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首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Allergic reactions to cyclophosphamide: delayed clinical expression associated with positive immediate skin tests to drug metabolites in five patients.
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Allergic reactions to cyclophosphamide: delayed clinical expression associated with positive immediate skin tests to drug metabolites in five patients.

机译:对环磷酰胺的过敏反应:5名患者对药物代谢物的即时皮肤试验阳性与延迟的临床表达有关。

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BACKGROUND: Cyclophosphamide (CP) is one of the relatively few drugs implicated in systemic allergic reactions for which the metabolites are well known. Formation of CP metabolites is a multistep, time-dependent process (hours) with significant interindividual differences. Although allergic reactions to CP have been recorded in 17 previous reports, skin testing with CP or its metabolites has been included in only five. We now describe five patients receiving monthly cycles of intravenous CP whose allergic reactions included clinical features of type I hypersensitivity but were atypical in their markedly delayed onset (i.e., 8 to 16 hours in patients 1 to 4 and 10 days in patient 5). OBJECTIVE: The objective was to investigate these late-developing clinical reactions by skin testing with CP and two of its major metabolites. METHODS: The five patients and a control group receiving intravenous CP uneventfully were studied by the same skin test protocol. RESULTS: The four individuals in the control group were unreactive to CP or its metabolites. All five patients with late-onset allergic reactions had positive immediate skin test results to CP metabolites but not to CP itself. We propose that the allergic reactions in patients 1 to 4 were mediated, wholly or in major part, by IgE antibodies reactive with allergens derived from time-dependent drug metabolites. The 10-day lag time in patient 5 is unexplained. Immunomodulation by the underlying malignancies or by the immunosuppressive drugs could have contributed. CONCLUSION: IgE-mediated allergic drug reactions may have a delayed onset if the allergen is a time-dependent drug metabolite, illustrated in this study by CP.
机译:背景:环磷酰胺(CP)是涉及代谢产物的全身性过敏反应的相对少数药物之一。 CP代谢产物的形成是一个多步骤的,时间依赖性的过程(小时),各个个体之间存在显着差异。尽管先前有17篇报道记录了对CP的过敏反应,但仅有5篇包含使用CP或其代谢物进行皮肤测试。我们现在描述五名每月接受静脉CP治疗的患者,他们的过敏反应包括I型超敏反应的临床特征,但起病时间明显不典型(例如,患者1至4的患者为8至16小时,患者5为10天)。目的:通过使用CP及其两种主要代谢产物进行皮肤测试来研究这些较晚发展的临床反应。方法:采用相同的皮肤测试方案对5名患者和对照组进行了静脉注射CP治疗。结果:对照组中的四个人对CP或其代谢产物无反应。所有五位迟发性过敏反应患者对CP代谢产物的即时皮肤测试结果均为阳性,而对CP本身则没有。我们建议,患者1至4的过敏反应全部或大部分由与源自时间依赖性药物代谢物的过敏原反应的IgE抗体介导。患者5的10天滞后时间无法解释。潜在的恶性肿瘤或免疫抑制药物引起的免疫调节可能有所贡献。结论:如果过敏原是时间依赖性药物代谢物,IgE介导的过敏性药物反应可能会延迟发作,CP在本研究中对此进行了说明。

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