4.7 Review

Idiosyncratic Drug-Induced Liver Injury: Mechanistic and Clinical Challenges

期刊

出版社

MDPI
DOI: 10.3390/ijms22062954

关键词

liver injury; adverse drug reactions; immunotoxicity; innate immune response; damage-associated molecular pattern molecules; reactive metabolites; cytochromes P450

资金

  1. Canadian Institutes of Health Research [142329]
  2. Natural Sciences and Engineering Research Council of Canada
  3. Ontario Graduate Scholarship
  4. MITACs research training award
  5. University of Toronto Fellowship

向作者/读者索取更多资源

IDILI remains a significant problem for patients and drug development due to its idiosyncratic nature. Most cases of IDILI are likely caused by reactive metabolites of drugs and mediated by the adaptive immune system, with some associations with specific human leukocyte antigen haplotypes.
Idiosyncratic drug-induced liver injury (IDILI) remains a significant problem for patients and drug development. The idiosyncratic nature of IDILI makes mechanistic studies difficult, and little is known of its pathogenesis for certain. Circumstantial evidence suggests that most, but not all, IDILI is caused by reactive metabolites of drugs that are bioactivated by cytochromes P450 and other enzymes in the liver. Additionally, there is overwhelming evidence that most IDILI is mediated by the adaptive immune system; one example being the association of IDILI caused by specific drugs with specific human leukocyte antigen (HLA) haplotypes, and this may in part explain the idiosyncratic nature of these reactions. The T cell receptor repertoire likely also contributes to the idiosyncratic nature. Although most of the liver injury is likely mediated by the adaptive immune system, specifically cytotoxic CD8+ T cells, adaptive immune activation first requires an innate immune response to activate antigen presenting cells and produce cytokines required for T cell proliferation. This innate response is likely caused by either a reactive metabolite or some form of cell stress that is clinically silent but not idiosyncratic. If this is true it would make it possible to study the early steps in the immune response that in some patients can lead to IDILI. Other hypotheses have been proposed, such as mitochondrial injury, inhibition of the bile salt export pump, unfolded protein response, and oxidative stress although, in most cases, it is likely that they are also involved in the initiation of an immune response rather than representing a completely separate mechanism. Using the clinical manifestations of liver injury from a number of examples of IDILI-associated drugs, this review aims to summarize and illustrate these mechanistic hypotheses.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据