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Nat Immunol. 2017 May 18;18(6):612-621. doi: 10.1038/ni.3742.
2
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Eur J Immunol. 2017 Apr;47(4):607-614. doi: 10.1002/eji.201646723.
3
Effect of secukinumab on clinical and radiographic outcomes in ankylosing spondylitis: 2-year results from the randomised phase III MEASURE 1 study.司库奇尤单抗治疗强直性脊柱炎的临床和放射学疗效:随机 III 期 MEASURE 1 研究的 2 年结果。
Ann Rheum Dis. 2017 Jun;76(6):1070-1077. doi: 10.1136/annrheumdis-2016-209730. Epub 2016 Dec 13.
4
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Rheumatology (Oxford). 2017 Mar 1;56(3):488-493. doi: 10.1093/rheumatology/kew384.
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Secukinumab is superior to ustekinumab in clearing skin of subjects with moderate-to-severe plaque psoriasis up to 1 year: Results from the CLEAR study.司库奇尤单抗在清除中重度斑块型银屑病患者皮肤方面优于乌司奴单抗:来自 CLEAR 研究的结果。
J Am Acad Dermatol. 2017 Jan;76(1):60-69.e9. doi: 10.1016/j.jaad.2016.08.008. Epub 2016 Sep 20.
6
Secukinumab efficacy in anti-TNF-naive and anti-TNF-experienced subjects with active ankylosing spondylitis: results from the MEASURE 2 Study.司库奇尤单抗治疗抗 TNF 初治和抗 TNF 经治的活动性强直性脊柱炎患者的疗效:MEASURE 2 研究结果。
Ann Rheum Dis. 2017 Mar;76(3):571-592. doi: 10.1136/annrheumdis-2016-210023. Epub 2016 Aug 31.
7
Ixekizumab, an interleukin-17A specific monoclonal antibody, for the treatment of biologic-naive patients with active psoriatic arthritis: results from the 24-week randomised, double-blind, placebo-controlled and active (adalimumab)-controlled period of the phase III trial SPIRIT-P1.司库奇尤单抗,一种白细胞介素-17A特异性单克隆抗体,用于治疗初治的活动性银屑病关节炎患者:III期试验SPIRIT-P1的24周随机、双盲、安慰剂对照及活性(阿达木单抗)对照阶段的结果
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8
A Single Nucleotide Polymorphism in the Il17ra Promoter Is Associated with Functional Severity of Ankylosing Spondylitis.白细胞介素17受体A(Il17ra)启动子中的单核苷酸多态性与强直性脊柱炎的功能严重程度相关。
PLoS One. 2016 Jul 14;11(7):e0158905. doi: 10.1371/journal.pone.0158905. eCollection 2016.
9
Phase 3 Trials of Ixekizumab in Moderate-to-Severe Plaque Psoriasis.依奇珠单抗治疗中重度斑块状银屑病的 3 期临床试验。
N Engl J Med. 2016 Jul 28;375(4):345-56. doi: 10.1056/NEJMoa1512711. Epub 2016 Jun 8.
10
A prospective phase III, randomized, double-blind, placebo-controlled study of brodalumab in patients with moderate-to-severe plaque psoriasis.一项评估布罗利尤单抗治疗中重度斑块状银屑病的前瞻性 III 期、随机、双盲、安慰剂对照研究。
Br J Dermatol. 2016 Aug;175(2):273-86. doi: 10.1111/bjd.14493. Epub 2016 Jun 23.

白细胞介素-(IL-)17 在脊柱关节炎发病机制和靶向治疗中的作用。

Role of Interleukin- (IL-) 17 in the Pathogenesis and Targeted Therapies in Spondyloarthropathies.

机构信息

Department of Internal Medicine, Cathay General Hospital, Taipei, Taiwan.

Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.

出版信息

Mediators Inflamm. 2018 Feb 12;2018:2403935. doi: 10.1155/2018/2403935. eCollection 2018.

DOI:10.1155/2018/2403935
PMID:29670461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5833467/
Abstract

Spondyloarthropathy (SpA) is a unique type of joint inflammation characterized by coexisting erosive bone damage and pathological new bone formation. Previous genetic association studies have demonstrated that several cytokine pathways play a critical role in the pathogenesis of ankylosing spondylitis (AS), psoriatic arthritis (PsA), and other types of SpA. In addition to several well-known proinflammatory cytokines, recent studies suggest that IL-17 plays a pivotal role in the pathogenesis of SpA. Further evidence from human and animal studies have defined that IL-17 and IL-17-producing cells contribute to tissue inflammation, autoimmunity, and host defense, leading to the following pathologic events associated with SpA. Recently, several clinical trials targeting IL-17 pathways demonstrated the positive response of IL-17 blockade in treating AS, indicating a great potential of IL-17-targeting therapy in SpA. In this review article, we have discussed the contributing role of IL-17 and different IL-17-producing cells in the pathogenesis of SpA and provided an outline of therapeutic application of the IL-17 blockade in the treatment of SpA. Other targeted cytokines associated with IL-17 axis in SpA will also be included.

摘要

脊柱关节炎(SpA)是一种独特类型的关节炎症,其特征为同时存在侵蚀性骨损伤和病理性新骨形成。既往的遗传关联研究表明,几种细胞因子途径在强直性脊柱炎(AS)、银屑病关节炎(PsA)和其他类型的 SpA 的发病机制中起关键作用。除了几种众所周知的促炎细胞因子外,最近的研究表明,IL-17 在 SpA 的发病机制中发挥着重要作用。来自人类和动物研究的进一步证据表明,IL-17 和产生 IL-17 的细胞有助于组织炎症、自身免疫和宿主防御,导致与 SpA 相关的以下病理事件。最近,几项针对 IL-17 途径的临床试验表明,IL-17 阻断在治疗 AS 中的积极反应,表明 IL-17 靶向治疗在 SpA 中有很大的潜力。在这篇综述文章中,我们讨论了 IL-17 和不同的产生 IL-17 的细胞在 SpA 发病机制中的作用,并概述了 IL-17 阻断在治疗 SpA 中的治疗应用。还将包括与 SpA 中 IL-17 轴相关的其他靶向细胞因子。