Hascoët Emilie, Blanchard Frédéric, Blin-Wakkach Claudine, Guicheux Jérôme, Lesclous Philippe, Cloitre Alexandra
Nantes Université, Oniris, Univ Angers, CHU Nantes, INSERM, Regenerative Medicine and Skeleton, RMeS, UMR 1229, F-44000, Nantes, France.
Université Côte d'Azur, CNRS, LP2M, Nice, France.
Bone Res. 2023 May 22;11(1):26. doi: 10.1038/s41413-023-00257-w.
Rheumatoid arthritis (RA) and periodontitis are chronic inflammatory diseases leading to increased bone resorption. Preventing this inflammatory bone resorption is a major health challenge. Both diseases share immunopathogenic similarities and a common inflammatory environment. The autoimmune response or periodontal infection stimulates certain immune actors, leading in both cases to chronic inflammation that perpetuates bone resorption. Moreover, RA and periodontitis have a strong epidemiological association that could be explained by periodontal microbial dysbiosis. This dysbiosis is believed to be involved in the initiation of RA via three mechanisms. (i) The dissemination of periodontal pathogens triggers systemic inflammation. (ii) Periodontal pathogens can induce the generation of citrullinated neoepitopes, leading to the generation of anti-citrullinated peptide autoantibodies. (iii) Intracellular danger-associated molecular patterns accelerate local and systemic inflammation. Therefore, periodontal dysbiosis could promote or sustain bone resorption in distant inflamed joints. Interestingly, in inflammatory conditions, the existence of osteoclasts distinct from "classical osteoclasts" has recently been reported. They have proinflammatory origins and functions. Several populations of osteoclast precursors have been described in RA, such as classical monocytes, a dendritic cell subtype, and arthritis-associated osteoclastogenic macrophages. The aim of this review is to synthesize knowledge on osteoclasts and their precursors in inflammatory conditions, especially in RA and periodontitis. Special attention will be given to recent data related to RA that could be of potential value in periodontitis due to the immunopathogenic similarities between the two diseases. Improving our understanding of these pathogenic mechanisms should lead to the identification of new therapeutic targets involved in the pathological inflammatory bone resorption associated with these diseases.
类风湿性关节炎(RA)和牙周炎是导致骨吸收增加的慢性炎症性疾病。预防这种炎症性骨吸收是一项重大的健康挑战。这两种疾病在免疫发病机制上具有相似性,且存在共同的炎症环境。自身免疫反应或牙周感染会刺激某些免疫因子,在这两种情况下都会导致慢性炎症,使骨吸收持续存在。此外,RA和牙周炎在流行病学上有很强的关联,这可能是由牙周微生物群落失调所解释的。据信这种失调通过三种机制参与RA的发病。(i)牙周病原体的传播引发全身炎症。(ii)牙周病原体可诱导瓜氨酸化新表位的产生,从而导致抗瓜氨酸化肽自身抗体的产生。(iii)细胞内危险相关分子模式加速局部和全身炎症。因此,牙周失调可能会促进或维持远处炎症关节的骨吸收。有趣的是,在炎症条件下,最近有报道称存在与“经典破骨细胞”不同的破骨细胞。它们具有促炎起源和功能。在RA中已描述了几种破骨细胞前体细胞群,如经典单核细胞、一种树突状细胞亚型以及与关节炎相关的破骨细胞生成巨噬细胞。本综述的目的是综合炎症条件下,特别是在RA和牙周炎中关于破骨细胞及其前体细胞的知识。由于这两种疾病在免疫发病机制上的相似性,将特别关注与RA相关的最新数据,这些数据可能对牙周炎具有潜在价值。增进我们对这些致病机制的理解应有助于确定与这些疾病相关的病理性炎症性骨吸收中涉及的新治疗靶点。