a Laboratory of Toxicology, Department of Environmental Science and Policy , Università degli Studi di Milano , Milan , Italy.
b Epidemiology and Preventive Pharmacology Centre (SEFAP), Department of Pharmacological and Biomolecular Sciences , University of Milan , Milan , Italy.
Expert Opin Drug Discov. 2018 May;13(5):425-433. doi: 10.1080/17460441.2018.1437141. Epub 2018 Feb 6.
Drug hypersensitivity reactions (DHRs) are common adverse effects of pharmaceuticals that clinically resemble allergies, and which are becoming an important burden to healthcare systems. Alongside accurate diagnostic techniques, tools which can predict potential drug-inducing hypersensitivity reactions in the pre-clinical phase are critical. Despite the important adverse reactions linked to immune-mediated hypersensitivity, at present, there are no validated or required in vivo or in vitro methods to screen the sensitizing potential of drugs and their metabolites in the pre-clinical phase. Areas covered: Enhanced prediction in preclinical safety evaluation is extremely important. The purpose of this review is to assess the state of the art of tools available to assess the allergenic potential of drugs and to highlight our current understanding of the molecular mechanisms underlying inappropriate immune activation. Expert opinion: The knowledge that allergenic drugs share common mechanisms of immune cell activation with chemical allergens, and of the definition of the mechanistic pathway to adverse outcomes, can enhance targeting toxicity testing in drug development and hazard assessment of hypersensitivity. Additional efforts and extensive resources are necessary to improve preclinical testing methodologies, including optimization, better design and interpretation of data.
药物过敏反应(DHRs)是药物的常见不良反应,临床上类似于过敏反应,并且正在成为医疗保健系统的重要负担。除了准确的诊断技术外,在临床前阶段能够预测潜在的药物诱导过敏反应的工具也至关重要。尽管与免疫介导的过敏反应相关的重要不良反应,但目前,没有经过验证或需要在临床前阶段筛选药物及其代谢物的致敏潜力的体内或体外方法。涵盖领域:在临床前安全性评估中提高预测能力非常重要。本文的目的是评估评估药物致敏潜力的工具的最新技术,并强调我们对导致免疫过度激活的分子机制的现有理解。专家意见:有知识表明,过敏药物与化学过敏原具有共同的免疫细胞激活机制,并且定义了不良后果的机制途径,这可以增强药物开发中的毒性测试靶向和过敏反应的危害评估。需要付出更多努力并投入更多资源来改进临床前测试方法,包括优化、更好地设计和解释数据。