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In vitro Models to Evaluate Drug-Induced Hypersensitivity: Potential Test Based on Activation of Dendritic Cells

机译:评价药物引起的超敏反应的体外模型:基于树突状细胞激活的潜在测试

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摘要

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.
机译:过敏反应(HDR)是临床上类似于变态反应的药物的不良反应。 HDR约占药物引起的不良反应的1/6,包括免疫介导的(“过敏”)反应和非免疫介导的(“伪过敏”)反应。近年来,严重且无法预测的药物不良事件清楚地表明免疫系统可以成为药物的重要靶标。因此,在临床前安全性评估中增强预测至关重要。如今,尚无经过验证的体外或体内方法来筛选临床前阶段药物的致敏潜力。基于免疫学的超敏反应的不可预测性问题与缺乏合适的实验模型有关,而不是与对不良现象的缺乏了解有关。我们最近建立了实验条件和标记,以正确鉴定与使用THP-1细胞和IL-8产生,CD86和CD54表达的体内超敏反应相关的药物。所提出的体外方法得益于一种合理的方法,其思想是致敏药物与化学致敏原共有共同的细胞激活机制。这种测定法可以很容易地并入药物开发中以进行药物的危险性鉴定,这可能会引起体内超敏反应。这篇综述的目的是评估体外模型的技术水平,以基于树突状细胞的活化来评估药物的致敏潜力。

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