香港广东风湿病学会议

Mukeng Hong
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摘要

类风湿性关节炎(RA)是一种自身免疫性疾病,与肠道微生物群有关。然而,肠道微生物群是否以及如何在类风湿关节炎中发挥致病作用仍有待探索。在这里,我们观察到核酸镰刀菌富集于 RA 患者体内,并与 RA 的严重程度呈正相关。在胶原诱导的关节炎(CIA)小鼠模型中,核叉杆菌同样会加重关节炎。含有毒力决定因子 FadA 的 F. nucleatum 外膜囊泡 (OMV) 转移到关节中,引发局部炎症反应。具体来说,FadA 作用于滑膜巨噬细胞,导致参与囊泡贩运和炎症途径的 Rab5a GTPase 和炎症介质的关键调节因子 YB-1 被激活。与对照组相比,在 RA 患者中观察到了含有 FadA 的 OMV 和 Rab5a-YB-1 的高表达。这些研究结果表明,F. nucleatum 在加重 RA 病情中起着因果作用,并为临床上改善 RA 病情提供了有希望的治疗靶点。
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Hong Kong Guangdong Rheumatology Meeting
Rheumatoid arthritis (RA) is an autoimmune disorder that has been associated with the gut microbiota. However, whether and how the gut microbiota plays a pathogenic role in RA remains unexplored. Here, we observed that Fusobacterium nucleatum is enriched in RA patients and positively associated with RA severity. F. nucleatum similarly aggravates arthritis in a mouse model of collagen-induced arthritis (CIA). F. nucleatum outer membrane vesicles (OMVs) containing the virulence determinant FadA translocate into the joints, triggering local inflammatory responses. Specifically, FadA acts on synovial macrophages, resulting in the activation of the Rab5a GTPase involved in vesicle trafficking and inflammatory pathways and YB-1, a key regulator of inflammatory mediators. OMVs containing FadA and heightened Rab5a-YB-1 expression were observed in RA patients compared with controls. These findings suggest causal role of F. nucleatum in aggravating RA and provide promising therapeutic targets for clinically ameliorating RA.
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