Fecal microbiota transplantation in capsules for the treatment of steroid refractory and steroid dependent acute graft vs. host disease: a pilot study

Ilan Youngster, Adi Eshel, Mika Geva, Ivetta Danylesko, Israel Henig, Tsila Zuckerman, Shalev Fried, Ronit Yerushalmi, Noga Shem-Tov, Joshua A. Fein, David Bomze, Avichai Shimoni, Omry Koren, Roni Shouval, Arnon Nagler

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Acute graft-versus-host disease (aGvHD) is a serious complication of allogeneic hematopoietic stem-cell transplantation with limited treatment options. The gut microbiome plays a critical role in aGvHD pathogenesis. Fecal microbiota transplantation (FMT) has emerged as a potential therapeutic approach to restore gut microbial diversity. In this prospective pilot study, 21 patients with steroid-resistant or steroid-dependent lower gastrointestinal aGvHD received FMT in capsule form. At 28 days after the first FMT, the overall response rate was 52.4%, with 23.8% complete and 28.6% partial responses. However, sustained responses were infrequent, with only one patient remaining aGvHD-free long-term. FMT was generally well-tolerated. Microbiome analysis revealed dysbiosis in pre-FMT patient stool samples, with distinct microbial characteristics compared to donors. Following FMT, there was an increase in beneficial Clostridiales and a decrease in pathogenic Enterobacteriales. These findings highlight the potential of FMT as a treatment option for steroid-resistant aGvHD. Trial registration number NCT #03214289.

Original languageEnglish
Pages (from-to)409-416
Number of pages8
JournalBone Marrow Transplantation
Volume59
Issue number3
Early online date11 Jan 2024
DOIs
StatePublished - Mar 2024

Bibliographical note

Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Limited 2024.

Funding

RS was supported by Memorial Sloan Kettering Cancer Center Core grant (P30 CA008748) from the National Institutes of Health/National Cancer Institute and by an NIH-NCI K-award (K08CA282987). The study was supported by the Dahlia Greidinger Anti Cancer Fund, the Gassner Fund for Medical Research, and an institutional grant from the Chaim Sheba Medical Center.

FundersFunder number
Gassner Fund for Medical Research
National Institutes of Health
National Cancer InstituteK08CA282987
Dahlia Greidinger Anti-Cancer Fund
Sheba Medical Center

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