Jacob Vinita, Crawford Carl, Cohen-Mekelburg Shirley, Viladomiu Monica, Putzel Gregory G, Schneider Yecheskel, Chabouni Fatiha, OʼNeil Sarah, Bosworth Brian, Woo Viola, Ajami Nadim J, Petrosino Joseph F, Gerardin Ylaine, Kassam Zain, Smith Mark, Iliev Iliyan D, Sonnenberg Gregory F, Artis David, Scherl Ellen, Longman Randy S
*Jill Roberts Center for IBD, Weill Cornell Medicine, New York, New York; †Division of Gastroenterology and Hepatology, Weill Cornell Medicine, New York, New York; ‡Jill Roberts Institute for Research in IBD, Weill Cornell Medicine, New York, New York; §Department of Medicine, NYU School of Medicine, New York, New York; ‖Alkek Center for Metagenomics and Microbiome Research, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas; ¶Finch Therapeutics, Somerville, Massachusetts; and **OpenBiome, Medford, Massachusetts.
Inflamm Bowel Dis. 2017 Jun;23(6):903-911. doi: 10.1097/MIB.0000000000001132.
Recent trials suggest fecal microbiota transplantation (FMT) with repeated enemas and high-diversity FMT donors is a promising treatment to induce remission in ulcerative colitis.
We designed a prospective, open-label pilot study to assess the safety, clinical efficacy, and microbial engraftment of single FMT delivery by colonoscopy for active ulcerative colitis using a 2-donor fecal microbiota preparation (FMP). Safety and clinical endpoints of response, remission, and mucosal healing at week 4 were assessed. Fecal DNA and rectal biopsies were used to characterize the microbiome and mucosal CD4 T cells, respectively, before and after FMT.
Of the 20 patients enrolled in this study, 7 patients (35%) achieved a clinical response by week 4. Three patients (15%) were in remission at week 4 and 2 of these patients (10%) achieved mucosal healing. Three patients (15%) required escalation of care. No serious adverse events were observed. Microbiome analysis revealed that restricted diversity of recipients pre-FMT was significantly increased by high-diversity 2-donor FMP. The microbiome of recipients post-transplant was more similar to the donor FMP than the pretransplant recipient sample in both responders and nonresponders. Notably, donor composition correlated with clinical response. Mucosal CD4 T-cell analysis revealed a reduction in both Th1 and regulatory T-cells post-FMT.
High-diversity, 2-donor FMP delivery by colonoscopy seems safe and effective in increasing fecal microbial diversity in patients with active ulcerative colitis. Donor composition correlated with clinical response and further characterization of immunological parameters may provide insight into factors influencing clinical outcome.
近期试验表明,采用重复灌肠和高多样性粪便微生物群移植(FMT)供体进行粪便微生物群移植是诱导溃疡性结肠炎缓解的一种有前景的治疗方法。
我们设计了一项前瞻性、开放标签的试点研究,以评估使用双供体粪便微生物群制剂(FMP)通过结肠镜检查单次FMT治疗活动性溃疡性结肠炎的安全性、临床疗效和微生物植入情况。评估了第4周时反应、缓解和黏膜愈合的安全性及临床终点。分别在FMT前后,使用粪便DNA和直肠活检来表征微生物群和黏膜CD4 T细胞。
本研究纳入的20例患者中,7例患者(35%)在第4周时获得临床反应。3例患者(15%)在第4周时处于缓解状态,其中2例患者(10%)实现黏膜愈合。3例患者(15%)需要加强治疗。未观察到严重不良事件。微生物群分析显示,高多样性双供体FMP显著增加了FMT前受体受限的多样性。在反应者和无反应者中,移植后受体的微生物群比移植前受体样本更类似于供体FMP。值得注意的是,供体组成与临床反应相关。黏膜CD4 T细胞分析显示,FMT后Th1细胞和调节性T细胞均减少。
通过结肠镜检查递送高多样性、双供体FMP似乎对增加活动性溃疡性结肠炎患者的粪便微生物多样性是安全有效的。供体组成与临床反应相关,进一步表征免疫参数可能有助于深入了解影响临床结果的因素。