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[银屑病关节炎病理生理学中的新型分子机制]

[Novel molecular mechanisms in the pathophysiology of psoriatic arthritis].

作者信息

Simon D, Kampylafka E, Hueber A J

机构信息

Medizinische Klinik 3, Rheumatologie und Immunologie, Universitätsklinikum Erlangen, Ulmenweg 18, 91054, Erlangen, Deutschland.

出版信息

Z Rheumatol. 2018 Nov;77(9):776-782. doi: 10.1007/s00393-018-0503-9.

DOI:10.1007/s00393-018-0503-9
PMID:30003319
Abstract

The complex pathogenesis of psoriatic arthritis (PsA) is still only partially understood; however, recently a greatly improved understanding of this disease has been achieved, especially with respect to the inflammatory processes of the entheses. Thus, the clinical aspects of enthesitis increasingly differentiate PsA from other autoimmune diseases and sharpen the unique pathological clinical picture of PsA. Better pathophysiological understanding and the development of different biomarker approaches will bolster early detection of PsA. Therefore, the successful early recognition of PsA and more reliable identification of psoriasis patients at risk might be possible in the near future.

摘要

银屑病关节炎(PsA)复杂的发病机制目前仍只得到部分理解;然而,最近人们对这种疾病的认识有了很大提高,特别是在附着点炎的炎症过程方面。因此,附着点炎的临床特征越来越使PsA与其他自身免疫性疾病区分开来,并凸显出PsA独特的病理临床特征。对病理生理学的更好理解以及不同生物标志物方法的发展将有助于PsA的早期检测。因此,在不久的将来,成功早期识别PsA并更可靠地识别有风险的银屑病患者或许是可能的。

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1
[Novel molecular mechanisms in the pathophysiology of psoriatic arthritis].[银屑病关节炎病理生理学中的新型分子机制]
Z Rheumatol. 2018 Nov;77(9):776-782. doi: 10.1007/s00393-018-0503-9.
2
Enthesitis: an autoinflammatory lesion linking nail and joint involvement in psoriatic disease.附着点炎:一种将银屑病中指甲和关节受累联系起来的自身炎症性病变。
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Pathogenesis of psoriatic arthritis.银屑病关节炎的发病机制。
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Management of psoriatic arthritis: Early diagnosis, monitoring of disease severity and cutting edge therapies.银屑病关节炎的治疗:早期诊断、疾病严重程度监测和前沿治疗。
J Autoimmun. 2017 Jan;76:21-37. doi: 10.1016/j.jaut.2016.10.009. Epub 2016 Nov 9.

本文引用的文献

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A systematic review and meta-analysis of the efficacy and safety of the interleukin (IL)-12/23 and IL-17 inhibitors ustekinumab, secukinumab, ixekizumab, brodalumab, guselkumab and tildrakizumab for the treatment of moderate to severe plaque psoriasis.白细胞介素(IL)-12/23和IL-17抑制剂优特克单抗、司库奇尤单抗、依奇珠单抗、布罗达单抗、古塞库单抗和替拉珠单抗治疗中度至重度斑块状银屑病疗效和安全性的系统评价与荟萃分析
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Genetic polymorphisms associated with psoriasis and development of psoriatic arthritis in patients with psoriasis.与银屑病及银屑病患者发生银屑病关节炎相关的基因多态性。
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Exploring the Psoriatic Arthritis Proteome in Search of Novel Biomarkers.探索银屑病关节炎蛋白质组以寻找新型生物标志物。
Proteomes. 2018 Jan 24;6(1):5. doi: 10.3390/proteomes6010005.
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Early and sustained efficacy with apremilast monotherapy in biological-naïve patients with psoriatic arthritis: a phase IIIB, randomised controlled trial (ACTIVE).生物制剂初治的银屑病关节炎患者接受阿普米司特单药治疗的早期和持续疗效:一项 IIIB 期、随机对照试验(ACTIVE)。
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Altered Bone Remodeling in Psoriatic Disease: New Insights and Future Directions.银屑病中的骨重塑改变:新的见解与未来方向。
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Cutting Edge: Homeostasis of Innate Lymphoid Cells Is Imbalanced in Psoriatic Arthritis.前沿:银屑病关节炎中固有淋巴细胞的稳态失衡。
J Immunol. 2018 Feb 15;200(4):1249-1254. doi: 10.4049/jimmunol.1700596. Epub 2018 Jan 12.
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Dual IL-17A and IL-17F neutralisation by bimekizumab in psoriatic arthritis: evidence from preclinical experiments and a randomised placebo-controlled clinical trial that IL-17F contributes to human chronic tissue inflammation.双靶标 IL-17A 和 IL-17F 抑制剂布美单抗治疗银屑病关节炎:临床前实验和随机安慰剂对照临床试验的证据表明,IL-17F 参与了人类慢性组织炎症。
Ann Rheum Dis. 2018 Apr;77(4):523-532. doi: 10.1136/annrheumdis-2017-212127. Epub 2017 Dec 23.
8
Efficacy and Safety of Ixekizumab in Patients with Active Psoriatic Arthritis: 52-week Results from a Phase III Study (SPIRIT-P1).依奇珠单抗治疗活动性银屑病关节炎患者的疗效和安全性:一项 III 期研究(SPIRIT-P1)的 52 周结果。
J Rheumatol. 2018 Mar;45(3):367-377. doi: 10.3899/jrheum.170429. Epub 2017 Dec 15.
9
and are disease-specific biomarkers for psoriatic arthritis susceptibility.[具体内容]和[具体内容]是银屑病关节炎易感性的疾病特异性生物标志物。 (你提供的原文“and are”表述不完整,这里只是根据形式给出大致译文框架,你可补充完整原文后追问我准确译文 )
Oncotarget. 2017 Sep 8;8(56):95401-95411. doi: 10.18632/oncotarget.20727. eCollection 2017 Nov 10.
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Enthesitis: from pathophysiology to treatment.附着点炎:从病理生理学到治疗。
Nat Rev Rheumatol. 2017 Nov 21;13(12):731-741. doi: 10.1038/nrrheum.2017.188.