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抑酸治疗与过敏反应。

Acid suppression therapy and allergic reactions.

作者信息

Untersmayr Eva

机构信息

Department of Pathophysiology and Allergy Research, Center of Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.

出版信息

Allergo J Int. 2015 Dec;24(8):303-311. doi: 10.1007/s40629-015-0085-x.

Abstract

The development of pharmaceutical agents such as sucralfate, histamine 2 (H2) receptor blockers and proton pump inhibitors (PPIs) reducing gastric acidity has been a mile stone for treatment of dyspeptic disorders. However, due to current prescription habits resulting in overuse of these potent drugs as well as over-the-counter (OTC) availability associated with self-medication, substantial health concern is related to the mechanisms of drug action as well as known side effects influencing gastrointestinal physiology. More than a decade ago the first study appeared reporting an association between anti-ulcer drug intake and food allergy development. Ever since this first report several experimental as well as human studies verified this correlation, demonstrating that acid suppressive drugs not only influence the sensitization capacity of orally ingested proteins, but also represent a risk factor for food allergy patients. Additionally, gastric acid suppression was reported to increase the risk for development of drug hypersensitivity reactions. These consequences of anti-ulcer drug intake might on the one hand be associated with direct influence of these drugs on immune responses. On the other hand reduction of gastric acidity leads to impaired gastrointestinal protein degradation. Nevertheless, also disruption of the gastrointestinal barrier function, changes in microbiome or lack of tolerogenic peptic digests might contribute to the connection between anti-ulcer drug intake and allergic reaction. Therefore, these drugs should only be prescribed based on a precise gastroenterological diagnosis taking into consideration allergological mechanisms to ensure patients' safety.

摘要

诸如硫糖铝、组胺2(H2)受体阻滞剂和质子泵抑制剂(PPI)等降低胃酸的药物的开发,是治疗消化不良疾病的一个里程碑。然而,由于目前的处方习惯导致这些强效药物的过度使用,以及与自我用药相关的非处方(OTC)可用性,人们对药物作用机制以及影响胃肠生理学的已知副作用存在重大健康担忧。十多年前,第一项研究报道了服用抗溃疡药物与食物过敏发生之间的关联。自该首次报告以来,多项实验研究和人体研究证实了这种相关性,表明抑酸药物不仅会影响口服蛋白质的致敏能力,而且也是食物过敏患者的一个风险因素。此外,据报道胃酸抑制会增加药物过敏反应发生的风险。服用抗溃疡药物的这些后果一方面可能与这些药物对免疫反应的直接影响有关。另一方面,胃酸减少会导致胃肠蛋白质降解受损。然而,胃肠屏障功能的破坏、微生物群的变化或缺乏耐受性消化产物也可能导致服用抗溃疡药物与过敏反应之间的联系。因此,这些药物仅应在精确的胃肠病学诊断基础上开具处方,并考虑过敏机制以确保患者安全。

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