Current treatment and molecular targets for axial spondyloarthritis: Evidence from randomized controlled trials

IF 4 3区 医学 Q1 PHARMACOLOGY & PHARMACY Current Opinion in Pharmacology Pub Date : 2022-12-01 DOI:10.1016/j.coph.2022.102307
Rouhin Sen , Liron Caplan
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引用次数: 2

Abstract

Axial spondyloarthritis (axSpA) is a chronic inflammatory disease that predominantly affects the axial skeleton and is characterized by inflammatory back pain. While much has been published regarding non-steroidal anti-inflammatory drugs and tumor necrosis factor inhibitors, other classes of medications which leverage alternate molecular mechanisms receive less attention. In this review, we summarize a few of the novel targets in axSpA, review the putative mechanism of action of therapies that focus on these targets, and reference the germane recently completed, ongoing, or proposed randomized controlled clinical trials. The agents addressed include inhibitors of interleukin-23, interleukin-17, janus kinases, granulocyte-macrophage colony-stimulating factor, macrophage migration inhibitory factor, antibodies recognizing T cell receptor beta variable 9 gene positive clones, as well as inhibitors of mitogen-activated protein kinase-activated protein kinase-2.

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轴性脊柱炎的当前治疗和分子靶点:来自随机对照试验的证据
中轴性脊柱炎(axSpA)是一种慢性炎症性疾病,主要影响中轴骨骼,其特征是炎症性背痛。虽然关于非甾体抗炎药和肿瘤坏死因子抑制剂的研究已经发表了很多,但其他利用替代分子机制的药物却很少受到关注。在这篇综述中,我们总结了axSpA中的一些新靶点,回顾了针对这些靶点的治疗的假定作用机制,并参考了最近完成的、正在进行的或拟进行的随机对照临床试验。涉及的药物包括白细胞介素-23、白细胞介素-17、janus激酶、粒细胞-巨噬细胞集落刺激因子、巨噬细胞迁移抑制因子、识别T细胞受体β变量9基因阳性克隆的抗体,以及丝裂原活化蛋白激酶-活化蛋白激酶-2的抑制剂。
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来源期刊
CiteScore
8.80
自引率
2.50%
发文量
131
审稿时长
4-8 weeks
期刊介绍: Current Opinion in Pharmacology (COPHAR) publishes authoritative, comprehensive, and systematic reviews. COPHAR helps specialists keep up to date with a clear and readable synthesis on current advances in pharmacology and drug discovery. Expert authors annotate the most interesting papers from the expanding volume of information published today, saving valuable time and giving the reader insight on areas of importance.
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