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布罗达单抗:治疗银屑病中抑制白细胞介素-17的新方法。

Brodalumab: A new way to inhibit IL-17 in psoriasis.

作者信息

Facheris Paola, Valenti Mario, Pavia Giulia, Guanziroli Elena, Narcisi Alessandra, Borroni Riccardo G, Costanzo Antonio

机构信息

Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy.

Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.

出版信息

Dermatol Ther. 2020 May;33(3):e13403. doi: 10.1111/dth.13403. Epub 2020 Apr 27.

DOI:10.1111/dth.13403
PMID:32285564
Abstract

Psoriasis is a chronic inflammatory disease that affects 2% to 4% of the population; about 20% of the patients present a moderate-to-severe form. The IL-23/Th17/IL-17 molecular axis is considered crucial in the pathogenesis of psoriasis and IL-17 is fundamental in the maintenance of the immune and inflammatory alterations causing psoriasis. Expression of IL-17A, IL-17F, and IL-17C is strongly increased in psoriatic plaques. Effective therapy leads to restoration of the expression of a wide range of genes (including effector cytokines and chemokines downstream of IL-17) to near normal levels. Brodalumab is the first biologic drug targeting specifically the subunit A of the IL-17 receptor (IL-17RA) and thus inhibiting not only IL-17A but also other members of the IL-17 family. Brodalumab is very effective and safe in treating moderate-to severe psoriasis.

摘要

银屑病是一种慢性炎症性疾病,影响2%至4%的人口;约20%的患者呈现中重度形式。IL-23/Th17/IL-17分子轴被认为在银屑病发病机制中至关重要,而IL-17在维持导致银屑病的免疫和炎症改变中起关键作用。IL-17A、IL-17F和IL-17C在银屑病斑块中的表达显著增加。有效的治疗可使多种基因(包括IL-17下游的效应细胞因子和趋化因子)的表达恢复到接近正常水平。布罗达单抗是首个特异性靶向IL-17受体(IL-17RA)亚基A的生物药物,因此不仅抑制IL-17A,还抑制IL-17家族的其他成员。布罗达单抗在治疗中重度银屑病方面非常有效且安全。

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