Idiosyncratic drug reactions: Current understanding

被引:203
作者
Uetrecht, Jack [1 ]
机构
[1] Univ Toronto, Leslie Dan Fac Pharm, Toronto, ON M5S 2S2, Canada
关键词
adverse drug reactions; tolerance; reactive metabolites; genetic polymorphism; biomarkers;
D O I
10.1146/annurev.pharmtox.47.120505.105150
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Clinical characteristics and circumstantial evidence suggest that idiosyncratic drug reactions are caused by reactive metabolites and are immune-mediated; however, there are few definitive data and there are likely exceptions. There are three principal hypotheses for how reactive metabolites might induce an immune-mediated idiosyncratic reaction: the hapten hypothesis, the danger hypothesis, and the PI hypothesis. It has been proposed that some idiosyncratic reactions, especially those involving the liver, represent metabolic idiosyncrasy; however, there are even less data to support this hypothesis. The unpredictable nature of these reactions makes mechanistic studies difficult. There is a very strong association with specific human leukocyte antigen (HLA) genes for certain reactions but this, has only been demonstrated for very few drugs. Animal models re p resent a very powerful tool for mechanistic studies, but the number of valid models is also limited. There may be, biomarkers of risk; however, much more work needs to be done.
引用
收藏
页码:513 / 539
页数:27
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