Fecal Microbiota Transfer

Andreas Stallmach1, Arndt Steube, Philip Grunert

  • 1Department of Internal Medicine IV (Gastroenterology, Hepatology, Infectious Diseases), Jena University Hospital, Jena, Germany; University Pharmacy, Jena University Hospital, Jena, Germany; University of Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen, Bonn, Cologne, Duesseldorf, Germany; German Centre for Infection Research (DZIF), partner site Bonn-Cologne, Germany; Department of Internal Medicine, Infectious Diseases, University Hospital Frankfurt, Goethe University Frankfurt, Frankfurt am Main, Germany.

Abstract

Insights

Fecal microbiota transfer (FMT) is highly effective for recurrent Clostridioides difficile infection (rCDI). Encapsulated, frozen microbiota offers a standardized and safe treatment option for patients with rCDI.

Area of Science:

  • Microbiology
  • Gastroenterology
  • Infectious Diseases

Background:

  • Fecal microbiota transfer (FMT) is increasingly utilized globally for treating recurrent Clostridioides difficile infection (rCDI).
  • FMT is performed for research and individual patient treatment outside clinical trials.
  • Lack of standardized protocols for donor screening and fecal transfer methods poses potential risks.

Purpose of the Study:

  • To review the efficacy and safety of FMT for rCDI.
  • To establish best practices for FMT procedures.
  • To identify optimal methods for fecal microbiota administration.

Main Methods:

  • Selective literature search including consensus conference reports.
  • Review of studies on donor screening, FMT methods, and patient outcomes.
  • Analysis of data on efficacy and adverse events.

Main Results:

  • FMT is the preferred treatment for rCDI due to high efficacy.
  • FMT is generally safe, even in immunocompromised patients, with proper donor screening.
  • Oral ingestion of frozen, encapsulated microbiota is as effective as other delivery methods for rCDI.

Conclusions:

  • Encapsulated fecal microbiome (FM) stored at -20°C is the preferred method due to standardization and quality control.
  • Patients with rCDI should receive FMT via oral capsules.
  • Research is ongoing to identify active components of FM and explore recombinant production.