{"title":"抗体亲和力测定在变态反应诊断中的应用","authors":"G. Lain","doi":"10.5281/ZENODO.31285","DOIUrl":null,"url":null,"abstract":"u SPRi allows a multiplex monitoring of the complex antibody response to the major allergens of an allergenic source u SPRi monitoring is faster, label-free and more informative than ELISA, but less sensitive u The avidity of the antibody response may be evaluated and this evaluation is reproducible Conclusion The biological diagnosis of type I hypersensitivity reactions is based on the quantification of specific IgEs. However, the IgE titer is not always strongly related to the clinical symptoms or predictive of the evolution of the disease. The specificity and affinity of antibodies of other isotypes may contribute to the allergic status of the patients. The aim of this work was to develop a method that simultaneously detects the complex antibody response to various allergens and measures the avidity of the antibodies directed to each allergen (Cf Journal of immunological Methods, Volume 405, March 2014, Pages 23–28). We developed a tool to detect and measure the avidity of the various antibodies recognizing the major allergens of an allergenic source. Surface Plasmon Resonance imaging (SPRi) is a sensitive label-free method to detect and visualize biomolecular interactions. Our configuration allows the use of a pattern of various immobilized molecules and simultaneously follows up the kinetic curves of each spotted molecule. Introduction","PeriodicalId":315352,"journal":{"name":"Basel Life Science Week","volume":"256 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2015-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Affinity Measurement of Antibodies in Allergy Diagnosis\",\"authors\":\"G. Lain\",\"doi\":\"10.5281/ZENODO.31285\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"u SPRi allows a multiplex monitoring of the complex antibody response to the major allergens of an allergenic source u SPRi monitoring is faster, label-free and more informative than ELISA, but less sensitive u The avidity of the antibody response may be evaluated and this evaluation is reproducible Conclusion The biological diagnosis of type I hypersensitivity reactions is based on the quantification of specific IgEs. However, the IgE titer is not always strongly related to the clinical symptoms or predictive of the evolution of the disease. The specificity and affinity of antibodies of other isotypes may contribute to the allergic status of the patients. The aim of this work was to develop a method that simultaneously detects the complex antibody response to various allergens and measures the avidity of the antibodies directed to each allergen (Cf Journal of immunological Methods, Volume 405, March 2014, Pages 23–28). We developed a tool to detect and measure the avidity of the various antibodies recognizing the major allergens of an allergenic source. Surface Plasmon Resonance imaging (SPRi) is a sensitive label-free method to detect and visualize biomolecular interactions. Our configuration allows the use of a pattern of various immobilized molecules and simultaneously follows up the kinetic curves of each spotted molecule. Introduction\",\"PeriodicalId\":315352,\"journal\":{\"name\":\"Basel Life Science Week\",\"volume\":\"256 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-09-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Basel Life Science Week\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5281/ZENODO.31285\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Basel Life Science Week","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5281/ZENODO.31285","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
与ELISA相比,SPRi监测速度更快,无标记,信息量更大,但灵敏度较低。可对抗体反应的快速性进行评估,且该评估具有可重复性。结论1型超敏反应的生物学诊断是基于特异性IgEs的定量。然而,IgE滴度并不总是与临床症状或预测疾病的发展密切相关。其他同型抗体的特异性和亲和力可能与患者的过敏状态有关。这项工作的目的是开发一种方法,可以同时检测对各种过敏原的复杂抗体反应,并测量针对每种过敏原的抗体的亲和力(Cf Journal of immunological Methods, Volume 405, March 2014, Pages 23-28)。我们开发了一种工具来检测和测量识别过敏原来源的主要过敏原的各种抗体的贪婪度。表面等离子体共振成像(SPRi)是一种灵敏的无标记检测和可视化生物分子相互作用的方法。我们的配置允许使用各种固定分子的模式,并同时跟踪每个斑点分子的动力学曲线。介绍
Affinity Measurement of Antibodies in Allergy Diagnosis
u SPRi allows a multiplex monitoring of the complex antibody response to the major allergens of an allergenic source u SPRi monitoring is faster, label-free and more informative than ELISA, but less sensitive u The avidity of the antibody response may be evaluated and this evaluation is reproducible Conclusion The biological diagnosis of type I hypersensitivity reactions is based on the quantification of specific IgEs. However, the IgE titer is not always strongly related to the clinical symptoms or predictive of the evolution of the disease. The specificity and affinity of antibodies of other isotypes may contribute to the allergic status of the patients. The aim of this work was to develop a method that simultaneously detects the complex antibody response to various allergens and measures the avidity of the antibodies directed to each allergen (Cf Journal of immunological Methods, Volume 405, March 2014, Pages 23–28). We developed a tool to detect and measure the avidity of the various antibodies recognizing the major allergens of an allergenic source. Surface Plasmon Resonance imaging (SPRi) is a sensitive label-free method to detect and visualize biomolecular interactions. Our configuration allows the use of a pattern of various immobilized molecules and simultaneously follows up the kinetic curves of each spotted molecule. Introduction