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人IgG亚类的散射比浊法测量及其参考范围。

Nephelometric measurements of human IgG subclasses and their reference ranges.

作者信息

Vlug A, Nieuwenhuys E J, van Eijk R V, Geertzen H G, van Houte A J

机构信息

Central Laboratory of the Netherlands, Red Cross Blood Transfusion Service, University of Amsterdam.

出版信息

Ann Biol Clin (Paris). 1994;52(7-8):561-7.

PMID:7840433
Abstract

IgG subclass measurements are generally performed with the radial immunodiffusion (RID) technique. With this method, results are obtained after an incubation period of 48-72 hours. We developed nephelometric assays on the Behring Nephelometer Analyzer (BNA) that allow a quantification of IgG subclass concentrations in a large number of samples quickly (less than 15 minutes for a complete IgG subclass profile) and reproducibly (intra-assay variation 2.5-5.5%, interassay variation 3.4-6.0% and inter-lab variation 5.4-10.3%). The nephelometric method was compared with the RID technique by analyzing the IgG subclass levels in sixty selected samples. For all IgG subclasses identical results and high correlation coefficients (r > 0.93) were found. In addition, the detection limits of the nephelometric method for all four IgG subclasses were identical or lower than those of the RID technique. Furthermore, the interlab variations of the nephelometric IgG subclass assays are lower than those of the RID method. However, the major advantages of the nephelometric assay are the speed, the minimal workload (automated IgG subclass determinations) and the possibility for automated bidirectional data transmission. Recently we have established new reference ranges for the human IgG subclasses in sera of adults and children. In order to validate these reference values we have measured the IgG subclasses in sera from 112 healthy children with the nephelometric method. In 1992, more than 2000 patient sera were tested by the nephelometric assay. A predominance of IgG2 abnormality was observed. In 9.8% of these sera the IgG2 concentration was decreased. Elevated IgG2 concentrations were found in 1.9% of the sera. Furthermore, the sum of the quantitated four IgG subclasses was similar to that of total IgG (less than 20% difference).

摘要

IgG亚类检测通常采用放射免疫扩散(RID)技术进行。使用这种方法,在48 - 72小时的孵育期后可获得结果。我们在贝林散射比浊分析仪(BNA)上开发了比浊测定法,该方法能够快速(完整的IgG亚类分析少于15分钟)且可重复地(批内变异2.5 - 5.5%,批间变异3.4 - 6.0%,实验室间变异5.4 - 10.3%)定量大量样本中的IgG亚类浓度。通过分析60个选定样本中的IgG亚类水平,将比浊法与RID技术进行了比较。对于所有IgG亚类,均发现结果相同且相关系数较高(r > 0.93)。此外,比浊法对所有四种IgG亚类的检测限与RID技术相同或更低。而且,比浊法IgG亚类检测的实验室间变异低于RID法。然而,比浊测定法的主要优点是速度快、工作量最小(自动进行IgG亚类测定)以及能够进行自动双向数据传输。最近我们已经建立了成人和儿童血清中人类IgG亚类的新参考范围。为了验证这些参考值,我们用比浊法测量了112名健康儿童血清中的IgG亚类。1992年,通过比浊测定法检测了2000多份患者血清。观察到IgG2异常占优势。在这些血清中,9.8%的血清IgG2浓度降低。1.9%的血清中发现IgG2浓度升高。此外,定量的四种IgG亚类的总和与总IgG相似(差异小于20%)。

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