Bacarese-Hamilton Tito, Gray Julian, Ardizzoni Andrea, Crisanti Andrea
Department of Biological Sciences, Imperial College London, London, UK.
Methods Mol Med. 2005;114:195-207. doi: 10.1385/1-59259-923-0:195.
Allergy affects more than 25% of Western populations (1) and is estimated to be the sixth leading cause of chronic disease in the United States and Western Europe. The complexity of the condition is such that hundreds of common allergens have been described, and in order to maximize diagnostic efficiency there is an urgent clinical requirement for assays to provide multiple-allergen determination in a timely and cost-effective manner. Miniaturized immunoassays that utilize protein microarray technology now offer the possibility of circumventing most of the current limitations in the serodiagnosis of allergic disease. The heterogeneous nature of allergens presents many challenges in all aspects of developing such arrays, from immobilization of the capture molecule to detection of the bound ligand. In addition, there is no simple method of protein amplification (such as PCR for nucleic acids), and stabilization is yet a further major consideration. Notwithstanding these challenges, protein microarrays have been developed for the serodiagnosis of allergies and other complex clinical conditions. These assays exhibit good analytical and clinical performance and deliver significant advantages in convenience and cost compared with traditional ELISA test formats. This chapter details the techniques employed in the construction and processing of an allergen array specific for the serodiagnosis of allergic disease. An overview of protein microarray technology is provided and the principles that underpin the suitability for use of this technology in the identification and measurement of particular proteins in patient sera (serum profiling) are discussed.
过敏影响超过25%的西方人群(1),据估计在美国和西欧是慢性病的第六大主要病因。该病症十分复杂,已描述的常见过敏原达数百种,为了最大程度提高诊断效率,临床上迫切需要能及时且经济高效地进行多种过敏原检测的分析方法。利用蛋白质微阵列技术的小型化免疫分析现在提供了规避过敏性疾病血清诊断中当前大多数限制的可能性。过敏原的异质性在开发此类阵列的各个方面都带来了许多挑战,从捕获分子的固定到结合配体的检测。此外,不存在简单的蛋白质扩增方法(如用于核酸的PCR),稳定性也是另一个主要考虑因素。尽管存在这些挑战,但已开发出用于过敏和其他复杂临床病症血清诊断的蛋白质微阵列。这些分析方法具有良好的分析和临床性能,与传统酶联免疫吸附测定(ELISA)测试形式相比,在便利性和成本方面具有显著优势。本章详细介绍了用于构建和处理针对过敏性疾病血清诊断的过敏原阵列所采用的技术。提供了蛋白质微阵列技术的概述,并讨论了支持该技术适用于识别和测量患者血清中特定蛋白质(血清分析)的原理。