Jin Lingyue, Xiao Jie, Luo Yuhong, Duan Lina, Gong Ying, Li Yao, Wang Haifang, Qiu Yurong, Wang Hongxia, Lai Weinan, Li Haixia
Department of Laboratory Medicine, Guangdong Provincial Key Laboratory of Precision Medical Diagnostics, Guangdong Engineering and Technology Research Center for Rapid Diagnostic Biosensors, Guangdong Provincial Key Laboratory of Single Cell Technology and Application, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, P. R. China.
Department of Internal Medicine, Division of Hematology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Clin Rev Allergy Immunol. 2025 Apr 11;68(1):42. doi: 10.1007/s12016-025-09051-4.
Systemic Lupus Erythematosus (SLE) is a complex autoimmune disease characterized by chronic inflammation and multi-organ damage, influenced by genetic, environmental, and immunological factors. Recent research highlights the significant role of gut microbiota in the pathogenesis and progression of SLE, suggesting that dysbiosis-an imbalance in the microbial community-can contribute to disease onset and severity. The gut microbiota, through its metabolites, interacts with the host's immune system, influencing immune responses and maintaining intestinal barrier integrity. These interactions have positioned the gut microbiota as a potential source of diagnostic biomarkers and therapeutic targets for SLE. This review delves into the mechanisms by which gut microbiota influences SLE, exploring how alterations in microbial composition and function can trigger autoimmune responses. We also examine the potential of gut microbiota-derived metabolites as biomarkers for early diagnosis and disease progression monitoring. Additionally, the therapeutic implications of modulating gut microbiota through dietary interventions, probiotics, prebiotics, and other microbiota-targeted therapies are discussed as promising strategies for managing SLE. The findings suggest that a deeper understanding of the gut microbiota's role in SLE could lead to more personalized and effective treatments, potentially transforming the approach to managing this chronic autoimmune condition. Future research should focus on elucidating the precise mechanisms of gut microbiota interaction with the immune system and its impact on SLE, as well as validating gut microbiota-based biomarkers and therapies in clinical settings.
系统性红斑狼疮(SLE)是一种复杂的自身免疫性疾病,其特征为慢性炎症和多器官损伤,受遗传、环境和免疫因素影响。最近的研究突出了肠道微生物群在SLE发病机制和进展中的重要作用,表明微生物群落失衡——生态失调——可能导致疾病的发生和严重程度。肠道微生物群通过其代谢产物与宿主免疫系统相互作用,影响免疫反应并维持肠道屏障完整性。这些相互作用使肠道微生物群成为SLE潜在的诊断生物标志物来源和治疗靶点。本综述深入探讨肠道微生物群影响SLE的机制,探究微生物组成和功能的改变如何引发自身免疫反应。我们还研究了肠道微生物群衍生代谢产物作为早期诊断和疾病进展监测生物标志物的潜力。此外,还讨论了通过饮食干预、益生菌、益生元及其他针对微生物群的疗法调节肠道微生物群的治疗意义,这些都是管理SLE的有前景的策略。研究结果表明,更深入地了解肠道微生物群在SLE中的作用可能会带来更个性化、更有效的治疗方法,有可能改变这种慢性自身免疫性疾病的管理方式。未来的研究应侧重于阐明肠道微生物群与免疫系统相互作用的精确机制及其对SLE的影响,以及在临床环境中验证基于肠道微生物群的生物标志物和疗法。