Allergen Microarrays and New Physical Approaches to More Sensitive and Specific Detection of Allergen-Specific Antibodies

Biosensors Pub Date : 2024-07-20 DOI:10.3390/bios14070353
Pavel Sokolov, Irina Evsegneeva, Alexander Karaulov, Alyona Sukhanova, Igor Nabiev
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Abstract

The prevalence of allergic diseases has increased tremendously in recent decades, which can be attributed to growing exposure to environmental triggers, changes in dietary habits, comorbidity, and the increased use of medications. In this context, the multiplexed diagnosis of sensitization to various allergens and the monitoring of the effectiveness of treatments for allergic diseases become particularly urgent issues. The detection of allergen-specific antibodies, in particular, sIgE and sIgG, is a modern alternative to skin tests due to the safety and efficiency of this method. The use of allergen microarrays to detect tens to hundreds of allergen-specific antibodies in less than 0.1 mL of blood serum enables the transition to a deeply personalized approach in the diagnosis of these diseases while reducing the invasiveness and increasing the informativeness of analysis. This review discusses the technological approaches underlying the development of allergen microarrays and other protein microarrays, including the methods of selection of the microarray substrates and matrices for protein molecule immobilization, the obtainment of allergens, and the use of different types of optical labels for increasing the sensitivity and specificity of the detection of allergen-specific antibodies.
过敏原微阵列和新的物理方法,更灵敏、更特异地检测过敏原特异性抗体
近几十年来,过敏性疾病的发病率急剧上升,其原因包括接触环境诱因的机会越来越多、饮食习惯的改变、合并症以及药物使用的增加。在这种情况下,对各种过敏原的过敏性进行多重诊断以及监测过敏性疾病的治疗效果就成了尤为紧迫的问题。检测过敏原特异性抗体,特别是 sIgE 和 sIgG,因其安全高效而成为皮试的现代替代方法。使用过敏原微阵列可在不到 0.1 毫升的血清中检测数十种至数百种过敏原特异性抗体,从而在诊断这些疾病时过渡到深度个性化的方法,同时降低侵入性并增加分析的信息量。本综述讨论了开发过敏原芯片和其他蛋白质芯片的基本技术方法,包括芯片基底和蛋白质分子固定基质的选择方法、过敏原的获取以及使用不同类型的光学标签来提高过敏原特异性抗体检测的灵敏度和特异性。
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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