CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS)/ Service de Pharmacologie et d'Immunoanalyse, Université Paris-Saclay, Gif-sur-Yvette, France.
Section of Inflammation, Repair & Development, National Heart & Lung Institute, Imperial College London, London, UK.
Clin Exp Allergy. 2020 Sep;50(9):1093-1102. doi: 10.1111/cea.13706. Epub 2020 Jul 27.
Bioaccessibility of food allergens may be a key determinant of allergic reactions.
To develop a protocol allowing the detection of the major peanut allergen, Ara h 6, in the bloodstream following ingestion of low amounts of peanut and to compare Ara h 6 bioaccessibility by food matrix. We further assessed for differences in absorption in healthy versus peanut-allergic volunteers.
A blood pretreatment combining acidic shock and thermal treatment was developed. This protocol was then applied to blood samples collected from human volunteers (n = 6, healthy controls; n = 14, peanut-allergic patients) at various time-points following ingestion of increasing levels of peanut incurred in different food matrices (cookies, peanut butter and chocolate dessert). Immunodetection was performed using an in-house immunoassay.
An original pretreatment protocol was optimized, resulting in irreversible dissociation of human antibodies-Ara h 6 immune complex, thus rendering Ara h 6 accessible for its immunodetection. Ara h 6 was detected in samples from all volunteers following ingestion of 300-1000 mg peanut protein, although variations in the kinetics of passage were observed between individuals and matrices. Interestingly, in peanut-allergic subjects, Ara h 6 could be detected following ingestion of lower doses and at higher concentrations than in non-allergic volunteers.
The kinetics and intensity of Ara h 6 passage in bloodstream depend on both individual and food matrix. Peanut-allergic patients appear to demonstrate higher absorption rate, the clinical significance of which warrants further evaluation.
食物过敏原的生物可及性可能是过敏反应的关键决定因素。
开发一种方案,允许在摄入少量花生后检测血液中的主要花生过敏原 Ara h 6,并比较不同食物基质中 Ara h 6 的生物可及性。我们进一步评估了健康志愿者和花生过敏志愿者之间吸收的差异。
开发了一种血液预处理方法,结合酸性冲击和热处理。然后将该方案应用于从摄入不同食物基质(饼干、花生酱和巧克力甜点)中增加的花生水平后不同时间点采集的人类志愿者(n=6,健康对照;n=14,花生过敏患者)的血液样本。使用内部免疫测定法进行免疫检测。
优化了原始预处理方案,导致人抗体-Ara h 6 免疫复合物不可逆解离,从而使 Ara h 6 可用于免疫检测。在摄入 300-1000mg 花生蛋白后,所有志愿者的样本中均检测到 Ara h 6,尽管个体和基质之间的通过动力学存在差异。有趣的是,在花生过敏患者中,摄入较低剂量和较高浓度的 Ara h 6 后即可检测到。
Ara h 6 在血液中的通过动力学和强度取决于个体和食物基质。花生过敏患者似乎表现出更高的吸收率,其临床意义值得进一步评估。