Abstract

Fecal Microbiota Transplant (FMT) has shown some success in treating inflammatory bowel diseases (IBD). There is emerging evidence that host engraftment of donor taxa is a tenet of successful FMT. We undertook a double-blind, randomized, placebo-controlled pilot study to characterize the response to FMT in children and young adults with mild to moderate active Crohn’s disease (CD) and ulcerative colitis (UC). Subjects with CD or UC were randomized to receive antibiotics and weekly FMT or placebo in addition to baseline medications. We enrolled 15 subjects aged 14–29 years. Four subjects had CD, and 11 had UC. Subjects exhibited a wide range of microbial diversity and donor engraftment. Specifically, engraftment ranged from 26 to 90% at week 2 and 3–92% at 2 months. Consistent with the current literature, increases over time of both alpha diversity (p < 0.05) and donor engraftment (p < 0.05) correlated with improved clinical response. We discovered that the post-antibiotic but pre-FMT time point was rich in microbial correlates of eventual engraftment. Greater residual alpha diversity after antibiotic treatment was positively correlated with engraftment and subsequent clinical response. Interestingly, a transient rise in the relative abundance of Lactobacillus was also positively correlated with engraftment, a finding that we recapitulated with our analysis of another FMT trial.

Details

Title
Higher alpha diversity and Lactobacillus blooms are associated with better engraftment after fecal microbiota transplant in inflammatory bowel disease
Author
Zhang, Yanjia Jason 1 ; Bousvaros, Athos 2 ; Docktor, Michael 3 ; Kaplan, Abby L. 3 ; Rufo, Paul A. 3 ; Leier, McKenzie 3 ; Weatherly, Madison 3 ; Zimmerman, Lori 3 ; Nguyen, Le Thanh Tu 4 ; Barton, Brenda 5 ; Russell, George 6 ; Alm, Eric J. 4 ; Kahn, Stacy A. 3 

 Boston Children’s Hospital, Gastroenterology/Nutrition, Boston, USA (GRID:grid.2515.3) (ISNI:0000 0004 0378 8438); Massachusetts Institute of Technology, Department of Biological Engineering, Cambridge, USA (GRID:grid.116068.8) (ISNI:0000 0001 2341 2786); Massachusetts Institute of Technology, Center for Microbiome Informatics and Therapeutics, Cambridge, USA (GRID:grid.116068.8) (ISNI:0000 0001 2341 2786) 
 Boston Children’s Hospital, Gastroenterology/Nutrition, Boston, USA (GRID:grid.2515.3) (ISNI:0000 0004 0378 8438); Massachusetts Institute of Technology, Center for Microbiome Informatics and Therapeutics, Cambridge, USA (GRID:grid.116068.8) (ISNI:0000 0001 2341 2786) 
 Boston Children’s Hospital, Gastroenterology/Nutrition, Boston, USA (GRID:grid.2515.3) (ISNI:0000 0004 0378 8438); Boston Children’s Hospital, IBD Center, Boston, USA (GRID:grid.2515.3) (ISNI:0000 0004 0378 8438) 
 Massachusetts Institute of Technology, Department of Biological Engineering, Cambridge, USA (GRID:grid.116068.8) (ISNI:0000 0001 2341 2786); Massachusetts Institute of Technology, Center for Microbiome Informatics and Therapeutics, Cambridge, USA (GRID:grid.116068.8) (ISNI:0000 0001 2341 2786) 
 Boston Children’s Hospital, Gastroenterology/Nutrition, Boston, USA (GRID:grid.2515.3) (ISNI:0000 0004 0378 8438) 
 Maine Medical Center, Gastroenterology/Nutrition, Portland, USA (GRID:grid.240160.1) 
Pages
18188
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3089709575
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.