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酶免疫测定法与化学发光免疫测定法检测乙型肝炎病毒表面抗原的比较研究

[Comparison study with enzyme immunoassay and chemiluminescence immunoassay for hepatitis B virus surface antigen detection].

作者信息

Huh Hee Jin, Chae Seok-Lae, Cha Young Joo

机构信息

Department of Laboratory Medicine, College of Medicine, Dongguk University, Gyeonggi Province, Korea.

出版信息

Korean J Lab Med. 2007 Oct;27(5):355-9. doi: 10.3343/kjlm.2007.27.5.355.

DOI:10.3343/kjlm.2007.27.5.355
PMID:18094601
Abstract

BACKGROUND

The serological detection of the surface antigen (HBsAg) of hepatitis B virus (HBV) is the basis of detection of HBV infections in blood donors and patients with hepatitis. The aim of this study was to compare the performance of HBsAg enzyme-linked immunosorbent assay (ELISA) and HBsAg chemiluminescence immunoassay used in Korea.

METHODS

We compared seven assays: Architect i2000 (Abbott Laboratories, USA), Elecsys 2010 immunoanalyzer (Roche Diagnostics, Germany), Advia Centaur (Bayer Healthcare, USA), Murex HBsAg version 3 (Abbott Laboratories, USA), Enzygnost HBsAg 5.0 (DADE Behring, Germany), LG HBsAg ELISA (LG, Korea), and Genedia HBsAg ELISA 3.0 (Greencross Medical Science, Korea). We evaluated the sensitivity of each assay by testing serially diluted WHO HBsAg reference material, two seroconversion panels, and recombinant HBsAg with three mutations in the 'a' determinant.

RESULTS

The lowest HBsAg level detected by each assay using WHO reference material was variable from 0.05 (Murex and Advia) to 0.2 IU/mL. When testing 21 seroconversion panels, the total number of positive samples was 15 by Murex and 14 by Architect. Murex, LG, and Architect detected all of the 3 mutant samples tested.

CONCLUSIONS

Analytical sensitivity and mutant detecting ability among HBsAg commercial assays were variable and not related to the analytical methods, but related to the manufacturer's reagents. We suggest that each laboratory should select an HBsAg assay based on analytical performance, test throughput, and the applicability of full automation.

摘要

背景

乙型肝炎病毒(HBV)表面抗原(HBsAg)的血清学检测是献血者和肝炎患者HBV感染检测的基础。本研究旨在比较韩国使用的HBsAg酶联免疫吸附测定(ELISA)和HBsAg化学发光免疫测定的性能。

方法

我们比较了七种检测方法:Architect i2000(美国雅培公司)、Elecsys 2010免疫分析仪(德国罗氏诊断公司)、Advia Centaur(美国拜耳医疗保健公司)、Murex HBsAg版本3(美国雅培公司)、Enzygnost HBsAg 5.0(德国达德拜林公司)、LG HBsAg ELISA(韩国LG公司)和Genedia HBsAg ELISA 3.0(韩国格林十字医学科学公司)。我们通过检测系列稀释的世界卫生组织HBsAg参考物质、两个血清转换样本组以及在“a”决定簇中有三个突变的重组HBsAg来评估每种检测方法的灵敏度。

结果

使用世界卫生组织参考物质时,每种检测方法检测到的最低HBsAg水平各不相同,从0.05(Murex和Advia)到0.2 IU/mL。检测21个血清转换样本组时,Murex检测出的阳性样本总数为15个,Architect为14个。Murex、LG和Architect检测出了所有测试的3个突变样本。

结论

HBsAg商业检测方法之间的分析灵敏度和突变检测能力各不相同,与分析方法无关,而与制造商的试剂有关。我们建议每个实验室应根据分析性能、检测通量和全自动化的适用性来选择HBsAg检测方法。

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