Detection of HLA-B☆58:01, the susceptible allele for allopurinol-induced hypersensitivity, by loop-mediated isothermal amplification

被引:10
作者
Kwok, J. [1 ]
Kwong, K. M. [1 ]
机构
[1] Queen Mary Hosp, Div Transplantat & Immunogenet, Dept Pathol & Clin Biochem, Hong Kong, Hong Kong, Peoples R China
关键词
TOXIC EPIDERMAL NECROLYSIS; STEVENS-JOHNSON-SYNDROME; PHARMACOGENETICS;
D O I
10.1111/bjd.12097
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Allopurinol, a common medication for gout treatment, can cause rare but life-threatening severe cutaneous adverse reactions. A strong pharmacogenetic association of human leucocyte antigen (HLA)-B*58:01 with allopurinol-induced drug hypersensitivity has been reported, especially in the Han Chinese population. Objectives To develop a rapid and simple loop-mediated isothermal amplification (LAMP) assay of HLA-B*58:01 and evaluate its feasibility in predicting allopurinol-induced drug hypersensitivity. Methods Two sets of LAMP primers targeting exons 2 and 3 of HLA-B*58: 01 were designed. DNA extracted from 20 clinical blood samples of patients with gout was used to evaluate the effectiveness of the two LAMP primer sets for the detection of HLA-B*58:01. Results The results were compared with routine clinical genotyping methods. All extracted DNA samples tested with the HLA-B*58:01 LAMP assay showed agreement with the routine genotyping results. No amplifications were observed when unextracted blood samples were tested. Conclusions The HLA-B*58:01 LAMP assay was confirmed to be simple, rapid and specific for the detection of HLA-B*58:01, and therefore of potential value in the diagnosis of allopurinol-induced hypersensitivity.
引用
收藏
页码:526 / 532
页数:7
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