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Gut microbiome metabolites meet immunometabolism in inflammatory bowel disease

Trends in Immunology·June 23
ImmunologyLimited evidenceInflammatory Bowel DiseaseNarrative ReviewMetabolite TargetingMicrobiome-Based Therapy

Summary

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What was studied

This review examines how gut microbiota-derived metabolites regulate immunometabolism in IBD, focusing on their roles in reshaping mitochondrial function, cellular metabolic pathways, and immune cell behavior in the context of dysbiosis.

Key findings

Microbial metabolites act as key intermediates in host-microbe communication; dysbiosis can perturb immune homeostasis by rewiring host metabolic circuits, and targeting the microbiota-metabolite-immunometabolism axis is proposed as a promising therapeutic strategy in IBD.

Study limitations

As a review, no original clinical or experimental data are presented; the therapeutic concepts discussed are largely preclinical and described as 'underexplored,' limiting direct clinical applicability.

Clinical implications

Clinicians managing IBD should watch this space: the microbiota-metabolite-immunometabolism axis is emerging as a novel therapeutic target, though interventions remain investigational and are not yet ready for routine clinical use.

Related Questions

Explore related topics

How do short-chain fatty acids regulate immune cell metabolism in IBD?What microbiome metabolites are dysregulated in Crohn's disease and ulcerative colitis?Are there clinical trials targeting the gut microbiota-immunometabolism axis in IBD?

Publication Details

Year
2026
Journal
Trends in Immunology
Source
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