Department of Internal Medicine 3, Rheumatology and Immunology, Friedrich Alexander University Erlangen-Nuremberg and Universitätsklinikum Erlangen, Ulmenweg 18, 91054 Erlangen, Germany.
Laboratory for Tissue Homeostasis and Disease, Skeletal Biology and Engineering Research Center, Department of Development and Regeneration, Catholic University Leuven, Herestraat 49, B-3000 Leuven, Belgium.
Nat Rev Rheumatol. 2017 Nov 21;13(12):731-741. doi: 10.1038/nrrheum.2017.188.
Entheses are the insertion sites of tendons and ligaments to the bone surface and are essential structures for locomotion. Inflammation of the entheses (enthesitis) is a key feature of psoriatic arthritis and spondyloarthritis. To date, our conceptual understanding of enthesitis remains limited. This Review provides an insight into the pathophysiology of enthesitis, addressing the role of biomechanics, prostaglandin E2-mediated vasodilation and the activation of innate immune cells in the initiation phase of enthesitis, as well as the role of entheseal IL-23-responsive cells that augment inflammation by producing pro-inflammatory mediators such as IL-17A, IL-22 and TNF. In addition, the molecular steps that translate inflammation into resident tissue responses, resulting in new bone formation, are discussed. The second part of the article summarizes the clinical features of enthesitis, and the role of clinical and imaging instruments in detecting enthesitis are discussed together with their challenges and limitations. Finally, the Review summarizes the current treatment possibilities for enthesitis based on the aforementioned pathophysiological concepts, focusing on the role of cytokine-blocking agents.
附着点是肌腱和韧带在骨表面的插入部位,是运动的重要结构。附着点炎(enthesitis)是银屑病关节炎和脊柱关节炎的一个关键特征。迄今为止,我们对附着点炎的概念理解仍然有限。这篇综述深入探讨了附着点炎的病理生理学,涉及生物力学、前列腺素 E2 介导的血管扩张以及固有免疫细胞在附着点炎起始阶段的激活作用,以及通过产生促炎介质如 IL-17A、IL-22 和 TNF 来增强炎症的附着 IL-23 反应性细胞的作用。此外,还讨论了将炎症转化为驻留组织反应从而导致新骨形成的分子步骤。文章的第二部分总结了附着点炎的临床特征,并讨论了临床和影像学仪器在检测附着点炎中的作用,以及它们的挑战和局限性。最后,综述根据上述病理生理学概念总结了附着点炎的当前治疗可能性,重点介绍了细胞因子阻断剂的作用。