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过敏致敏:筛选方法。

Allergic sensitization: screening methods.

机构信息

DuPont Pioneer Agricultural Biotechnology, DuPont Experimental Station, 200 Powder Mill Road, Wilmington, DE 19880-0400, USA.

出版信息

Clin Transl Allergy. 2014 Apr 15;4(1):13. doi: 10.1186/2045-7022-4-13.

Abstract

Experimental in silico, in vitro, and rodent models for screening and predicting protein sensitizing potential are discussed, including whether there is evidence of new sensitizations and allergies since the introduction of genetically modified crops in 1996, the importance of linear versus conformational epitopes, and protein families that become allergens. Some common challenges for predicting protein sensitization are addressed: (a) exposure routes; (b) frequency and dose of exposure; (c) dose-response relationships; (d) role of digestion, food processing, and the food matrix; (e) role of infection; (f) role of the gut microbiota; (g) influence of the structure and physicochemical properties of the protein; and (h) the genetic background and physiology of consumers. The consensus view is that sensitization screening models are not yet validated to definitively predict the de novo sensitizing potential of a novel protein. However, they would be extremely useful in the discovery and research phases of understanding the mechanisms of food allergy development, and may prove fruitful to provide information regarding potential allergenicity risk assessment of future products on a case by case basis. These data and findings were presented at a 2012 international symposium in Prague organized by the Protein Allergenicity Technical Committee of the International Life Sciences Institute's Health and Environmental Sciences Institute.

摘要

讨论了用于筛选和预测蛋白质致敏潜力的实验性计算机模拟、体外和啮齿动物模型,包括自 1996 年转基因作物引入以来是否有新的致敏和过敏证据、线性与构象表位的重要性,以及成为过敏原的蛋白质家族。还解决了一些预测蛋白质致敏的常见挑战:(a) 暴露途径;(b) 暴露的频率和剂量;(c) 剂量-反应关系;(d) 消化、食品加工和食品基质的作用;(e) 感染的作用;(f) 肠道微生物群的作用;(g) 蛋白质结构和物理化学性质的影响;以及 (h) 消费者的遗传背景和生理学。共识是,致敏筛选模型尚未经过验证,无法明确预测新型蛋白质的从头致敏潜力。然而,它们在了解食物过敏发展机制的发现和研究阶段将非常有用,并且可能会提供有关未来产品潜在致敏性风险评估的信息,这是一个具体问题具体分析的情况。这些数据和发现是在 2012 年由国际生命科学研究所健康与环境科学研究所的蛋白质变应原性技术委员会在布拉格组织的一次国际研讨会上提出的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e54/3990213/2248436a9e9f/2045-7022-4-13-1.jpg

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