Microbiota therapeutics for inflammatory bowel disease: the way forward
- PMID: 38604201
- DOI: 10.1016/S2468-1253(23)00441-7
Microbiota therapeutics for inflammatory bowel disease: the way forward
Abstract
Microbiota therapeutics that transplant faecal material from healthy donors to people with mild-to-moderate ulcerative colitis have shown the potential to induce remission in about 30% of participants in small, phase 2 clinical trials. Despite this substantial achievement, the field needs to leverage the insights gained from these trials and progress towards phase 3 clinical trials and drug approval, while identifying the distinct clinical niche for this new therapeutic modality within inflammatory bowel disease (IBD) therapeutics. We describe the lessons that can be learned from past studies of microbiota therapeutics, from full spectrum donor stool to defined products manufactured in vitro. We explore the actionable insights these lessons provide on the design of near-term studies and future trajectories for the integration of microbiota therapeutics in the treatment of IBD. If successful, microbiota therapeutics will provide a powerful orthogonal approach (complementing or in combination with existing immunomodulatory drugs) to raise the therapeutic ceiling for the many non-responders and partial responders within the IBD patient population.
Copyright © 2024 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of interests J-FC reports research grants from AbbVie, Janssen Pharmaceuticals, Takeda, and Bristol Myers Squibb; payment for lectures from AbbVie and Takeda; consulting fees from AbbVie, Amgen, AnaptysBio, Allergan, Arena Pharmaceuticals, Boehringer Ingelheim, Bristol Myers Squibb, Celgene Corporation, Celltrion, Eli Lilly, Ferring Pharmaceuticals, Galmed Research, Glaxo Smith Kline, Genentech (Roche), Janssen Pharmaceuticals, Kaleido Biosciences, Immunic, Invea, Iterative Scopes, Merck, Landos, Microba Life Science, Novartis, Otsuka Pharmaceutical, Pfizer, Protagonist Therapeutics, Prometheus, Sanofi, Seres, Takeda, Teva, TiGenix, and Vifor; and stock options in Intestinal Biotech Development. FM has served as a speaker and received honoraria from Merck Sharp & Dohme, Abbvie, Vifor, Falk, Laboratórios Vitória, Pfizer, Ferring, Hospira, Biogen, Eli Lilly, OM Pharma, PharmaKern, Schering, Sandoz, and Takeda. AG reports consulting fees from Aimmune Therapeutics and Ferring Therapeutics. JJF reports research grants from Janssen Pharmaceuticals. JJF has consulted for Seed Health, Innovation Pharmaceuticals, and Vedanta Biosciences; and is a scientific advisory board member of Vedanta Biosciences. JJF received funding from the National Institutes of Health (grant numbers DK124133, DK130337, and DK112978) and from the Crohn's & Colitis Foundation Litwin IBD Pioneers Award. JJF and LB have patents related to microbial therapeutics. MME declares no competing interests.
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