Literature DB >> 26666707

Ixekizumab: a new anti-IL-17A monoclonal antibody therapy for moderate-to severe plaque psoriasis.

Andrew Blauvelt1.   

Abstract

INTRODUCTION: Psoriasis is a common, systemic, inflammatory disease with prominent skin and joint manifestations. Interleukin 17A (IL-17A) has been identified as a key effector cytokine that mediates immunopathogenesis of psoriasis. Ixekizumab, a humanized monoclonal antibody that targets IL-17A, has been found in clinical trials to dramatically reduce signs and symptoms of moderate-to-severe plaque psoriasis. AREAS COVERED: The following areas are discussed: the basic structure and function of IL-17A, its role in the pathogenesis of psoriasis, the safety and efficacy of ixekizumab in clinical trials reported to date, and the possible impact of ixekizumab on the future therapeutic market for psoriasis. EXPERT OPINION: A large proportion of patients with psoriasis achieve clear or near clear skin during treatment with ixekizumab in a rapid and sustained manner. This supports the idea that IL-17A plays a central role in psoriasis immunopathogenesis. While ixekizumab has been shown to be safe in trials up to 60 weeks, long-term safety data are not yet available. Because its efficacy is higher than all previously approved drugs for psoriasis thus far, approval and use of ixekizumab may lead to a treatment paradigm change for psoriasis, where clear or near clear skin becomes an acceptable and achievable treatment goal.

Entities:  

Keywords:  Psoriasis; anti-IL17A; interleukin-17; ixekizumab

Mesh:

Substances:

Year:  2016        PMID: 26666707     DOI: 10.1517/14712598.2016.1132695

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  6 in total

1.  Updates on Psoriasis and Cutaneous Oncology: Proceedings from the 2016 MauiDerm Meeting based on presentations by.

Authors:  George Martin; Bruce E Strober; Craig L Leonardi; Joel M Gelfand; Andrew Blauvelt; Arthur Kavanaugh; Linda Stein Gold; Brian Berman; Ted Rosen; Eggert Stockfleth
Journal:  J Clin Aesthet Dermatol       Date:  2016-09-01

2.  Minimal Physiologically-Based Pharmacokinetic (mPBPK) Metamodeling of Target Engagement in Skin Informs Anti-IL17A Drug Development in Psoriasis.

Authors:  Vivaswath S Ayyar; Jong Bong Lee; Weirong Wang; Meghan Pryor; Yanli Zhuang; Thomas Wilde; An Vermeulen
Journal:  Front Pharmacol       Date:  2022-04-25       Impact factor: 5.988

3.  Tacrolimus Inhibits TNF-α/IL-17A-Produced pro-Inflammatory Effect on Human Keratinocytes by Regulating IκBζ.

Authors:  YingYing Hu; Jing Guo; Li Yin; Jie Tu; ZhiQiang Yin
Journal:  Inflammation       Date:  2020-04       Impact factor: 4.092

4.  Blocking IL-17A enhances tumor response to anti-PD-1 immunotherapy in microsatellite stable colorectal cancer.

Authors:  Chao Liu; Ruiqi Liu; Bojun Wang; Jie Lian; Yang Yao; Haoxiu Sun; Chunhui Zhang; Lin Fang; Xin Guan; Jiaqi Shi; Shuling Han; Fei Zhan; Shengnan Luo; Yuanfei Yao; Tongsen Zheng; Yanqiao Zhang
Journal:  J Immunother Cancer       Date:  2021-01       Impact factor: 13.751

5.  Mid-gestation cytokine profiles in mothers of children affected by autism spectrum disorder: a case-control study.

Authors:  Michael Carter; Sophie Casey; Gerard W O'Keeffe; Louise Gibson; Deirdre M Murray
Journal:  Sci Rep       Date:  2021-11-16       Impact factor: 4.379

6.  Pharmacokinetics, Pharmacodynamics, Safety, Tolerability, and Immunogenicity of the QX002N anti-IL-17 Monoclonal Antibody: A Phase I, Randomized, Double-Blind, Single Ascending Dose Study in Healthy Chinese Volunteers.

Authors:  Min Wu; Hong Zhang; Qianqian Li; Hong Chen; Min Fang; Lizhi Yang; Yanhua Ding
Journal:  Front Pharmacol       Date:  2022-03-04       Impact factor: 5.810

  6 in total

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