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脊柱关节炎中白细胞介素-23/白细胞介素-17轴:从 bench 到 bedside(此处 bench 直译为实验台,结合语境可理解为基础研究,bedside 直译为床边,结合语境可理解为临床应用,整体意思是从基础研究到临床应用)

IL-23/IL-17 axis in spondyloarthritis-bench to bedside.

作者信息

Raychaudhuri Siba P, Raychaudhuri Smriti K

机构信息

Internal Medicine/Rheumatology, VA Medical Center Sacramento, Mather, CA, USA.

School of Medicine, University of California Davis, Davis, CA, USA.

出版信息

Clin Rheumatol. 2016 Jun;35(6):1437-41. doi: 10.1007/s10067-016-3263-4. Epub 2016 Apr 13.

Abstract

Cytokines play a critical role in the pathogenesis of psoriatic arthritis, ankylosing spondylitis, and other types of spondyloarthritis (SpA). Besides IFN-γ and TNF-α; IL-23/IL-17 cytokines play a dominant role in the inflammatory and proliferative cascades of SpA. Recently, in a series of elegant experiments using mouse models and human tissues, it has been demonstrated that IL-23-induced Th17 cytokines (IL-17 and IL-22) can contribute to following pathologic events associated with SpA: development of psoriatic plaque, pannus formation in the joint, joint erosion, and new bone formation. In this review article, we have discussed the contributing role of the IL-23/IL-17 cytokine axis in the pathogenesis of PsA and AS. IL-23/IL-17-targeted therapies are very promising for SpA, and we have provided an outline about usefulness of these new groups of biologics in SpA.

摘要

细胞因子在银屑病关节炎、强直性脊柱炎及其他类型的脊柱关节炎(SpA)发病机制中起关键作用。除了干扰素-γ和肿瘤坏死因子-α外,白细胞介素-23/白细胞介素-17细胞因子在脊柱关节炎的炎症和增殖级联反应中起主导作用。最近,通过一系列使用小鼠模型和人体组织的精妙实验证明,白细胞介素-23诱导的辅助性T细胞17细胞因子(白细胞介素-17和白细胞介素-22)可导致与脊柱关节炎相关的以下病理事件:银屑病斑块形成、关节血管翳形成、关节侵蚀和新骨形成。在这篇综述文章中,我们讨论了白细胞介素-23/白细胞介素-17细胞因子轴在银屑病关节炎和强直性脊柱炎发病机制中的作用。针对白细胞介素-23/白细胞介素-17的治疗方法对脊柱关节炎非常有前景,并且我们概述了这些新型生物制剂在脊柱关节炎中的效用。

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