Wang Qing, Mei Hu, Zhang Ya-Lan, Pan Xian-Chao, Tan Wen, Chao Li
College of Bioengineering, Chongqing University, Chongqing 400044, China.
Yao Xue Xue Bao. 2013 Jun;48(6):799-808.
With the advent of Twenty-First century, more and more genome-wide association studies (GWAS) showed that idiosyncratic adverse drug reactions (ADRs) were closely related with human leukocyte antigen (HLA) alleles, such as the associations of abacavir-HLA-B5701, allopurinol-HLA-B5801, and carbamazepine-HLA-B*1502, etc. To explore the mechanisms of these idiosyncratic drug reactions, hapten hypothesis, danger signal hypothesis, pharmacological interaction (P-I) concept and autoimmune mechanism are proposed. In this paper, recent GWAS studies on the HLA-mediated adverse drug reactions and underlying mechanism are reviewed in detail.
随着21世纪的到来,越来越多的全基因组关联研究(GWAS)表明,特异质性药物不良反应(ADR)与人类白细胞抗原(HLA)等位基因密切相关,如阿巴卡韦与HLA - B5701、别嘌醇与HLA - B5801以及卡马西平与HLA - B*1502等的关联。为了探究这些特异质性药物反应的机制,人们提出了半抗原假说、危险信号假说、药理相互作用(P - I)概念和自身免疫机制。本文详细综述了近期关于HLA介导的药物不良反应及其潜在机制的GWAS研究。