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

Gene regulation and systems biology Pub Date : 2017-05-30 eCollection Date: 2017-01-01 DOI:10.1177/1177625017696074
Lisl Km Shoda, Christina Battista, Scott Q Siler, David S Pisetsky, Paul B Watkins, Brett A Howell
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引用次数: 22

Abstract

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.

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药物性肝损伤的机制建模:研究先天免疫反应的作用。
药物性肝损伤(DILI)仍然是药物开发和上市药物关注的重大不良事件,该领域将受益于更好的工具,在开发早期识别肝脏损害和/或减轻其他有希望的药物的潜在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,用于肝毒性的机制研究。除了肝细胞毒性的多种内在机制(如氧化应激、胆汁酸积累、线粒体功能障碍)外,DILIsym还包括肝细胞与先天免疫反应细胞在肝损伤放大和肝再生中的相互作用。这里详细介绍的先天免疫反应的表现,在一个单一的框架内巩固了DILI中先天免疫反应的许多可用数据,并提供了系统地研究DILI先天反应的贡献的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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