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非甾体抗炎药过敏反应。

Hypersensitivity reactions to non-steroidal anti-inflammatory drugs.

机构信息

Research Group of Allergic Diseases, Research Laboratory, IMABIS Foundation-Carlos Haya Hospital, Málaga, Spain.

出版信息

Curr Drug Metab. 2009 Nov;10(9):971-80. doi: 10.2174/138920009790711841.

Abstract

NSAIDs are the most important group of drugs involved in hypersensitivity drug reactions, and include heterogeneous compounds with very different chemical structures. These reactions can be IgE dependent (immediate reactions), T cell-mediated (non-immediate), or induced by a non-specific immunological mechanism related with the blocking of the COX-1 enzyme and the shunting to the lipooxygenase pathway (cross-intolerant reactions). Cutaneous symptoms are the most frequent, with ibuprofen, naproxen and diclofenac being common culprit drugs worldwide, although others can be involved because patterns of consumption and exposure rates vary between countries. A very important proportion of immunological reactions are immediate, with urticaria and anaphylaxis being the typical clinical manifestations. Non-immediate reactions comprise a number of heterogeneous entities ranging from mild exanthema to severe TEN or DRESS syndrome, as well as organ-specific reactions such as hepatitis or pneumonitis. Cross-intolerant reactions appear to non-chemically related drugs, and involve respiratory airways, skin or both. In vivo diagnostic tests are based on the capacity of the skin to respond to the culprit drug, but their sensitivity is in many instances rather low. The approach for in vitro testing consists of either detecting specific IgE antibodies or studying the proliferation of T lymphocytes toward the eliciting drug. No appropriate tests are yet available for the in vitro validation of cross-intolerance reactions, although techniques based on the stimulation of basophils have been proposed. Based on these findings, the diagnostic approach is often based on the controlled administration of the drug to assess tolerance. In this work we review current knowledge on hypersensitivity reactions to NSAIDs, including diagnostic approach and genetic studies.

摘要

非甾体抗炎药(NSAIDs)是引起药物超敏反应最重要的一组药物,包括具有非常不同化学结构的异质化合物。这些反应可以是 IgE 依赖性(即刻反应)、T 细胞介导的(非即刻反应),也可以是非特异性免疫机制诱导的,与 COX-1 酶的阻断和向脂氧合酶途径转移有关(交叉耐受反应)。皮肤症状是最常见的,布洛芬、萘普生和双氯芬酸是全球常见的罪魁祸首药物,尽管其他药物也可能涉及,因为各国的消费模式和暴露率不同。相当一部分免疫反应是即刻的,其典型临床表现为荨麻疹和过敏反应。非即刻反应包括一系列异质实体,从轻度出疹到严重的史蒂文斯-约翰逊综合征(SJS)或中毒性表皮坏死松解症(TEN),以及肝、肺等器官特异性反应。交叉耐受反应似乎与非化学相关的药物有关,涉及呼吸道、皮肤或两者。体内诊断测试基于皮肤对罪魁祸首药物的反应能力,但在许多情况下其敏感性相当低。体外测试方法包括检测特异性 IgE 抗体或研究 T 淋巴细胞对诱发药物的增殖。目前还没有用于体外验证交叉耐受反应的合适测试方法,尽管已经提出了基于刺激嗜碱性粒细胞的技术。基于这些发现,诊断方法通常基于药物的受控给药来评估耐受性。在这项工作中,我们回顾了非甾体抗炎药超敏反应的最新知识,包括诊断方法和遗传研究。

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