Wickham Martin, Faulks Richard, Mills Clare
Institute of Food Research, Colney, Norwich NR4 7UA, UK.
Mol Nutr Food Res. 2009 Aug;53(8):952-8. doi: 10.1002/mnfr.200800193.
This article reviews the in vitro digestion models developed to assess the stability of food allergens during digestion. It is hypothesised that food allergens must exhibit sufficient gastro-intestinal stability to reach the intestinal mucosa where absorption and sensitisation (development of atopy) can occur. The investigation of stability of proteins within the gastrointestinal tract may provide prospective testing for allergenicity and could be a significant and valid parameter that distinguishes food allergens from nonallergens. Systematic evaluation of the stability of food allergens that are active via the gastrointestinal tract is currently tested in traditional pepsin digestibility models. The human gastrointestinal tract however is very complex and this article points out the importance of using physiologically relevant in vitro digestion systems for evaluating digestibility of allergens. This would involve the simulation of the stomach/small intestine environment (multi-phase models) with sequential addition of digestive enzymes, surfactants such as phospholipids and bile salts under physiological conditions, as well as the consideration of the effect of the food matrices on the allergen digestion.
本文综述了为评估食物过敏原在消化过程中的稳定性而开发的体外消化模型。据推测,食物过敏原必须表现出足够的胃肠道稳定性,才能到达肠道黏膜,在那里可能发生吸收和致敏(特应性的发展)。对胃肠道内蛋白质稳定性的研究可为致敏性提供前瞻性测试,并且可能是区分食物过敏原和非过敏原的一个重要且有效的参数。目前,在传统的胃蛋白酶消化率模型中测试通过胃肠道起作用的食物过敏原的稳定性。然而,人类胃肠道非常复杂,本文指出了使用生理相关的体外消化系统评估过敏原消化率的重要性。这将涉及在生理条件下模拟胃/小肠环境(多相模型),依次添加消化酶、表面活性剂如磷脂和胆汁盐,以及考虑食物基质对过敏原消化的影响。