Brockow Knut, Romano Antonino
Department of Dermatology und Allergology Biederstein, and Division Environmental Dermatology and Allergology, Helmholtz Zentrum München/TUM, Technical University Munich, Germany.
Curr Pharm Des. 2008;14(27):2778-91. doi: 10.2174/138161208786369821.
Adverse drug reactions (ADRs) are an area of concern for pharmaceutical drug development. Among these, drug hypersensitivity reactions are neither dose-dependent nor predictable, and affect only predisposed individuals. Clinical and immunological studies suggest that IgE-mediated (type I) and cell-mediated (type-IV) pathogenic mechanisms are involved in many immediate (i.e., occurring within 1 hour after the last drug administration) and non-immediate (i.e., occurring more than 1 hour after the last drug administration) hypersensitivity reactions, respectively. Skin prick, patch, and intradermal tests are the most readily available tools for the evaluation of hypersensitivity drug reactions. The diagnostic value of skin tests for many drugs still has not been fully established. Reliable skin test procedures for the diagnosis of drug hypersensitivity have been defined, and test concentrations have been validated for many drugs. Skin tests should be carried out according to the clinical features of ADRs. In immediate drug reactions, an IgE-mediated mechanism can be demonstrated by a positive skin prick and/or intradermal test after 20 minutes, whereas in non-immediate reactions, a T-cell involvement can be found by a positive patch test and/or a late-reading intradermal test. The predictive value of skin tests varies with the drug tested and is especially high with beta-lactams, muscle relaxants, insulins, platinum salts, streptokinase, and chymopapain. Further diagnostic tests are required in the assessment of drug hypersensitivity reactions. However, skin tests can provide information about the culprit drug and the mechanism involved in certain reactions. The present review addresses literature data regarding the diagnosis of drug hypersensitivity reactions by skin tests.
药物不良反应(ADR)是药物研发中令人关注的一个领域。其中,药物过敏反应既不依赖剂量,也不可预测,仅影响易感个体。临床和免疫学研究表明,IgE介导(I型)和细胞介导(IV型)致病机制分别参与了许多速发型(即末次给药后1小时内发生)和迟发型(即末次给药后1小时以上发生)过敏反应。皮肤点刺试验、斑贴试验和皮内试验是评估药物过敏反应最常用的方法。许多药物皮肤试验的诊断价值尚未完全确立。已经定义了用于诊断药物过敏的可靠皮肤试验程序,并且许多药物的试验浓度已经得到验证。应根据药物不良反应的临床特征进行皮肤试验。在速发型药物反应中,IgE介导的机制可通过20分钟后的阳性皮肤点刺试验和/或皮内试验证实,而在迟发型反应中,可通过阳性斑贴试验和/或延迟读数皮内试验发现T细胞参与。皮肤试验的预测价值因所测试的药物而异,对于β-内酰胺类、肌肉松弛剂、胰岛素、铂盐、链激酶和木瓜凝乳蛋白酶尤其高。评估药物过敏反应需要进一步的诊断试验。然而,皮肤试验可以提供有关致病药物和某些反应所涉及机制的信息。本综述阐述了有关通过皮肤试验诊断药物过敏反应的文献数据。