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滑膜组织研究:最新综述。

Synovial tissue research: a state-of-the-art review.

机构信息

Centre for Arthritis and Rheumatic Disease, University College Dublin, Dublin Academic Medical Centre, St. Vincent's University Hospital, Elm Park, Dublin 4, Ireland.

Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Av. Prof. Egas Moniz, 1649-035, Lisbon, Portugal.

出版信息

Nat Rev Rheumatol. 2017 Aug;13(8):463-475. doi: 10.1038/nrrheum.2017.115. Epub 2017 Jul 13.

DOI:10.1038/nrrheum.2017.115
PMID:28701760
Abstract

The synovium is the major target tissue of inflammatory arthritides such as rheumatoid arthritis. The study of synovial tissue has advanced considerably throughout the past few decades from arthroplasty and blind needle biopsy to the use of arthroscopic and ultrasonographic technologies that enable easier visualization and improve the reliability of synovial biopsies. Rapid progress has been made in using synovial tissue to study disease pathogenesis, to stratify patients, to discover biomarkers and novel targets, and to validate therapies, and this progress has been facilitated by increasingly diverse and sophisticated analytical and technological approaches. In this Review, we describe these approaches, and summarize how their use in synovial tissue research has improved our understanding of rheumatoid arthritis and identified candidate biomarkers that could be used in disease diagnosis and stratification, as well as in predicting disease course and treatment response.

摘要

滑膜是类风湿关节炎等炎性关节炎的主要靶组织。在过去几十年中,滑膜组织的研究取得了长足的进展,从关节置换和盲针活检到关节镜和超声技术的应用,这些技术使滑膜活检更容易可视化,并提高了其可靠性。利用滑膜组织研究疾病发病机制、对患者进行分层、发现生物标志物和新靶点以及验证治疗方法方面也取得了快速进展,而这些进展得益于越来越多样化和复杂的分析和技术方法。在这篇综述中,我们描述了这些方法,并总结了它们在滑膜组织研究中的应用如何增进我们对类风湿关节炎的理解,并确定了一些候选生物标志物,这些标志物可用于疾病诊断和分层,以及预测疾病进程和治疗反应。

