Mukherjee Upasana, Reddy P Hemachandra
Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA.
Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA; Nutritional Sciences Department, College Human Sciences, Texas Tech University, Lubbock, TX, USA; Department of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, TX, USA; Department of Neurology, Texas Tech University Health Sciences Center, Lubbock, TX, USA; Department of Public Health, Graduate School of Biomedical Sciences, Texas Tech University Health Sciences Center, Lubbock, TX, USA; Department of Speech, Language, and Hearing Sciences, Texas Tech University Health Sciences Center, Lubbock, TX, USA.
Ageing Res Rev. 2025 Sep;111:102843. doi: 10.1016/j.arr.2025.102843. Epub 2025 Jul 23.
Alzheimer's disease (AD) is increasingly recognized as a condition shaped not only by central nervous system pathology but also by complex, bidirectional interactions between the gut, brain, and immune system. This review synthesizes emerging evidence on gut-brain-immune dysregulation in AD, with particular attention to how chronic stress, microbial imbalance, and neuroimmune signaling converge to influence disease risk and progression. We move beyond traditional microbiome-focused perspectives to incorporate non-microbial gut-derived mediators, including enteroendocrine hormones, bile acids, and vagal neuropeptides, which contribute to immune modulation, neurotransmission, and brain homeostasis. Importantly, we highlight that AD-related neurodegeneration can also feedback to impair gastrointestinal function and microbial composition, creating a self-reinforcing pathological loop. The review integrates recent findings on the role of host genetic polymorphisms, such as APOE4 and TREM2, in modulating gut permeability, immune tone, and microbiota profiles-emphasizing a systems biology model in which genome-microbiome interactions shape AD susceptibility. We also explore how single-cell omics technologies and multi-organ frameworks are redefining our understanding of gut-brain-immune circuits at cellular resolution. The translational section critically evaluates current and potential therapeutic strategies, including dietary, microbial, behavioral, and endocrine interventions, while addressing the challenges of applying preclinical findings to diverse human populations across the disease spectrum. By incorporating age-, stage-, and genotype-specific considerations, this review offers a comprehensive and timely synthesis of the gut-brain-stress axis in AD, positioning it as a key frontier in mechanistic research and precision therapeutic development.
阿尔茨海默病(AD)越来越被认为不仅是一种由中枢神经系统病理学塑造的疾病,还受到肠道、大脑和免疫系统之间复杂的双向相互作用的影响。本综述综合了AD中肠道-大脑-免疫失调的新证据,特别关注慢性应激、微生物失衡和神经免疫信号如何共同影响疾病风险和进展。我们超越了传统的以微生物群为重点的观点,纳入了非微生物来源的肠道介质,包括肠内分泌激素、胆汁酸和迷走神经肽,它们有助于免疫调节、神经传递和大脑稳态。重要的是,我们强调与AD相关的神经退行性变也会反馈损害胃肠功能和微生物组成,形成一个自我强化的病理循环。该综述整合了宿主基因多态性(如APOE4和TREM2)在调节肠道通透性、免疫状态和微生物群谱方面作用的最新发现,强调了一种系统生物学模型,即基因组-微生物群相互作用塑造了AD易感性。我们还探讨了单细胞组学技术和多器官框架如何在细胞分辨率上重新定义我们对肠道-大脑-免疫回路的理解。翻译部分批判性地评估了当前和潜在的治疗策略,包括饮食、微生物、行为和内分泌干预,同时解决了将临床前研究结果应用于疾病谱中不同人群所面临的挑战。通过纳入年龄、阶段和基因型特异性因素,本综述全面且及时地综合了AD中肠道-大脑-应激轴的研究,将其定位为机制研究和精准治疗开发的关键前沿领域。