Vineesh Allenki, Shah Shivani, Shah Kinjal, Zaigham Hassan Muhammad, Sapkota Ashbin, Khadka Subodh Raj, Rizwanullah Fnu, Dare Ibrahim Abdulgafar, Kanduri Hanumantharayudu Sneha, Kumar Makam Surendraiah Pavan, Ahmed Bubli, Gyullu Niftalieva
Community Medicine, Mallareddy Institute of Medical Sciences, Hyderabad, IND.
Medicine, Caribbean Medical University School of Medicine, Willemstad, CUW.
Cureus. 2025 Aug 3;17(8):e89300. doi: 10.7759/cureus.89300. eCollection 2025 Aug.
Autoimmune diseases (AIDs) are multifaceted, chronic illnesses characterized by immune dysregulation and systemic inflammation. Newer evidence has pointed a finger at the human gut microbiota, a trillion-fold population of microorganisms that inhabits the human GI tract, as a major influential modulator of immune reactivity and a significant contributor to autoimmune pathogenesis. This systematic review will seek to address how the literature correlates with systematic changes in the gut microbiota in AIDs as well as explore mechanistic associations with biological processes like intestinal permeability and modulation of the immune system, coupled with determining the effectiveness of microbiota-directed interventions. An extensive literature search was conducted in PubMed, Embase, Cochrane Central, and Web of Science, involving the availability of studies until May 2025. The eligible studies included observational studies, randomized controlled trials, and relevant mechanistic research regarding autoimmune diseases and alterations of the gut microbiome or administered interventions. Data extraction and risk of bias (ROB) assessments were performed by two independent reviewers, and a narrative synthesis with an illustrative meta-analysis was applied. Inclusion criteria were met by 10 studies, encompassing various autoimmune diseases, including systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), multiple sclerosis (MS), type 1 diabetes mellitus (T1DM), autoimmune thyroid diseases (AITDs), and psoriasis. Familiar patterns of microbiome dysbiosis were identified, such as a reduction in microbial diversity, increased intestinal permeability, and the expansion of pro-inflammatory species like . Dietary interventions, fecal microbiota transplantation, and probiotics demonstrated positive effects on clinical outcomes and immune measures across multiple studies. The meta-analysis revealed that microbiota-directed interventions significantly improved disease activity and immune response markers in AIDs, indicating a robust link between gut microbiota composition and autoimmune pathology. In autoimmune disorders, gut microbiota is a key factor in immunopathology. Gut biology as an adjunct interventional strategy provides potential in managing these diseases. Additional studies are required to help standardize methods and identify microbial targets specific to diseases that can then be addressed through therapeutic interventions.
自身免疫性疾病(AIDs)是多方面的慢性疾病,其特征为免疫失调和全身性炎症。最新证据表明,人类肠道微生物群(栖息于人类胃肠道中的数万亿微生物群体)是免疫反应的主要影响调节因子,也是自身免疫发病机制的重要促成因素。本系统综述旨在探讨文献中AIDs患者肠道微生物群的系统性变化,以及与肠道通透性和免疫系统调节等生物学过程的机制关联,同时确定微生物群导向干预措施的有效性。我们在PubMed、Embase、Cochrane Central和Web of Science上进行了广泛的文献检索,纳入截至2025年5月的研究。符合条件的研究包括观察性研究、随机对照试验以及关于自身免疫性疾病与肠道微生物组改变或所实施干预措施的相关机制研究。由两名独立评审员进行数据提取和偏倚风险(ROB)评估,并采用叙述性综合分析及说明性荟萃分析。10项研究符合纳入标准,涵盖多种自身免疫性疾病,包括系统性红斑狼疮(SLE)、类风湿关节炎(RA)、多发性硬化症(MS)、1型糖尿病(T1DM)、自身免疫性甲状腺疾病(AITDs)和银屑病。识别出了微生物群失调的常见模式,如微生物多样性降低、肠道通透性增加以及促炎物种的扩张等。多项研究表明,饮食干预、粪便微生物群移植和益生菌对临床结局和免疫指标具有积极影响。荟萃分析显示,微生物群导向干预措施显著改善了AIDs患者的疾病活动度和免疫反应标志物,表明肠道微生物群组成与自身免疫病理之间存在紧密联系。在自身免疫性疾病中,肠道微生物群是免疫病理学的关键因素。肠道生物学作为一种辅助干预策略,在管理这些疾病方面具有潜力。需要进一步研究以帮助规范方法,并确定特定疾病的微生物靶点,进而通过治疗干预加以解决。