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通过流式细胞术和扫描电子显微镜对免疫球蛋白G(IgG)与霉菌孢子结合进行定量和表征。

Quantification and characterisation of IgG binding to mould spores by flow cytometry and scanning electron microscopy.

作者信息

Rydjord Britt, Namork Ellen, Nygaard Unni Cecilie, Wiker Harald G, Hetland Geir

机构信息

Department of Environmental Immunology, Norwegian Institute of Public Health, Oslo, Norway.

出版信息

J Immunol Methods. 2007 Jun 30;323(2):123-31. doi: 10.1016/j.jim.2007.04.001. Epub 2007 Apr 27.

DOI:10.1016/j.jim.2007.04.001
PMID:17490674
Abstract

The concentration of mould-specific IgG antibodies in serum may objectively indicate mould exposure and can help identifying exposed individuals. Although inhaled spores probably are the most important source of mould exposure, the commonly used methods for detecting mould-specific IgG antibodies are based on extracts from all mould components, with only low contribution from spores. We have developed a flow cytometric method using surface antigens on mould spores for quantifying mould-specific IgG antibodies in serum. Flow cytometric results were evaluated by comparison with ImmunoCap and ELISA measurements. The flow cytometric assay showed a broad linear dose-dependency and correlated moderately to strongly (r=0.41-0.97) with ImmunoCap and ELISA measurements. The IgG antibody binding was studied in detail by immunolabelling in scanning electron microscopy (SEM), revealing that morphology and IgG antibody binding differed among spores, both within and between mould strains. Germination studies by flow cytometry and SEM showed that IgG antibody binding to mould spores was altered during germination due to loss of coat. The present spore based antibody assay are simple and suitable for quantification of mould-specific IgG antibodies in serum, and includes specificity to other and possibly more relevant antigens than existing methods.

摘要

血清中霉菌特异性IgG抗体的浓度可客观地表明霉菌暴露情况,并有助于识别暴露个体。尽管吸入的孢子可能是霉菌暴露的最重要来源,但常用的检测霉菌特异性IgG抗体的方法是基于所有霉菌成分的提取物,孢子的贡献很低。我们开发了一种流式细胞术方法,利用霉菌孢子表面抗原定量血清中的霉菌特异性IgG抗体。通过与免疫捕获法和酶联免疫吸附测定法的测量结果进行比较,对流式细胞术结果进行评估。流式细胞术检测显示出广泛的线性剂量依赖性,与免疫捕获法和酶联免疫吸附测定法的测量结果中度至高度相关(r=0.41-0.97)。通过扫描电子显微镜(SEM)免疫标记详细研究了IgG抗体结合情况,结果表明,在霉菌菌株内部和之间,孢子的形态和IgG抗体结合情况存在差异。通过流式细胞术和SEM进行的萌发研究表明,由于外壳丢失,萌发过程中IgG抗体与霉菌孢子的结合发生了改变。目前基于孢子的抗体检测方法简单,适用于定量血清中的霉菌特异性IgG抗体,并且比现有方法对其他可能更相关的抗原有更高的特异性。

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