Targeting the gut microbiome in inflammatory bowel disease: from concept to clinical reality

28 - Octobre - 2025

Nathalie Rolhion, Harry Sokol

Intest Res. 2025 Oct;23(4):396-404


ABSTRACT:

The gut microbiota, a complex community of trillions of microorganisms inhabiting the human gastrointestinal tract, has emerged as a critical regulator of immune homeostasis and gastrointestinal health. In the context of inflammatory bowel disease (IBD), comprising primarily Crohn's disease and ulcerative colitis, disruptions to this microbial ecosystem-collectively termed dysbiosis-have been increasingly recognized as central to disease pathogenesis. Recent research has established that alterations in gut microbiota not only reflect disease states but may actively drive immune dysregulation, barrier dysfunction, and mucosal inflammation. This review synthesizes current knowledge on the role of the gut microbiota in IBD and evaluates the therapeutic landscape of microbiota-modulating strategies using selected examples. Fecal microbiota transplantation, while offering proof-of-concept validation, is hindered by standardization challenges and variable clinical outcomes. As a response, microbiome-based therapeutics have evolved toward defined live biotherapeutic products including bacterial consortia and single-strain products, postbiotics, and metabolite-centered approaches targeting specific pathways. Groundbreaking research into rationally designed synthetic microbiomes and next-generation probiotics is driving a paradigm shift in microbiota-based treatment for IBD from empirical to precision-guided interventions.

Different types of strategies to target the gut microbiota in inflammatory bowel disease (IBD). FMT, fecal microbiota transplantation; LBP, live biotherapeutic product; AIEC, adherent-invasive Escherichia coli.Mechanisms underlying the anti-inflammatory effects of Faecalibacterium prausnitzii. MAM, microbial anti-inflammatory molecule; NF-kB, nuclear factor-kappa B; IL-10, interleukin 10.

 

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