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April 26, 2026Biomedicines2 citationsOpen Access

Microbiome-Based Therapies in Ulcerative Colitis: Mechanisms, Clinical Evidence, and a Precision-Medicine Framework

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PPPhilippe Pinton

Key Points

  • This review aims to explore the efficacy and mechanisms of microbiome-based therapies in managing ulcerative colitis.
  • Synthesis of findings from randomized controlled trials and early-phase studies on microbiome interventions.
  • Analysis of various therapeutic approaches, including fecal microbiota transplantation and defined microbial consortia.
  • Integration of clinical evidence with patient-specific microbial profiles for therapy selection.
  • Fecal microbiota transplantation showed significant improvements in microbial diversity and UC remission rates.
  • Defined microbial consortia demonstrated targeted outcomes in metabolic pathways and immune responses.
  • Broader mechanistic coverage in consortia correlated with consistent biological activity compared to narrow designs.

Abstract

Microbiome-based therapies are reshaping the therapeutic landscape for ulcerative colitis (UC), offering new avenues for disease management beyond conventional immunomodulatory and biologic treatments. UC remains a chronic, relapsing condition with significant unmet clinical needs, as many patients fail to achieve sustained remission or experience adverse effects with current therapies. The gut microbiome has emerged as a central contributor to UC pathogenesis, influencing epithelial barrier integrity, immune homeostasis, and metabolic signaling. Interventions such as fecal microbiota transplantation (FMT) and defined microbial consortia have demonstrated proof-of-concept efficacy in early-phase clinical trials, each leveraging distinct mechanistic strategies. FMT, as a broad ecological intervention, restores microbial diversity and functional redundancy, potentially addressing multiple pathogenic mechanisms simultaneously. In contrast, defined consortia enable precise targeting of specific metabolic and immunological pathways, including short-chain fatty acid production, bile-acid remodeling, epithelial barrier reinforcement, immune modulation, and succinate degradation. Recent clinical evidence suggests that consortia with broader mechanistic coverage may achieve more consistent biological activity than narrowly focused designs. This review synthesizes mechanistic and clinical insights across broad and defined microbial consortia, integrates evidence from randomized controlled trials and early-phase LBP studies, and outlines a precision-medicine framework to guide therapy selection. We highlight the importance of aligning therapeutic mechanisms with patient-specific microbial, metabolic, and immune profiles, and discuss future directions including biomarker-guided stratification, hybrid consortia, and adaptive trial designs. Advancing both broad and defined approaches, while incorporating ecological principles, mechanistic understanding, and patient stratification, will be essential to realizing the full therapeutic potential of microbiome-based therapies in UC.

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Philippe Pinton (2026) studied this question.

synapsesocial.com/papers/69edad8f4a46254e215b51echttps://doi.org/10.3390/biomedicines14050969
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