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[特异质药物不良反应与人类白细胞抗原等位基因的关联及其潜在机制]

[The associations between idiosyncratic adverse drug reactions and HLA alleles and their underlying mechanism].

作者信息

Wang Qing, Mei Hu, Zhang Ya-Lan, Pan Xian-Chao, Tan Wen, Chao Li

机构信息

College of Bioengineering, Chongqing University, Chongqing 400044, China.

出版信息

Yao Xue Xue Bao. 2013 Jun;48(6):799-808.

Abstract

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.

摘要

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。

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