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McMaster Team Uses Phages to Disarm Crohn’s‑Linked E. coli

Targeted phages suppressed a bacterial attachment mechanism that drives inflammation, suggesting a biomarker‑guided path toward human trials.

Overview

  • McMaster researchers published peer‑reviewed results on July 8, 2026 showing bacteriophages that target adherent‑invasive E. coli (AIEC) reduced gut inflammation in controlled preclinical models.
  • The phages did not eradicate the bacteria but switched off a genetic promoter (fimS) that controls the FimH adhesion 'grappling hook', preventing bacterial attachment and lowering immune activation.
  • A single phage, HER259, relieved colitis in gnotobiotic mouse models but stopping treatment allowed the fimS promoter to revert and inflammation to return.
  • When paired with a common corticosteroid, the phage allowed researchers to use a lower drug dose while preserving therapeutic benefit, indicating potential for dose‑sparing and fewer steroid side effects.
  • The targeted bacterial function is measurable in stool and is enriched in a subset of Crohn’s patients, and the team plans broader strain surveys, phage cocktail development, biomarker validation, and steps toward human trials.