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Mechanistic Modelling of Drug-Induced Liver Injury: Investigating the Role of Innate Immune Responses

机译:药物引起的肝损伤的机制模型:调查先天免疫反应的作用。

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摘要

Drug-induced liver injury (DILI) remains an adverse event of significant concern for drug development and marketed drugs, and the field would benefit from better tools to identify liver liabilities early in development and/or to mitigate potential DILI risk in otherwise promising drugs. DILIsym software takes a quantitative systems toxicology approach to represent DILI in pre-clinical species and in humans for the mechanistic investigation of liver toxicity. In addition to multiple intrinsic mechanisms of hepatocyte toxicity (ie, oxidative stress, bile acid accumulation, mitochondrial dysfunction), DILIsym includes the interaction between hepatocytes and cells of the innate immune response in the amplification of liver injury and in liver regeneration. The representation of innate immune responses, detailed here, consolidates much of the available data on the innate immune response in DILI within a single framework and affords the opportunity to systematically investigate the contribution of the innate response to DILI.
机译:药物诱发的肝损伤(DILI)仍然是药物开发和上市药物引起重大关注的不利事件,该领域将受益于更好的工具,可以在开发早期识别肝脏疾病和/或减轻在其他有前途的药物中潜在的DILI风险。 DILIsym软件采用定量系统毒理学方法来代表临床前物种和人类中的DILI,以进行肝脏毒性的机理研究。除了肝细胞毒性的多种内在机制(即氧化应激,胆汁酸蓄积,线粒体功能障碍)外,DILIsym还包括肝细胞与先天性免疫应答细胞之间的相互作用,以扩大肝脏损伤和肝脏再生。先天免疫应答的表示(在此详细介绍)在单个框架内整合了许多关于DILI中先天免疫应答的可用数据,并提供了系统地研究先天应答对DILI贡献的机会。

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