Determination of Crucial Immunogenic Epitopes in Major Peanut Allergy Protein, Ara h2, via Novel Nanoallergen Platform

被引:17
作者
Deak, Peter E. [1 ]
Vrabel, Maura R. [1 ]
Kiziltepe, Tanyel [1 ,2 ]
Bilgicer, Basar [1 ,2 ,3 ]
机构
[1] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Adv Diagnost & Therapeut, Notre Dame, IN 46556 USA
[3] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
基金
美国国家科学基金会;
关键词
FC-EPSILON-RI; SYNTHETIC ALLERGEN; CROSS-REACTIVITY; CELLULAR UPTAKE; IGE EPITOPES; FOOD ALLERGY; MAST-CELLS; AFFINITY; REVEALS; DESIGN;
D O I
10.1038/s41598-017-04268-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Current methods for detection and diagnosis of allergies do not provide epitope specific immunogenic information and hence lack critical information that could aid in the prediction of clinical responses. To address this issue, we developed a nanoparticle based platform, called nanoallergens that enable multivalent display of potential allergy epitopes for determining the immunogenicity of each IgE binding epitope. By synthesizing nanoallergens that present various epitopes from the major peanut allergen, Ara h2, we directly determined the immunogenicity of each epitope, alone and in combination with other epitopes, using patient sera. This information provided insights on which epitopes are most critical for physiological responses to Ara h2 and revealed the importance of both high and low affinity epitopes for allergic responses. We anticipate the nanoallergen platform to be used to provide information regarding allergic reactions and therefore potentially aid in more accurate diagnosis and design of personalized treatment options.
引用
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页数:13
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