin)和Vidas HBsAg Ultra(bioMérieux)的性能进行了比较。常规使用HBsAg分析AxSYM HBsAg V2(Abbott)。 (i)使用国家参考HBsAg专家组(包括10个HBsAg校准浓度为0.04至2.24 ng / ml的样品)和(ii)通过研究35个HBsAg突变体的组(从患者中收集了23个和12个重组突变体。这些测定的检出限为<0.15 ng / ml(0.089至0.121 ng / ml)。突变病毒检测的敏感度范围从37.1%到91.4%不等。通过商业化检测缺乏对这些突变体的检测可能是由于在捕获阶段和结合物中抗-HBs检测试剂的表位识别。 HBsAg突变体的患病率及其临床影响正在研究中。但是,制造商必须在试验设计中保持警惕,以减少错过广泛描述的S基因突变体的风险。

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