在新型食品蛋白的安全性测试中,是否应该用消化试验来评估潜在过敏原的持久性?

Q2 Medicine Clinical and Molecular Allergy Pub Date : 2009-01-15 DOI:10.1186/1476-7961-7-1
Santiago Schnell, Rod A Herman
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引用次数: 37

摘要

在西方发达国家,食物过敏影响了约3%至4%的成年人和高达8%的儿童。纯化蛋白质体外模拟胃消化研究的结果通常用于评估新型食物蛋白质的致敏潜力。纯化蛋白质在模拟胃液中的消化通常以指数方式进行,允许使用伪一阶速率常数或半衰期对持久性进行量化。然而,纯化蛋白在模拟胃液中的持续存在并不能很好地预测食物蛋白的致敏状态,这可能是由于食物基质在体内的显著影响。对暴露于模拟胃液中的整个制备食物中新型蛋白质的持久性的评估可能会提供更相关的结果,但在被接受用于预测新型食物蛋白质的致敏潜力之前,此类分析应经过彻底验证以证明其预测能力。
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Should digestion assays be used to estimate persistence of potential allergens in tests for safety of novel food proteins?

Food allergies affect an estimated 3 to 4% of adults and up to 8% of children in developed western countries. Results from in vitro simulated gastric digestion studies with purified proteins are routinely used to assess the allergenic potential of novel food proteins. The digestion of purified proteins in simulated gastric fluid typically progresses in an exponential fashion allowing persistence to be quantified using pseudo-first-order rate constants or half lives. However, the persistence of purified proteins in simulated gastric fluid is a poor predictor of the allergenic status of food proteins, potentially due to food matrix effects that can be significant in vivo. The evaluation of the persistence of novel proteins in whole, prepared food exposed to simulated gastric fluid may provide a more correlative result, but such assays should be thoroughly validated to demonstrate a predictive capacity before they are accepted to predict the allergenic potential of novel food proteins.

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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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