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Pathogenesis and diagnosis of delayed-type drug hypersensitivity reactions, from bedside to bench and back

机译:从床旁到长凳和背部的延迟型药物超敏反应的发病机理和诊断

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摘要

Drug hypersensitivity reactions (DHR) have been present since the advent of drugs. In particular T-cell mediated delayed-type hypersensitivity reactions represent a heterogeneous clinical entity with a diverse pathogenesis and result in a considerable burden of morbidity and mortality not only driven by the reactions themselves but also by the use of alternatives which are sometimes less effective or even more dangerous. Diagnostic procedures rely on clinical history, skin testing and potential provocation testing, whereas validated in vitro diagnostic procedures are still lacking for most of them. Recent work in the field of pharmacogenomics combined with basic scientific research has provided insights in the pathogenesis of abacavir and carbamazepine hypersensitivities linked with certain human leucocyte antigen risk alleles. Nevertheless, important scientific questions on how other DHR arise and how host-drug interactions occur, remain unanswered. Recent work indicates an intricate relation between host, drug and pathogens in severe cutaneous and systemic reactions and provides more insights in the role of regulatory T-cells and viral reactivation in these reactions. In this review we focus on type IV delayed-type DHR, and address recent advances in the pathogenesis, pharmacogenomics, and diagnosis of these reactions with an emphasis on the understandings arising from basic research.
机译:自药物问世以来一直存在药物超敏反应(DHR)。特别是T细胞介导的迟发型超敏反应代表了具有不同发病机制的异质临床实体,不仅导致反应本身而且还由于使用有时效果不佳或无效的替代品,导致相当大的发病率和死亡率负担。更加危险。诊断程序依赖于临床病史,皮肤测试和潜在的激发试验,而其中大多数仍缺乏经过验证的体外诊断程序。药物基因组学领域的最新研究与基础科学研究相结合,对与某些人白细胞抗原风险等位基因相关的阿巴卡韦和卡马西平超敏反应的发病机理提供了见解。然而,关于其他DHR如何产生以及宿主药物相互作用如何发生的重要科学问题仍未得到解答。最近的工作表明,在严重的皮肤和全身反应中,宿主,药物和病原体之间存在复杂的关系,并为调节性T细胞和病毒再激活在这些反应中的作用提供了更多见解。在这篇综述中,我们着重于IV型迟发性DHR,并着重介绍了基础研究引起的理解,并探讨了这些反应的发病机制,药物基因组学和诊断方面的最新进展。

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