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本文引用的文献

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Epigenetically-driven anatomical diversity of synovial fibroblasts guides joint-specific fibroblast functions.表观遗传驱动的滑膜成纤维细胞解剖多样性指导关节特异性成纤维细胞功能。
Nat Commun. 2017 Mar 23;8:14852. doi: 10.1038/ncomms14852.
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Immunopathogenesis of Rheumatoid Arthritis.类风湿关节炎的免疫发病机制
Immunity. 2017 Feb 21;46(2):183-196. doi: 10.1016/j.immuni.2017.02.006.
3
Ex-Th17 (Nonclassical Th1) Cells Are Functionally Distinct from Classical Th1 and Th17 Cells and Are Not Constrained by Regulatory T Cells.前Th17(非经典Th1)细胞在功能上与经典Th1和Th17细胞不同,且不受调节性T细胞的限制。
夜间服用巴瑞替尼可使类风湿关节炎患者迅速产生药物反应:一项多中心非随机对照研究
Arthritis Res Ther. 2025 Apr 17;27(1):91. doi: 10.1186/s13075-025-03555-2.
4
Role of polyphenolics in the management of rheumatoid arthritis through intracellular signaling pathways: a mechanistic review.多酚类物质通过细胞内信号通路在类风湿关节炎管理中的作用:一项机制综述
Inflammopharmacology. 2025 Apr 12. doi: 10.1007/s10787-025-01731-z.
5
CUR-PDT induces ferroptosis of RA-FLS via the Nrf2/xCT/GPX4 pathway to inhibit proliferation in rheumatoid arthritis.姜黄素光动力疗法通过Nrf2/xCT/GPX4途径诱导类风湿关节炎成纤维样滑膜细胞铁死亡,以抑制类风湿关节炎中的细胞增殖。
Inflamm Res. 2025 Mar 14;74(1):53. doi: 10.1007/s00011-025-02019-2.
6
The Role of Thrombospondins in Osteoarthritis: from Molecular Mechanisms to Therapeutic Potential.血小板反应蛋白在骨关节炎中的作用:从分子机制到治疗潜力
Int J Biol Sci. 2025 Mar 3;21(5):2346-2359. doi: 10.7150/ijbs.103343. eCollection 2025.
7
Refining synovial inflammation assessment: A modified General Synovitis Score for active rheumatoid arthritis.优化滑膜炎症评估:一种用于活动期类风湿关节炎的改良通用滑膜炎评分
Exp Ther Med. 2025 Jan 24;29(3):58. doi: 10.3892/etm.2025.12808. eCollection 2025 Mar.
8
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Tissue Eng Part A. 2025 Feb;31(3-4):100-107. doi: 10.1089/ten.tea.2024.0221. Epub 2025 Jan 6.
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CD206+ Trem2+ macrophage accumulation in the murine knee joint after injury is associated with protection against post-traumatic osteoarthritis in MRL/MpJ mice.损伤后小鼠膝关节中CD206+ Trem2+巨噬细胞的积聚与MRL/MpJ小鼠创伤后骨关节炎的保护作用相关。
PLoS One. 2025 Jan 3;20(1):e0312587. doi: 10.1371/journal.pone.0312587. eCollection 2025.
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Medicina (Kaunas). 2024 Nov 5;60(11):1819. doi: 10.3390/medicina60111819.
J Immunol. 2017 Mar 15;198(6):2249-2259. doi: 10.4049/jimmunol.1600737. Epub 2017 Feb 6.
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Joint-specific DNA methylation and transcriptome signatures in rheumatoid arthritis identify distinct pathogenic processes.类风湿关节炎中关节特异性的 DNA 甲基化和转录组特征可识别出不同的致病过程。
Nat Commun. 2016 Jun 10;7:11849. doi: 10.1038/ncomms11849.
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How well do ACPA discriminate and predict RA in the general population: a study based on 12 590 population-representative Swedish twins.ACPA 在普通人群中鉴别和预测 RA 的效果如何:基于 12590 名具有代表性的瑞典双胞胎的研究。
Ann Rheum Dis. 2017 Jan;76(1):119-125. doi: 10.1136/annrheumdis-2015-208980. Epub 2016 Apr 28.
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Signs of immune activation and local inflammation are present in the bronchial tissue of patients with untreated early rheumatoid arthritis.在未经治疗的早期类风湿关节炎患者的支气管组织中存在免疫激活和局部炎症的迹象。
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Towards prevention of autoantibody-positive rheumatoid arthritis: from lifestyle modification to preventive treatment.迈向自身抗体阳性类风湿关节炎的预防:从生活方式改变到预防性治疗。
Rheumatology (Oxford). 2016 Apr;55(4):607-14. doi: 10.1093/rheumatology/kev347. Epub 2015 Sep 15.
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Serum RANKL levels associate with anti- citrullinated protein antibodies in early untreated rheumatoid arthritis and are modulated following methotrexate.血清RANKL水平与早期未治疗的类风湿性关节炎中的抗瓜氨酸化蛋白抗体相关,并在甲氨蝶呤治疗后受到调节。
Arthritis Res Ther. 2015 Sep 4;17(1):239. doi: 10.1186/s13075-015-0760-9.
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Acute serum amyloid A is an endogenous TLR2 ligand that mediates inflammatory and angiogenic mechanisms.急性血清淀粉样蛋白 A 是一种内源性 TLR2 配体,可介导炎症和血管生成机制。
Ann Rheum Dis. 2016 Jul;75(7):1392-8. doi: 10.1136/annrheumdis-2015-207655. Epub 2015 Aug 19.
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Key Challenges in Rheumatic and Musculoskeletal Disease Translational Research.风湿性和肌肉骨骼疾病转化研究中的关键挑战
EBioMedicine. 2014 Nov 18;1(2-3):95-6. doi: 10.1016/j.ebiom.2014.11.011. eCollection 2014 Dec.