Skip to content
Review Open access

Gut microbiota-bile acid-immune axis: receptor signaling, metabolic regulation, and therapeutic translation

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.

Read PDF

Similar papers

Review Open access Sep 2026

[Gut microbiota-mediated FGF metabolic axis in the pathogenesis, prevention and treatment of various diseases].

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. · 0 citations
Review Sep 2026

Immunomodulatory mechanisms of bile acids in autoimmune diseases along the gut-liver axis.

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.

Shuang-Ling Zhang, Xiao-Yu Xiong, Shu-Li Wei et al. · 0 citations
Review Open access Aug 2026

Microbiota-associated metabolic networks in gut-kidney communication and renal immune regulation: mechanisms and therapeutic potential

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. · 0 citations
Aug 2026

Microbial Metabolites as Systemic Signaling Molecules: Integrating Metabolism, Immunity, and Organ Crosstalk in Health and Disease.

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. · 0 citations
Review Open access Oct 2026

Evaluating traditional Chinese medicine modulation of the gut microbiota–bile acid axis in metabolic and inflammatory diseases: mechanistic evidence and translational priorities

Metabolic dysfunction-associated steatotic liver disease (MASLD), obesity, type 2 diabetes mellitus (T2D), and inflammatory bowel disease (IBD) are clinically distinct disorders that share perturbations in intestinal ecology, bile-acid composition, epithelial barrier function, and immune-metabolic regulation. Traditi...

Yan-Yan Yu, Jian Wang, Qing-Bao Yuan et al. · 0 citations
Review Open access Aug 2026

The gut microbiota-tryptophan metabolism-immune axis in inflammatory bowel disease: Mechanisms and therapeutic prospects

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...

Teng-Fei Wang, Xiao-Gan Wang, Wei-Chen Yuan · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.