High frequency of IgE sensitization towards kiwi seed storage proteins among peanut allergic individuals also reporting allergy to kiwi.

Q2 Medicine
Clinical and Molecular Allergy Pub Date : 2017-11-01 eCollection Date: 2017-01-01 DOI:10.1186/s12948-017-0073-4
Jenny van Odijk, Sigrid Sjölander, Peter Brostedt, Magnus P Borres, Hillevi Englund
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引用次数: 7

Abstract

Background: IgE sensitization to storage proteins from nuts and seed is often related to severe allergic symptoms. There is a risk of immunological IgE cross-reactivity between storage proteins from different species. The potential clinical implication of such cross-reactivity is that allergens other than the known sensitizer can cause allergic symptoms. Previous studies have suggested that kiwi seed storage proteins may constitute hidden food allergens causing cross-reactive IgE-binding with peanut and other tree nut homologs, thereby mediating a potential risk of causing allergy symptoms among peanut ant tree nut allergic individuals. The objective of this study was to investigate the degree of sensitization towards kiwi fruit seed storage proteins in a cohort of peanut allergic individuals.

Methods: A cohort of 59 adolescents and adults with peanut allergy was studied, and self reported allergies to a number of additional foods were collected. Quantitative IgE measurements to seed storage proteins from kiwi and peanut were performed.

Results: In the cohort, 23 out of the 59 individuals were reporting kiwi fruit allergy (39%). The frequency of IgE sensitization to kiwi fruit and to any kiwi seed storage protein was higher among peanut allergic individuals also reporting kiwi fruit allergy (P = 0.0001 and P = 0.01). A positive relationship was found between IgE levels to 11S globulin (r = 0.65) and 7S globulin (r = 0.48) allergens from kiwi and peanut, but IgE levels to 2S albumin homologs did not correlate. Patients reporting kiwi fruit allergy also reported allergy to hazelnut (P = 0.015), soy (P < 0.0001), pea (P = 0.0002) and almond (P = 0.016) to a higher extent than peanut allergic individuals without kiwi allergy.

Conclusions: Thirty-nine percent of the peanut allergic patients in this cohort also reported kiwi fruit allergy, they displayed a higher degree of sensitization to kiwi storage proteins from both kiwi and peanut, and they also reported a higher extent of allergy to other nuts and legumes. On the molecular level, there was a correlation between IgE levels to 11S and 7S storage proteins from kiwi and peanut. Taken together, reported symptoms and serological findings to kiwi in this cohort of patients with concurrent allergy to peanut and kiwi fruit, could be explained by a combination of cross-reactivity between the 11S and 7S globulins and co-sensitization to the 2S albumin Act d 13.

Abstract Image

在花生过敏个体中,对猕猴桃种子储存蛋白的高频率IgE敏化也报告了对猕猴桃的过敏。
背景:对坚果和种子储存蛋白的IgE致敏通常与严重的过敏症状有关。不同种类的储存蛋白之间存在免疫IgE交叉反应的风险。这种交叉反应的潜在临床意义是,除已知的致敏剂外,其他过敏原也可引起过敏症状。先前的研究表明,猕猴桃种子储存蛋白可能构成隐藏的食物过敏原,与花生和其他树坚果同源物产生交叉反应性ige结合,从而介导花生蚂蚁树坚果过敏个体的过敏症状的潜在风险。本研究的目的是调查一组花生过敏个体对猕猴桃种子储存蛋白的致敏程度。方法:对59名花生过敏的青少年和成人进行了研究,并收集了对一些其他食物的自我过敏报告。对猕猴桃和花生的种子贮藏蛋白进行了定量的IgE测定。结果:在队列中,59个人中有23人报告猕猴桃过敏(39%)。报告猕猴桃过敏的花生过敏个体对猕猴桃和任何猕猴桃种子储存蛋白的IgE致敏频率更高(P = 0.0001和P = 0.01)。猕猴桃和花生中11S球蛋白(r = 0.65)和7S球蛋白(r = 0.48)与IgE水平呈正相关,而与2S白蛋白同源物的IgE水平不相关。报告猕猴桃过敏的患者对榛子(P = 0.015)、大豆(P = 0.0002)和杏仁(P = 0.016)的过敏程度也高于没有猕猴桃过敏的花生过敏者。结论:在这个队列中,39%的花生过敏患者也报告了猕猴桃过敏,他们对猕猴桃和花生中的猕猴桃储存蛋白表现出更高程度的过敏,他们也报告了对其他坚果和豆类的更高程度的过敏。在分子水平上,IgE水平与猕猴桃和花生的11S和7S贮藏蛋白存在相关性。综上所述,在这组同时对花生和猕猴桃过敏的患者中,报告的症状和对猕猴桃的血清学结果可以用11S和7S球蛋白之间的交叉反应以及对2S白蛋白Act 13的共同敏化来解释。
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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来源期刊
Clinical and Molecular Allergy
Clinical and Molecular Allergy Medicine-Immunology and Allergy
CiteScore
8.20
自引率
0.00%
发文量
11
审稿时长
13 weeks
期刊介绍: Clinical and Molecular Allergy is an open access, peer-reviewed, online journal that publishes research on human allergic and immunodeficient disease (immune deficiency not related to HIV infection/AIDS). The scope of the journal encompasses all aspects of the clinical, genetic, molecular and inflammatory aspects of allergic-respiratory (Type 1 hypersensitivity) and non-AIDS immunodeficiency disorders. However, studies of allergic/hypersensitive aspects of HIV infection/AIDS or drug desensitization protocols in AIDS are acceptable. At the basic science level, this includes original work and reviews on the genetic and molecular mechanisms underlying the inflammatory response.
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