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变应原结构与诊断之间的关联:了解你的表位。

Interfaces between allergen structure and diagnosis: know your epitopes.

作者信息

Pomés Anna, Chruszcz Maksymilian, Gustchina Alla, Wlodawer Alexander

机构信息

Basic Research, Indoor Biotechnologies, Inc., 1216 Harris Street, Charlottesville, VA, 22903, USA,

出版信息

Curr Allergy Asthma Rep. 2015 Apr;15(8):506. doi: 10.1007/s11882-014-0506-9.

Abstract

Allergy diagnosis is based on the patient's clinical history and can be strengthened by tests that confirm the origin of sensitization. In the past 25 years, these tests have evolved from the exclusive in vivo or in vitro use of allergen extracts, to complementary molecular-based diagnostics that rely on in vitro measurements of IgE reactivity to individual allergens. For this to occur, an increase in our understanding of the molecular structure of allergens, largely due to the development of technologies such as molecular cloning and expression of recombinant allergens, X-ray crystallography, or nuclear magnetic resonance (NMR), has been essential. New in vitro microarray or multiplex systems are now available to measure IgE against a selected panel of purified natural or recombinant allergens. The determination of the three-dimensional structure of allergens has facilitated detailed molecular studies, including the analysis of antigenic determinants for diagnostic purposes.

摘要

过敏诊断基于患者的临床病史,通过能确认致敏源的检测可得到加强。在过去25年里,这些检测已从单纯使用变应原提取物进行体内或体外检测,发展为基于分子的补充诊断方法,后者依靠体外测量IgE对单个变应原的反应性。为此,我们对变应原分子结构的理解有了提高,这在很大程度上得益于分子克隆和重组变应原表达、X射线晶体学或核磁共振(NMR)等技术的发展,这一点至关重要。现在有新的体外微阵列或多重检测系统可用于测量针对选定的一组纯化天然或重组变应原的IgE。变应原三维结构的确定有助于进行详细的分子研究,包括出于诊断目的对抗原决定簇的分析。

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