Target intelligence / Profile preview

Gut microbiota–systemic inflammation pathway (null)

Target
null
Molecular classification
Other (not a receptor, enzyme, transporter, etc.; instead an integrated host–microbe signaling network)
01

Overview

The gut microbiota–systemic inflammation pathway describes a web of interactions between intestinal microbes (bacteria, fungi, archaea, and their metabolic products) and the host immune system that determines the balance between immune tolerance and inflammation. Key metabolites (such as short-chain fatty acids and tryptophan catabolites) signal through host G-protein-coupled receptors, nuclear receptors, and pattern recognition receptors (e.g., TLRs) to modulate immune responses locally in the gut and systemically. Dysbiosis, or an imbalance of gut microbes, leads to increased pro-inflammatory species, reduced anti-inflammatory microbes, and altered metabolite production, which are implicated in a wide array of inflammatory, autoimmune, and metabolic diseases. Unlike classical drug targets, this pathway represents an integrated multi-component network, not a single protein or receptor

Other names
gut microbiota–immune axismicrobiota–inflammation pathwaygut–immune axisgut–systemic inflammation pathway
02

Mechanism of action

Modulation of microbial composition Enhancement or suppression of microbial metabolite (e.g., SCFAs) production Activation of host immune receptors (such as TLRs, GPRs, nuclear receptors) influencing cytokine production and T cell differentiation

03

Biological functions

Immune regulationInflammatory responseMaintenance of epithelial barrier integrityMetabolite signaling (e.g., SCFA, tryptophan metabolites)
04

Disease associations

InflammationAutoimmune diseaseCardiovascular diseaseObesityDiabetesNeurodegenerative diseases
05

Safety considerations

Unpredictable systemic effects of major alterations in microbiota composition (e.g., by FMT or antibiotics)Risk of pathogen transmission with microbiota-based therapiesLoss of colonization resistance to pathogensMetabolite imbalance may have off-target or pro-inflammatory consequences
06

Interacting drugs

Probiotics (e.g., Faecalibacterium prausnitzii, Roseburia)

4 more in the full profile.

07

Biomarkers

Microbial metabolite profiles (e.g., SCFAs, TMAO, tryptophan metabolites)Microbial taxonomic abundance (e.g., reduction of butyrate producers such as Faecalibacterium prausnitzii)Inflammatory cytokines (IL-6, TNF-α)Gut permeability markers

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