摘要
特应性皮炎(AD)是由遗传、免疫和环境因素相互作用引起的慢性瘙痒性、炎症性疾病。AD具体发病病因及机制尚不完全明确,因其遗传易感性,AD的遗传和表观遗传学研究受到很多关注。遗传学研究已经确定了多个AD遗传易感基因位点及相关候选基因。例如皮肤屏障功能障碍基因、2型T辅助淋巴细胞(Th2)型免疫相关基因等。这些遗传方面的研究有利于进一步明确AD发病机制,并可能为AD的治疗提供新的方向。
Atopic dermatitis(AD)is a chronic itching and inflammatory disease caused by the interaction of genetic,immune,and environmental factors.The specific etiology and mechanism of AD are not completely defined.Due to the genetic predisposition of AD,the genetics and epigenetics studies have drawn much attention.Genetic research has identified multiple AD genetic susceptibility gene loci and related candidate genes.For example,the skin barrier dysfunction genes and Th2 immune genes were reported.These genetic studies are conducive to further clarifying the pathogenesis of AD and may provide new directions for the treatment of AD.
作者
刘欣欣
管志伟
林扬杨
李钦峰
LIU Xin-xin;GUAN Zhi-wei;LIN Yang-yang(Department of Dermatology,Tianjin Children's Hospital(Tianjin University Children's Hospital),Tianjin 300134,China)
出处
《中国实用儿科杂志》
CSCD
北大核心
2023年第9期669-674,共6页
Chinese Journal of Practical Pediatrics
基金
天津市卫生健康委员会科技项目(编号:ZC20062)。