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Third-party fecal microbiota transplantation for high-risk treatment-naïve acute GVHD of the lower GI tract

粪便细菌疗法 粪便 移植 医学 内科学 胃肠病学 肠道菌群 胃肠道 免疫学 生物 微生物学 抗生素 艰难梭菌
作者
Zachariah DeFilipp,Ashish Damania,Haesook T. Kim,Chia‐Chi Chang,Areej El‐Jawahri,Steven L. McAfee,AJ S. Bottoms,Vesselina Toncheva,Melissa Smith,Maria Dolaher,Lindsey S. Perry,Meghan White,Brittany Diana,Sheila Connolly,Bimalangshu R. Dey,Matthew J. Frigault,Richard Newcomb,Paul V. O’Donnell,Thomas R. Spitzer,Michael K. Mansour,Daniela Weber,Nadim J. Ajami,Elizabeth Hohmann,Robert R. Jenq,Yi-Bin Chen
出处
期刊:Blood Advances [Elsevier BV]
标识
DOI:10.1182/bloodadvances.2024012556
摘要

Disruption of the intestinal microbiome is observed with acute graft-versus-host disease (GVHD) of the lower gastrointestinal (LGI) tract and fecal microbiota transplantation (FMT) has successfully cured steroid-refractory cases. In this open-label, single-arm, pilot study (NCT04139577), third-party, single donor FMT was administered in combination with systemic corticosteroids to participants with high-risk acute LGI GVHD, with a focus on treatment-naïve cases. Participants were scheduled to receive one induction dose (15 capsules/day for 2 consecutive days), followed by 3 weekly maintenance doses, consisting of 15 capsules/dose. The primary endpoint of the study was feasibility, which would be achieved if ≥80% of participants able to swallow ≥40 of the 75 scheduled capsules. Ten participants (9 treatment-naïve; 1 steroid-refractory) were enrolled and treated. The study met the primary endpoint, with 9 of 10 participants completing all eligible doses. Organ-specific LGI complete response rate at Day 28 was 70%. Initial clinical response was observed within 1 week for all responders and clinical responses were durable, without recurrent LGI GVHD in complete responders. Exploratory analyses suggest that alpha diversity increased following FMT. While recipient microbiome composition never achieved a high degree of donor similarity, expansion of donor-derived species and increases in tryptophan metabolites and short-chain fatty acids were observed within the first 7 days after FMT. Investigation into the use of microbiome-targeted interventions earlier in the treatment paradigm for acute LGI GVHD is warranted.

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