Faecal Microbiota Transplantation Engraftment After Budesonide or Placebo in Patients With Active Ulcerative Colitis Using Pre-selected Donors: A Randomized Pilot Study

Author:

van Lingen Emilie1,Nooij Sam2,Terveer Elisabeth M2,Crossette Emily3,Prince Amanda L3,Bhattarai Shakti K4,Watson Andrea3,Galazzo Gianluca3,Menon Rajita3,Szabady Rose L35,Bucci Vanni4,Norman Jason M3,van der Woude C Janneke6,van der Marel Sander7,Verspaget Hein W1,van der Meulen-de Jong Andrea E1,Keller Josbert J17

Affiliation:

1. Department of Gastroenterology and Hepatology, Leiden University Medical Center , Leiden , The Netherlands

2. Department of Medical Microbiology, Leiden University Medical Center , Leiden , The Netherlands

3. Vedanta Biosciences , Cambridge, MA , USA

4. University of Massachusetts Chan Medical School, Department of Microbiology and Physiological Systems , Worcester, MA , USA

5. Ferring Pharmaceuticals , San Diego, CA , USA

6. Department of Gastroenterology and Hepatology, Erasmus Medical Center , Rotterdam , The Netherlands

7. Department of Gastroenterology and Hepatology , Haaglanden Medisch Centrum, den Haag , The Netherlands

Abstract

Abstract Background Faecal microbiota transplantation [FMT] shows some efficacy in treating patients with ulcerative colitis [UC], although variability has been observed among donors and treatment regimens. We investigated the effect of FMT using rationally selected donors after pretreatment with budesonide or placebo in active UC. Methods Patients ≥18 years old with mild to moderate active UC were randomly assigned to 3 weeks of budesonide [9 mg] or placebo followed by 4-weekly infusions of a donor faeces suspension. Two donors were selected based on microbiota composition, regulatory T cell induction and short-chain fatty acid production in mice. The primary endpoint was engraftment of donor microbiota after FMT. In addition, clinical efficacy was assessed. Results In total, 24 patients were enrolled. Pretreatment with budesonide did not increase donor microbiota engraftment [p = 0.56] nor clinical response, and engraftment was not associated with clinical response. At week 14, 10/24 [42%] patients achieved [partial] remission. Remarkably, patients treated with FMT suspensions from one donor were associated with clinical response [80% of responders, p < 0.05] but had lower overall engraftment of donor microbiota. Furthermore, differences in the taxonomic composition of the donors and the engraftment of certain taxa were associated with clinical response. Conclusion In this small study, pretreatment with budesonide did not significantly influence engraftment or clinical response after FMT. However, clinical response appeared to be donor-dependent. Response to FMT may be related to transfer of specific strains instead of overall engraftment, demonstrating the need to characterize mechanisms of actions of strains that maximize therapeutic benefit in UC.

Funder

Vedanta Biosciences

Publisher

Oxford University Press (OUP)

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