Galbiati Valentina, Papale Angela, Kummer Elena, Corsini Emanuela
Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano Milan, Italy.
Front Pharmacol. 2016 Jul 12;7:204. doi: 10.3389/fphar.2016.00204. eCollection 2016.
Hypersensitivity drug reactions (HDRs) are the adverse effect of pharmaceuticals that clinically resemble allergy. HDRs account for approximately 1/6 of drug-induced adverse effects, and include immune-mediated ("allergic") and non-immune-mediated ("pseudo allergic") reactions. In recent years, the severe and unpredicted drug adverse events clearly indicate that the immune system can be a critical target of drugs. Enhanced prediction in preclinical safety evaluation is, therefore, crucial. Nowadays, there are no validated in vitro or in vivo methods to screen the sensitizing potential of drugs in the pre-clinical phase. The problem of non-predictability of immunologically-based hypersensitivity reactions is related to the lack of appropriate experimental models rather than to the lack of -understanding of the adverse phenomenon. We recently established experimental conditions and markers to correctly identify drug associated with in vivo hypersensitivity reactions using THP-1 cells and IL-8 production, CD86 and CD54 expression. The proposed in vitro method benefits from a rationalistic approach with the idea that allergenic drugs share with chemical allergens common mechanisms of cell activation. This assay can be easily incorporated into drug development for hazard identification of drugs, which may have the potential to cause in vivo hypersensitivity reactions. The purpose of this review is to assess the state of the art of in vitro models to assess the allergenic potential of drugs based on the activation of dendritic cells.
药物超敏反应(HDRs)是临床上类似于过敏反应的药物不良反应。HDRs约占药物引起的不良反应的1/6,包括免疫介导(“过敏”)和非免疫介导(“假过敏”)反应。近年来,严重且不可预测的药物不良事件清楚地表明,免疫系统可能是药物的关键靶点。因此,在临床前安全性评估中加强预测至关重要。目前,尚无经过验证的体外或体内方法来在临床前阶段筛选药物的致敏潜力。基于免疫的超敏反应不可预测的问题与缺乏合适的实验模型有关,而非对不良现象缺乏了解。我们最近建立了实验条件和标志物,以利用THP-1细胞以及白细胞介素-8的产生、CD86和CD54的表达来正确识别与体内超敏反应相关的药物。所提出的体外方法得益于一种理性方法,其理念是致敏药物与化学过敏原具有共同的细胞激活机制。该检测方法可轻松纳入药物研发过程,用于识别可能具有引起体内超敏反应潜力的药物的危险性。本综述的目的是评估基于树突状细胞激活来评估药物致敏潜力的体外模型的现状。