Wu Dehong, Yin Mengdi, Cao Dandan, Zhang Xiafeng, Zhu Yichun, Wei Ying, Li Yiling, Wen Chengping, Zhou Jia
Department of Rheumatology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang, 310005, People's Republic of China.
Institute of Basic Research in Clinical Medicine, College of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, People's Republic of China.
J Inflamm Res. 2025 Feb 4;18:1703-1717. doi: 10.2147/JIR.S502980. eCollection 2025.
Rheumatoid arthritis (RA) is a chronic autoimmune disease and increasing evidence suggests that disturbances in the composition and function of gut microbiota are potentially implicated in the progression of RA. Further revealing the microbiota and related metabolic disorders in the preclinical stage of RA (pre-RA) is of great significance for exploration of disease mechanisms.
DBA/1 mice were injected with type II collagen on days 0 and 21 to establish collagen-induced arthritis (CIA) mouse model. Footpad thickness, serum autoantibodies, and joint histopathology were used to assess the progression of RA. A combination of 16S rRNA sequencing, untargeted metabolomics and targeted short-chain fatty acids (SCFAs) analysis were employed to comprehensively investigate the alterations of gut microbiota and fecal metabolites in CIA during the pre-RA stage.
20 days after the initial collagen immunization, CIA mice showed immune responses without joint symptoms, alongside gut microbiota disruption. Alterations were observed in 20 microbial taxa, including , etc. Untargeted and targeted metabolomics identified 33 altered fecal metabolites, mainly including sugars and their derivatives, amino acids, long-chain fatty acids and SCFAs, etc. Correlation analysis showed significant correlations between specific gut microbial abundances and fecal metabolite levels. Especially, SCFAs were strongly associated with , and .
These findings suggest that collagen immunization leads to disruption of gut microbiome and induces changes of fecal metabolites in mice, which may play a key role in early development of RA in CIA mice.
类风湿关节炎(RA)是一种慢性自身免疫性疾病,越来越多的证据表明肠道微生物群的组成和功能紊乱可能与RA的进展有关。进一步揭示RA临床前期(pre-RA)的微生物群及其相关代谢紊乱对于探索疾病机制具有重要意义。
在第0天和第21天给DBA/1小鼠注射II型胶原以建立胶原诱导的关节炎(CIA)小鼠模型。通过足垫厚度、血清自身抗体和关节组织病理学来评估RA的进展。采用16S rRNA测序、非靶向代谢组学和靶向短链脂肪酸(SCFA)分析相结合的方法,全面研究CIA小鼠在pre-RA阶段肠道微生物群和粪便代谢物的变化。
初次胶原免疫后20天,CIA小鼠出现免疫反应但无关节症状,同时肠道微生物群受到破坏。观察到20种微生物分类群发生变化,包括等。非靶向和靶向代谢组学鉴定出33种粪便代谢物发生改变,主要包括糖类及其衍生物、氨基酸、长链脂肪酸和SCFA等。相关性分析表明特定肠道微生物丰度与粪便代谢物水平之间存在显著相关性。特别是,SCFA与、和密切相关。
这些发现表明胶原免疫导致小鼠肠道微生物群破坏并诱导粪便代谢物变化,这可能在CIA小鼠RA的早期发展中起关键作用。