Center for Liver Research, Institute of Biomedical Research, University of Birmingham, Birmingham B15 2TH, UK.
Toxicol Sci. 2010 Jun;115(2):307-21. doi: 10.1093/toxsci/kfq009. Epub 2010 Jan 13.
Hepatic inflammation is a common finding during a variety of liver diseases including drug-induced liver toxicity. The inflammatory phenotype can be attributed to the innate immune response generated by Kupffer cells, monocytes, neutrophils, and lymphocytes. The adaptive immune system is also influenced by the innate immune response leading to liver damage. This review summarizes recent advances in specific mechanisms of immune-mediated hepatotoxicity and its application to drug-induced liver injury. Basic mechanisms of activation of lymphocytes, macrophages, and neutrophils and their unique mechanisms of recruitment into the liver vasculature are discussed. In particular, the role of adhesion molecules and various inflammatory mediators in this process are explored. In addition, the authors describe mechanisms of liver cell damage by these inflammatory cells and critically evaluate the functional significance of each cell type for predictive and idiosyncratic drug-induced liver injury. It is expected that continued advances in our understanding of immune mechanisms of liver injury will lead to an earlier detection of the hepatotoxic potential of drugs under development and to an earlier identification of susceptible individuals at risk for predictive and idiosyncratic drug toxicities.
肝脏炎症是多种肝脏疾病的常见表现,包括药物性肝毒性。炎症表型可归因于库普弗细胞、单核细胞、中性粒细胞和淋巴细胞产生的固有免疫反应。适应性免疫系统也受到固有免疫反应的影响,导致肝损伤。这篇综述总结了免疫介导的肝毒性的特定机制的最新进展及其在药物性肝损伤中的应用。讨论了淋巴细胞、巨噬细胞和中性粒细胞的激活的基本机制及其独特的招募到肝血管系统的机制。特别是,探讨了粘附分子和各种炎症介质在这一过程中的作用。此外,作者还描述了这些炎症细胞引起的肝细胞损伤的机制,并批判性地评估了每种细胞类型对预测性和特发性药物性肝损伤的功能意义。预计我们对肝脏损伤免疫机制的理解的不断进步将导致更早地发现正在开发的药物的肝毒性潜力,并更早地发现易受预测性和特发性药物毒性影响的易感个体。