Comparación de dos métodos para la cuantificación en suero de subclases de inmunoglobulinas

Ana Victoria Espinosa , Ana Navas , Juan Molina , Silvia Lagarcha , Rafael Solana , Corona Alonso
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Abstract

Background and aim

The quantification of serum immunoglobulins, and particularly of IgG and IgG subclasses, is of interest for the diagnosis of numerous diseases. The usual detection methods provide different results according to the analyser used. The aim of this study was to compare the results obtained with two different analysers in the measurement of the concentration of IgG and IgG subclasses.

Material and methods

A total of 116 serum samples, regardless of the clinical diagnosis of the patients to whom the samples belonged, were analysed. The analyses were performed on a BNII® System (Siemens Healthcare GmbH, Germany) and Optilite® system (The Binding Site Group Ltd., Birmingham).

Results

The correlation between total IgG concentration (mg/dl) and the sum of the individual IgG subclasses detected was higher using the Optilite® analyser (0.976 vs. 0.866). The percentage of agreement between assays ranged from 43% to 71%, with the lower limit being for the IgG3 agreement. An absence of the usual IgG subclass physiological proportion (IgG1 >IgG2 >IgG3 >IgG4) was detected using BNII®. These findings were a due to the significantly lower proportion of IgG3 obtained by BNII® compared to Optilite® (P< .001), whereas the IgG4 concentration was not significantly different between analysers (P = .117).

Conclusions

Differences between the results obtained with the two different methods suggest that they should not be interchangeable, and that each clinical laboratory should only use one type of analyser. The reference ranges should be standardised according to the results obtained.

两种血清免疫球蛋白亚类定量方法的比较
背景与目的血清免疫球蛋白的定量分析,特别是IgG和IgG亚类的定量分析,对许多疾病的诊断具有重要意义。通常的检测方法根据所使用的分析仪提供不同的结果。本研究的目的是比较两种不同分析仪在IgG和IgG亚类浓度测量中获得的结果。材料与方法对116份血清样本进行分析,不考虑其所属患者的临床诊断。分析采用BNII®系统(Siemens Healthcare GmbH,德国)和Optilite®系统(The Binding Site Group Ltd., Birmingham)。结果Optilite®分析仪检测到的IgG总浓度(mg/dl)与单个IgG亚类之和的相关性较高(0.976比0.866)。测定法之间的一致性百分比从43%到71%不等,下限为IgG3一致性。使用BNII®检测常规IgG亚类生理比例(IgG1 >IgG2 >IgG3 >IgG4)缺失。这些发现是由于BNII®获得的IgG3比例显著低于Optilite®(P<.001),而不同分析仪间IgG4浓度无显著差异(P = .117)。结论两种不同方法所得结果的差异表明它们不应互换,每个临床实验室应只使用一种分析仪。参考范围应根据所得结果进行标准化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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