Brodalumab: A new way to inhibit IL ‐17 in psoriasis

医学 银屑病 白细胞介素17 免疫学 塞库金单抗 发病机制 趋化因子 人口 免疫系统 银屑病性关节炎 环境卫生
作者
Paola Facheris,Mario Valenti,Giulia Pavia,Elena Guanziroli,Alessandra Narcisi,Riccardo G. Borroni,Antonio Costanzo
出处
期刊:Dermatologic Therapy [Wiley]
卷期号:33 (3) 被引量:25
标识
DOI:10.1111/dth.13403
摘要

Dermatologic TherapyVolume 33, Issue 3 e13403 Review Article Brodalumab: A new way to inhibit IL-17 in psoriasis Paola Facheris, Corresponding Author Paola Facheris paola.facheris91@gmail.com orcid.org/0000-0002-5171-9854 Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy Correspondence Paola Facheris, Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy. Email: paola.facheris91@gmail.comSearch for more papers by this authorMario Valenti, Mario Valenti Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, ItalySearch for more papers by this authorGiulia Pavia, Giulia Pavia Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, ItalySearch for more papers by this authorElena Guanziroli, Elena Guanziroli Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, ItalySearch for more papers by this authorAlessandra Narcisi, Alessandra Narcisi Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, ItalySearch for more papers by this authorRiccardo G. Borroni, Riccardo G. Borroni Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, ItalySearch for more papers by this authorAntonio Costanzo, Antonio Costanzo Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, ItalySearch for more papers by this author Paola Facheris, Corresponding Author Paola Facheris paola.facheris91@gmail.com orcid.org/0000-0002-5171-9854 Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy Correspondence Paola Facheris, Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy. Email: paola.facheris91@gmail.comSearch for more papers by this authorMario Valenti, Mario Valenti Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, ItalySearch for more papers by this authorGiulia Pavia, Giulia Pavia Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, ItalySearch for more papers by this authorElena Guanziroli, Elena Guanziroli Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, ItalySearch for more papers by this authorAlessandra Narcisi, Alessandra Narcisi Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, ItalySearch for more papers by this authorRiccardo G. Borroni, Riccardo G. Borroni Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, ItalySearch for more papers by this authorAntonio Costanzo, Antonio Costanzo Dermatology, Humanitas Clinical and Research Center - IRCCS, Rozzano, Milan, Italy Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, ItalySearch for more papers by this author First published: 13 April 2020 https://doi.org/10.1111/dth.13403Citations: 13 Paola Facheris, Mario Valenti, and Giulia Pavia should be considered joint first authors. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat 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. CONFLICT OF INTEREST The authors declare no potential conflict of interest. Citing Literature Volume33, Issue3May/June 2020e13403 RelatedInformation
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