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相似但不一致:重新审视不同检测方法检测IgG亚类的陷阱

Similar but not consistent: Revisiting the pitfalls of measuring IgG subclasses with different assays.

作者信息

Ludwig-Kraus Beatrice, Kraus Frank Bernhard

机构信息

Zentrallabor, Department of Laboratory Medicine, University Hospital Halle, Halle (Saale), Germany.

Department of Biology, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.

出版信息

J Clin Lab Anal. 2017 Nov;31(6). doi: 10.1002/jcla.22146. Epub 2017 Jan 16.

Abstract

BACKGROUND

Laboratory quantification of IgG subclasses (IgGSc) is a well-established second-line tool for differential diagnosis of immune deficiencies. However, so far there is still no internationally approved standard available for IgGSc, and different assays are prone to produce divergent results. In this study, we evaluated the comparability and equivalence of two commercially available IgGSc assays, one being the Siemens IgGSc assay on a BN ProSpec analyzer and the other being The Binding Site (TBS) IgGSc assay on a Roche cobas c502 analyzer.

METHODS

We analyzed a total of 50 patient plasma samples obtained over a 3-month period with both IgGSc assays and compared the resulting data based and the CLSI EP09-A3 method comparison guideline.

RESULTS

Depending on the analyzed IgGSc type, the average relative differences in IgGSc concentration (g/L) between the two assays were considerable, starting with -13.5% for IgG1 and 11.3% for IgG2, over -47.3% for IgG4, and up to 52.9% for IgG3. Applying the assay-specific reference intervals, the classification agreement (below, within, or above the reference range) ranged from 88% to 90% for the individual subclasses. However, only 68% of samples showed an overall classification agreement.

CONCLUSION

The comparability of the two IgGSc assays proved to be limited and might be considered similar at best on the diagnostic level. Laboratory specialists as well as clinicians therefore should be cautious when using and interpreting IgGSc measurements obtained with different assays or analyzers.

摘要

背景

IgG亚类(IgGSc)的实验室定量检测是免疫缺陷鉴别诊断中一项成熟的二线工具。然而,到目前为止,仍没有国际认可的IgGSc标准,不同检测方法容易产生不同结果。在本研究中,我们评估了两种市售IgGSc检测方法的可比性和等效性,一种是西门子在BN ProSpec分析仪上的IgGSc检测方法,另一种是The Binding Site(TBS)在罗氏cobas c502分析仪上的IgGSc检测方法。

方法

我们使用两种IgGSc检测方法分析了在3个月期间获得的总共50份患者血浆样本,并根据CLSI EP09 - A3方法比较指南比较了所得数据。

结果

根据所分析的IgGSc类型,两种检测方法之间IgGSc浓度(g/L)的平均相对差异相当大,IgG1起始为-13.5%,IgG2为11.3%,IgG4为-47.3%,IgG3高达52.9%。应用特定检测方法的参考区间,各个亚类的分类一致性(低于、在或高于参考范围)在88%至90%之间。然而,只有68%的样本显示总体分类一致。

结论

两种IgGSc检测方法的可比性有限,在诊断水平上充其量只能认为是相似的。因此,实验室专家和临床医生在使用和解释通过不同检测方法或分析仪获得的IgGSc测量结果时应谨慎。

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