Donor fecal microbiota transplantation ameliorates intestinal graft-versus-host disease in allogeneic hematopoietic cell transplant recipients.
Yannouck F van LierMark DavidsNienke J E HaverkatePieter F de GrootMarjolein L DonkerEllen MeijerFloor C J I Heubel-MoenenErfan NurSacha S ZeerlederMax NieuwdorpBianca BlomMette D HazenbergPublished in: Science translational medicine (2021)
Disruption of the intestinal microbiota occurs frequently in allogeneic hematopoietic cell transplantation (allo-HCT) recipients and predisposes them to development of graft-versus-host disease (GvHD). In a prospective, single-center, single-arm study, we investigated the effect of donor fecal microbiota transplantation (FMT) on symptoms of steroid-refractory or steroid-dependent, acute or late-onset acute intestinal GvHD in 15 individuals who had undergone allo-HCT. Study participants received a fecal suspension from an unrelated healthy donor via nasoduodenal infusion. Donor FMT was well tolerated, and infection-related adverse events did not seem to be related to the FMT procedure. In 10 of 15 study participants, a complete clinical response was observed within 1 month after FMT, without additional interventions to alleviate GvHD symptoms. This response was accompanied by an increase in gut microbial α-diversity, a partial engraftment of donor bacterial species, and increased abundance of butyrate-producing bacteria, including Clostridiales and Blautia species. In 6 of the 10 responding donor FMT recipients, immunosuppressant drug therapy was successfully tapered. Durable remission of steroid-refractory or steroid-dependent GvHD after donor FMT was associated with improved survival at 24 weeks after donor FMT. This study highlights the potential of donor FMT as a treatment for steroid-refractory or steroid-dependent GvHD, but larger clinical trials are needed to confirm the safety and efficacy of this procedure.
Keyphrases
- late onset
- clinical trial
- bone marrow
- emergency department
- early onset
- allogeneic hematopoietic stem cell transplantation
- cell therapy
- low dose
- mouse model
- single cell
- signaling pathway
- acute myeloid leukemia
- mesenchymal stem cells
- open label
- high resolution
- cell proliferation
- single molecule
- acute respiratory distress syndrome
- pi k akt
- cord blood
- atomic force microscopy