Pharmacogenetic Testing for Prevention of Severe Cutaneous Adverse Drug Reactions

被引:41
作者
Chang, Chih-Jung [1 ,2 ,3 ,4 ,5 ,6 ]
Chen, Chun-Bing [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ,9 ,10 ]
Hung, Shuen-Iu [1 ,2 ,3 ,4 ,7 ]
Ji, Chao [11 ]
Chung, Wen-Hung [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ,9 ,12 ,13 ]
机构
[1] Chang Gung Mem Hosp, Dept Dermatol, Taipei, Taiwan
[2] Chang Gung Mem Hosp, Drug Hypersensit Clin & Res Ctr, Taipei, Taiwan
[3] Chang Gung Mem Hosp, Dept Dermatol, Keelung, Taiwan
[4] Chang Gung Mem Hosp, Drug Hypersensit Clin & Res Ctr, Keelung, Taiwan
[5] Huaqiao Univ, Xiamen Chang Gung Hosp, Sch Med, Cent Res Lab,Dept Dermatol, Xiamen, Peoples R China
[6] Huaqiao Univ, Xiamen Chang Gung Hosp, Sch Med, Xiamen Chang Gung Allergol Consortium, Xiamen, Peoples R China
[7] Chang Gung Mem Hosp, Dept Med Res, Canc Vaccine & Immune Cell Therapy Core Lab, Taoyuan, Taiwan
[8] Chang Gung Univ, Coll Med, Taoyuan, Taiwan
[9] Chang Gung Mem Hosp, Whole Genome Res Core Lab Human Dis, Keelung, Taiwan
[10] Chang Gung Univ, Grad Inst Clin Med Sci, Taoyuan, Taiwan
[11] Fujian Med Univ, Affiliated Hosp 1, Dept Dermatol, Fuzhou, Peoples R China
[12] Tsinghua Univ, Beijing Tsinghua Chang Gung Hosp, Sch Clin Med, Dept Dermatol, Beijing, Peoples R China
[13] Shanghai Jiao Tong Univ, Sch Med, Shanghai, Peoples R China
来源
FRONTIERS IN PHARMACOLOGY | 2020年 / 11卷
关键词
drug hypersensitivity; pharmacogenetics; severe cutaneous adverse reactions; human-leukocyte antigen; T cell receptor; STEVENS-JOHNSON-SYNDROME; TOXIC EPIDERMAL NECROLYSIS; COST-EFFECTIVENESS ANALYSIS; HLA CLASS-I; INDUCED LIVER-INJURY; HLA-B-ASTERISK-1502; ALLELE; T-CELLS; HYPERSENSITIVITY REACTIONS; JAPANESE PATIENTS; ALLOPURINOL HYPERSENSITIVITY;
D O I
10.3389/fphar.2020.00969
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Severe cutaneous adverse reactions (SCAR), such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug rash with eosinophilia and systemic symptoms (DRESS), are idiosyncratic and unpredictable drug-hypersensitivity reactions with a high-mortality rate ranging from 10% to over 30%, thus causing a major burden on the healthcare system. Recent pharmacogenomic studies have revealed strong associations between SCAR and the genes encoding human-leukocyte antigens (HLAs) or drug-metabolizing enzymes. Some of pharmacogenetic markers have been successfully applied in clinical practice to protect patients from SCAR, such as HLA-B*15:02 and HLA-A*31:01 for new users of carbamazepine, HLA-B*58:01 for allopurinol, and HLA-B*57:01 for abacavir. This article aims to update the current knowledge in the field of pharmacogenomics of drug hypersensitivities or SCAR, and its implementation in the clinical practice.
引用
收藏
页数:11
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