Department of Pathophysiology, Medical University of Vienna, Vienna, Austria.
Clin Exp Allergy. 2010 Mar;40(3):486-93. doi: 10.1111/j.1365-2222.2009.03363.x. Epub 2009 Oct 7.
Hypersensitivity reactions towards non-steroidal anti-inflammatory drugs (NSAID) are common, although true allergies are detectable only in a subgroup of patients. The current study was prompted by a case observation, where a patient experienced generalized urticaria following his second course of diclofenac and proton pump inhibitor medication, and was found to have diclofenac-specific IgE. During recent years, our group has been investigating the importance of gastric digestion in the development of food allergies, demonstrating anti-acid medication as a risk factor for sensitization against food proteins.
Here, we aimed to investigate whether the mechanism of food allergy induction described can also be causative in NSAID allergy, using diclofenac as a paradigm.
We subjected BALB/c mice to several oral immunization regimens modelled after the patient's medication intake. Diclofenac was applied with or without gastric acid suppression, in various doses, alone or covalently coupled to albumin, a protein abundant in gastric juices. Immune responses were assessed on the antibody level, and functionally examined by in vitro and in vivo crosslinking assays.
Only mice receiving albumin-coupled diclofenac under gastric acid suppression developed anti-diclofenac IgG1 and IgE, whereas no immune responses were induced by the drug alone or without gastric acid suppression. Antibody induction was dose dependent with the group receiving the higher dose of the drug showing sustained anti-diclofenac titres. The antibodies induced triggered basophil degranulation in vitro and positive skin tests in vivo.
Gastric acid suppression was found to be a causative mechanism in the induction of IgE-mediated diclofenac allergy.
非甾体抗炎药(NSAID)过敏反应很常见,尽管真正的过敏反应仅在一小部分患者中可检测到。本研究是由一例病例观察引发的,该患者在第二次使用双氯芬酸和质子泵抑制剂药物后出现全身性荨麻疹,并且发现对双氯芬酸具有特异性 IgE。近年来,我们的研究小组一直在研究胃消化在食物过敏发展中的重要性,证明抗酸药物是对食物蛋白致敏的危险因素。
本研究旨在探讨我们描述的食物过敏诱导机制是否也与 NSAID 过敏有关,以双氯芬酸为例。
我们对 BALB/c 小鼠进行了几种口服免疫方案,模拟了患者的药物摄入情况。双氯芬酸与或不与胃酸抑制一起应用,剂量不同,单独或与白蛋白共价偶联,白蛋白是胃中丰富的蛋白质。在抗体水平上评估免疫反应,并通过体外和体内交联测定来功能检查。
只有在胃酸抑制下接受白蛋白偶联双氯芬酸的小鼠才会产生抗双氯芬酸 IgG1 和 IgE,而单独使用药物或没有胃酸抑制则不会引起免疫反应。抗体诱导与剂量有关,接受较高剂量药物的组显示持续的抗双氯芬酸效价。诱导的抗体在体外引发嗜碱性粒细胞脱颗粒,并在体内引发阳性皮肤试验。
胃酸抑制被发现是 IgE 介导的双氯芬酸过敏诱导的一个致病机制。