Kuhn Kristine A, Yomogida Kentaro, Knoop Kathryn, Wu Hsin-Jung Joyce, Zaiss Mario M
Division of Rheumatology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Department of Paediatrics, Rheumatology Section, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Nat Rev Rheumatol. 2025 Jul 31. doi: 10.1038/s41584-025-01282-1.
The gut microbiome forms an ecosystem that provides the host with numerous benefits such as digestion with nutrient generation, protection from pathogens and immune system maturation. Alterations in the microbial ecosystem associated with rheumatoid arthritis and spondyloarthritis have led to the gut-joint hypothesis, which postulates that these ecological changes cause immune dysfunction that contributes to the development of arthritis. Mechanisms by which dysbiosis might trigger arthritis include molecular mimicry, dysregulation of mucosal immunity, microbial translocation, production of immunomodulatory metabolites and immune cell trafficking. We discuss the data supporting each of these mechanisms, and highlight misconceptions, limitations and gaps in knowledge. In particular, we advise against the term 'leaky-gut' as the mechanisms and effects on the immune system of intestinal permeability and bacterial translocation are distinct. Nevertheless, rheumatoid arthritis and spondyloarthritis possibly result from the convergence of multiple pathways that could be unique to subgroups of individuals within these diseases. To move the field forward, each mechanism needs to be considered through the use of model organisms and interventional trials, individually and in concert.
肠道微生物群形成了一个生态系统,为宿主提供了许多益处,如消化并产生营养物质、抵御病原体以及促进免疫系统成熟。与类风湿性关节炎和脊柱关节炎相关的微生物生态系统改变引发了肠-关节假说,该假说假定这些生态变化会导致免疫功能紊乱,进而促使关节炎的发展。生态失调可能引发关节炎的机制包括分子模拟、黏膜免疫失调、微生物易位、免疫调节代谢产物的产生以及免疫细胞迁移。我们讨论了支持上述每种机制的数据,并强调了误解、局限性和知识空白。特别是,我们不建议使用“肠漏”一词,因为肠道通透性和细菌易位对免疫系统的机制和影响是不同的。然而,类风湿性关节炎和脊柱关节炎可能是由多种途径共同作用导致的,这些途径可能在这些疾病患者的亚组中具有独特性。为推动该领域的发展,需要通过使用模式生物和干预试验,单独或协同地对每种机制进行研究。