Role of immune reactions in drug-induced liver injury (DILI)

被引:60
作者
Ju, Cynthia [1 ]
Reilly, Timothy [2 ]
机构
[1] Univ Colorado Denver, Skaggs Sch Pharm, Aurora, CO 80045 USA
[2] Bristol Myers Squibb Co, Dept Toxicol Drug Safety Evaluat, Princeton, NJ USA
关键词
innate immunity; adaptive immunity; animal model; acetaminophen-induced liver injury; halothane-induced liver injury; neutrophils; Kupffer cells; NK cells; NKT cells; HALOTHANE-ASSOCIATED HEPATOTOXICITY; NECROSIS-FACTOR-ALPHA; NATURAL-KILLER-CELLS; OF-THE-LITERATURE; GUINEA-PIG MODEL; CD8(+) T-CELLS; ACETAMINOPHEN HEPATOTOXICITY; KUPFFER CELLS; HEPATIC-NECROSIS; DENDRITIC CELLS;
D O I
10.3109/03602532.2011.645579
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although some drugs cause drug-induced liver injury (DILI) through direct damage to hepatocytes or intereference with bile secretion, others cause delayed, often idiosyncratic, DILI with clinical features, such as mild lymphocytic infiltrate, that are reminiscent of allergic reactions involving activation of the adaptive immune system. Even in cases of direct drug-induced hepatotoxicity, infiltration of inflammatory cells into the liver is often observed, suggesting a role for the innate immune system (e. g., neutrophils, macrophages, and so on). Therefore, a variety of hypotheses for the pathogenesis of DILI center around a pathogenic role of drug-(or drug-metabolite-) specific adaptive immune cells, as well as hepatic-injury-induced innate immune responses in the development, progression, and/or resolution of DILI.
引用
收藏
页码:107 / 115
页数:9
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