Yang Fangping, Yang Ying, Zhu Qinyuan, Chen Sheng-An, Fu Xiaodan, Yan Sijia, Meng Chunjie, Ma Li, Sun Xinfen, Xu Jinhua, Luo Xiaoqun, Xing Qinghe
Department of Dermatology, Huashan Hospital, Fudan University, Shanghai, China.
Children's Hospital & Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
J Investig Dermatol Symp Proc. 2015 Jul;17(1):29-31. doi: 10.1038/jidsymp.2015.6.
Cutaneous adverse drug reactions (cADRs) include mild maculopapular exanthems (MPE), Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), drug reaction with eosinophilia and systemic symptoms (DRESS) and acute generalized exanthematous pustulosis (AGEP). We used HLA high-resolution genotyping and genome wide association analysis (GWAS) to identify the genetic markers for cADRs induced by common culprit drugs in Han Chinese population. To further understand the immunopathogenesis of cADRs, and with the goal of developing treatment strategies, we compared the expression of cytoxic cytokines between the patients with cADRs and normal controls. Our data suggested that the carbamazepine induced SJS/TEN, allopurinol induced CADRs, methazolamide induced SJS/TEN and SASP induced DRESS were respectively strongly associated with HLA-B15:02, HLA-B58:01, HLA-B59:01 and HLA-B13:01. In addition, increased expression of cytotoxic cytokines in sera and tissues of cADRs patients were found, compared with healthy controls. Our findings may shed light on prediction and prevention of cADRs, provide clues to pathogenesis, and guide treatment strategies of these reactions.
皮肤药物不良反应(cADRs)包括轻度斑丘疹(MPE)、史蒂文斯-约翰逊综合征(SJS)、中毒性表皮坏死松解症(TEN)、伴有嗜酸性粒细胞增多和全身症状的药物反应(DRESS)以及急性泛发性脓疱病(AGEP)。我们采用HLA高分辨率基因分型和全基因组关联分析(GWAS)来鉴定中国汉族人群中常见致病药物诱发的cADRs的遗传标记。为了进一步了解cADRs的免疫发病机制,并以制定治疗策略为目标,我们比较了cADRs患者与正常对照之间细胞毒性细胞因子的表达。我们的数据表明,卡马西平诱发的SJS/TEN、别嘌醇诱发的CADRs、甲唑酰胺诱发的SJS/TEN以及柳氮磺胺吡啶诱发的DRESS分别与HLA-B15:02、HLA-B58:01、HLA-B59:01和HLA-B13:01密切相关。此外,与健康对照相比,发现cADRs患者血清和组织中细胞毒性细胞因子的表达增加。我们的研究结果可能有助于cADRs的预测和预防,为发病机制提供线索,并指导这些反应的治疗策略。