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Dupilumab improves clinical symptoms in children with Netherton syndrome by suppressing Th2-mediated inflammation
BACKGROUND: Netherton syndrome is a rare, life-threatening autosomal recessive genetic disorder with no effective treatment yet. Skin barrier dysfunction caused by SPINK5 gene mutations is a hallmark of the disease. Antigen penetration through the defective skin and nonspecific inflammation provide...
Autores principales: | Yan, Shi, Wu, Xuege, Jiang, Jinqiu, Yu, Shijuan, Fang, Xiao, Yang, Huan, Bai, Xiaoming, Wang, Hua, Luo, Xiaoyan |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9773867/ https://www.ncbi.nlm.nih.gov/pubmed/36569942 http://dx.doi.org/10.3389/fimmu.2022.1054422 |
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