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乙型肝炎表面抗原检测试剂与首个世界卫生组织乙型肝炎病毒基因型国际参考品的性能评估。

Performance of hepatitis B surface antigen tests with the first WHO international hepatitis B virus genotype reference panel.

机构信息

Section of Molecular Virology, Paul-Ehrlich-Institut, Langen, Germany.

出版信息

J Clin Virol. 2013 Sep;58(1):47-53. doi: 10.1016/j.jcv.2013.06.011. Epub 2013 Jul 3.

Abstract

BACKGROUND

Standardization of hepatitis B surface antigen (HBsAg) tests is indispensable for consistent quality and comparability. Ideally, the assays should detect all known hepatitis B virus (HBV) genotypes equally well.

OBJECTIVE

Development of an HBV genotype reference panel for HBsAg assays representing the most prevalent HBV subgenotypes to address commutability and traceability of the heat-inactivated 2nd WHO International Standard (IS) for HBsAg in relation to native HBsAg and to HBV genotypes.

STUDY DESIGN

An HBV panel of 15 non-inactivated lyophilized specimens representing the subgenotypes A1, A2, B1, B2, C2, D1-D3, E, F2, and H was evaluated in parallel to the IS by 15 laboratories using 19 different HBsAg tests and tree unitages. The virus content of the samples was reduced by ultracentrifugation and dilution to <2×10(4) IU HBV DNA/mL.

RESULTS

Twenty-two qualitative and 6 quantitative data sets were evaluated. Overall, the results demonstrated consistent detection of HBV genotypes by the majority of tests with a mean potency variability relative to the IS of 36%. Some assays showed significant genotype-dependent differences in analytical sensitivity. Some tests were more sensitive with the IS, others less. On average, one IU HBsAg corresponded to 0.88±0.20 ng HBsAg protein.

CONCLUSIONS

The panel was accepted by the WHO as the "1st International Reference Panel for HBV genotypes for HBsAg-based assays". The panel is a helpful complementation to the IS to validate HBV genotype specific analytical test sensitivities.

摘要

背景

乙肝表面抗原(HBsAg)检测的标准化对于保证质量的一致性和结果的可比性至关重要。理想情况下,检测方法应能同等地检测到所有已知的乙型肝炎病毒(HBV)基因型。

目的

开发一个 HBV 基因型参考面板,用于 HBsAg 检测,以涵盖最常见的 HBV 亚型,解决热灭活第 2 届世界卫生组织(WHO)HBsAg 国际标准(IS)与天然 HBsAg 以及 HBV 基因型的可互换性和可溯源性问题。

研究设计

15 个非灭活冻干标本组成的 HBV 面板,代表亚基因型 A1、A2、B1、B2、C2、D1-D3、E、F2 和 H,与 IS 一起由 15 个实验室使用 19 种不同的 HBsAg 检测方法和 3 个单位评估。通过超速离心和稀释,将样品的病毒含量降低至 <2×10(4) IU HBV DNA/mL。

结果

评估了 22 个定性和 6 个定量数据集。总体而言,大多数检测方法都能一致地检测到 HBV 基因型,相对于 IS 的平均效价变异性为 36%。一些检测方法在分析灵敏度上存在显著的基因型依赖性差异。一些检测方法与 IS 相比更敏感,而另一些则不太敏感。平均而言,1 IU HBsAg 相当于 0.88±0.20ng HBsAg 蛋白。

结论

该面板被 WHO 接受为“基于 HBsAg 检测的 HBV 基因型的第 1 个国际参考面板”。该面板是对 IS 的有益补充,可用于验证 HBV 基因型特异性分析检测的灵敏度。

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