Oct 2026· Frontiers in Immunology· 0 citations· 256 references
TL;DR
This review comprehensively summarizes the molecular mechanisms, receptor signaling pathways, metabolic regulation, and clinical translational potential of this axis, aiming to provide theoretical support for future precision medicine and innovative therapeutic strategies.
Abstract
The gut microbiota and bile acid metabolism are intricately linked, forming a pivotal axis that regulates host immune function and metabolic homeostasis. Bile acids not only facilitate lipid digestion as surfactants but also act as key signaling molecules by activating multiple receptors, which modulate immune responses, energy metabolism, and inflammatory processes. The gut microbiota enzymatically converts primary bile acids into secondary bile acids, thereby influencing the composition and function of the bile acid pool. Dysbiosis of the gut microbiota and aberrations in bile acid signaling pathways are closely associated with various diseases. Recently, therapeutic strategies targeting the gut microbiota-bile acid-immune axis have emerged, including receptor agonists/antagonists and microbiota modulators, offering novel approaches for disease prevention and treatment. This review comprehensively summarizes the molecular mechanisms, receptor signaling pathways, metabolic regulation, and clinical translational potential of this axis, aiming to provide theoretical support for future precision medicine and innovative therapeutic strategies.
The gut microbiota is pivotal in regulating host metabolic homeostasis and is closely associated with the onset, progression, prevention, and treatment of various diseases. Endocrine fibroblast growth factors (FGFs) serve as key signaling molecules through which the gut microbiota influences host metabolic health. Via...
Xiang-Xin Ye, Zhuo-Fan Lu, Wei-Ru Zhang et al.· Zhejiang da xue xue bao. Yi...· 0 citations
The immune-regulatory network of BAs, which includes both receptor-dependent pathways and receptor-independent mechanisms, is examined, and emerging therapeutic strategies aimed at restoring metabolic-immune homeostasis are assessed.
Current evidence linking microbiota-associated metabolic networks to renal immune remodeling across different kidney diseases is summarized, highlighting metabolite origin, shared target-cell responses, disease-specific and context-dependent mechanisms, and current evidence limitations.
Hong-Kun Zhang, Tao Zhang, Zheng-Chao Pan et al.· Frontiers in Microbiology· 0 citations
The integration of multi-omics technologies, artificial intelligence, and precision microbiome-based interventions is expected to accelerate the development of personalized therapeutic strategies and enhance the clinical applicability of microbial metabolite research.
Amith Kumar, Phool Chandra, Prakhar Varshney et al.· Current pharmaceutical desig...· 0 citations
ABSTRACT The gut microbiota–tryptophan (TRP) metabolism–immune axis is one of the core pathogenic mechanisms in inflammatory bowel disease (IBD). Physiologically, gut microbes convert dietary TRP into bioactive metabolites that regulate intestinal immune balance and barrier function via AHR. In IBD, this axis enters a...