Mucosal microbial load in Crohn's disease: A potential predictor of response to faecal microbiota transplantation
Guillaume Sarrabayrouse,
Stefania Landolfi,
Marta Pozuelo,
Joseane Willamil,
Encarna Varela,
Allison Clark,
David Campos,
Claudia Herrera,
Alba Santiago,
Kathleen Machiels,
Severine Vermeire,
Marc Martí,
Eloy Espin,
Chaysavanh Manichanh
Affiliations
Guillaume Sarrabayrouse
Department of Gastroenterology, Vall d'Hebron Research Institute, Pg Vall d'Hebron, 119-129 Barcelona, Spain
Stefania Landolfi
Anatomical Pathology Department, Vall d'Hebron University Hospital, Barcelona, Spain
Marta Pozuelo
Department of Gastroenterology, Vall d'Hebron Research Institute, Pg Vall d'Hebron, 119-129 Barcelona, Spain
Joseane Willamil
Department of Gastroenterology, Vall d'Hebron Research Institute, Pg Vall d'Hebron, 119-129 Barcelona, Spain
Encarna Varela
Department of Gastroenterology, Vall d'Hebron Research Institute, Pg Vall d'Hebron, 119-129 Barcelona, Spain; CIBERehd, Instituto de Salud Carlos III, Madrid, Spain
Allison Clark
Department of Gastroenterology, Vall d'Hebron Research Institute, Pg Vall d'Hebron, 119-129 Barcelona, Spain
David Campos
Department of Gastroenterology, Vall d'Hebron Research Institute, Pg Vall d'Hebron, 119-129 Barcelona, Spain
Claudia Herrera
Department of Gastroenterology, Vall d'Hebron Research Institute, Pg Vall d'Hebron, 119-129 Barcelona, Spain
Alba Santiago
Department of Gastroenterology, Vall d'Hebron Research Institute, Pg Vall d'Hebron, 119-129 Barcelona, Spain
Kathleen Machiels
Department of Gastroenterology, University Hospital Gasthuisberg, Leuven, Belgium
Severine Vermeire
Department of Gastroenterology, University Hospital Gasthuisberg, Leuven, Belgium
Marc Martí
Unit of Colorectal Surgery, Department of General and Digestive Surgery, Vall d'Hebron University Hospital, Barcelona, Spain
Eloy Espin
Unit of Colorectal Surgery, Department of General and Digestive Surgery, Vall d'Hebron University Hospital, Barcelona, Spain
Chaysavanh Manichanh
Department of Gastroenterology, Vall d'Hebron Research Institute, Pg Vall d'Hebron, 119-129 Barcelona, Spain; CIBERehd, Instituto de Salud Carlos III, Madrid, Spain; Corresponding author at: Department of Gastroenterology, Vall d'Hebron Research Institute, Pg Vall d'Hebron, 119-129 Barcelona, Spain.
Background: The remission of Crohn's disease (CD) can be accomplished by faecal microbiota transplantation (FMT). However, this procedure has a low success rate, which could be attributed to mis-communication between recipient intestinal mucosa and donor microbiota. Methods: Here we used a human explant tissue model and an in vivo mouse model to examine changes in recipient intestinal mucosa upon contact with a faecal suspension (FS) obtained from a healthy donor. CD patients provided resected inflamed and non-inflamed mucosal tissues, whereas control colonic mucosa samples were collected from colorectal cancer patients. For the models, mucosal microbiome composition and tissue response were evaluated. Findings: We show that cytokine release and tissue damage were significantly greater in inflamed compared to non-inflamed CD tissues. Moreover, mucosal samples harbouring an initial low microbial load presented a shift in composition towards that of the FS, an increase in the relative count of Faecalibacterium prausnitzii, and a higher secretion of anti-inflammatory cytokine IL-10 compared to those with a high microbial load. Interpretation: Our results indicate that FMT during active inflammatory disease can compromise treatment outcome. We recommend the stratification of FMT recipients on the basis of tissue microbial load as a strategy to ensure successful colonization. Funding: This study was supported by grants from the Instituto de Salud Carlos III/FEDER (PI17/00614), the European Commission: (INCOMED-267128) and PERIS (SLT002/16). K.M. is a postdoctoral fellow and S.V. a senior clinical investigator of the Fund for Scientific Research Flanders, Belgium (FWO-Vlaanderen). Keywords: Intestinal microbiome, Crohn's disease, FMT, Recipient stratification, Microbial load, Anti-inflammatory cytokines