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首页> 外文期刊>HNO >Microarray technique for component resolved diagnosis (CRD) in type-I allergies. An innovative technology at the border between research tool and routine diagnostics
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Microarray technique for component resolved diagnosis (CRD) in type-I allergies. An innovative technology at the border between research tool and routine diagnostics

机译:用于I型过敏的成分分辨诊断(CRD)的微阵列技术。研究工具和常规诊断之间的边界的创新技术

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摘要

Approximately 25% of the population in industrialized countries suffer from IgE-associated Type-1 allergies. Multiple allergens can be tested simultaneously in one assay by using the protein microarray. Moreover, it is possible to measure more than one analytical parameter (e.g. allergen specific IgEs and IgGs) in one assay by combining different fluorescent markers with specific secondary antibodies. The different allergen components that are of interest are immobilized on a planar surface. By adding the patient's serum (a smaller amount of serum is needed compared to an immunoassay) the inherent IgE antibodies are captured by the corresponding allergens. Secondary fluorescing anti-IgE antibodies are added subsequently, thus the intensity of each spot on the microarray can be measured by using a biochipscanner. The detected signal is then transformed into quantitative data, which allows the classification of the patient's serum IgE level for the tested allergens. There are different approaches to reduce the complexity of the original extracts used for the production of the solid microarray phase to a smaller number of relevant pathogenic molecules. The component-resolved diagnosis still needs to be clinically validated, but initial studies show positive results concerning the sensitivity and specificity of the protein microarray. Protein microarrays are promising tools for screening diagnoses in allergic diseases as well as for the improvement of allergen-specific immunotherapy.
机译:在工业化国家中,大约25%的人口患有与IgE相关的1型过敏。可以使用蛋白质微阵列在一种测定法中同时检测多种过敏原。此外,通过将不同的荧光标记物与特异性二抗结合,可以在一种测定中测量一种以上的分析参数(例如,变应原特异性IgE和IgG)。感兴趣的不同变应原成分固定在平面上。通过添加患者的血清(与免疫测定相比,需要的血清量更少),固有的IgE抗体会被相应的过敏原捕获。随后添加二抗荧光抗IgE抗体,因此可以使用生物芯片扫描仪测量微阵列上每个斑点的强度。然后将检测到的信号转换为定量数据,从而可以对所测试的过敏原对患者的血清IgE水平进行分类。有不同的方法可以将用于生产固体微阵列相的原始提取物的复杂性降低为较少数量的相关致病分子。成分分辨的诊断仍需临床验证,但初步研究显示有关蛋白质微阵列敏感性和特异性的积极结果。蛋白质微阵列是用于筛选过敏性疾病诊断以及改善过敏原特异性免疫疗法的有前途的工具。

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