DOI: 10.1126/scitranslmed.aee3263 ISSN: 1946-6234

Fecal microbiome transplant in food allergy in humans and mice identifies a role for bile acid metabolites in oral tolerance

Rima Rachid, Monica Martinez-Blanco, Gavin A. Kuziel, Emmanuel Stephen-Victor, Mathieu Groussin, Askarbek Orakov, George Russell, Le Thanh Tu Nguyen, Mathilde Poyet, Zhussipbek Mukhatayev, Christina S. K. Yee, Sultan Albuhairi, Rayan Kteish, Ebla Abdel Rahman, Farida Abi Farraj, Ziwei Wang, Suzanne Dahlberg, Morgan Ryan, Meghan Fitzgerald, Wendy Elverson, John J. Lee, Lynda Schneider, Andrew MacGinnitie, Elena Crestani, Dianna Queheillalt, Elizabeth Burke-Roberts, Jonathan Watson, Ryan J. Elliott, Wing Fei Wong, Majdi Osman, Robert Voyksner, Elizabeth Hohmann, Curtis Huttenhower, Eric Alm, Seth Rakoff-Nahoum, Talal A. Chatila

The gut microbiome has been implicated in the pathogenesis of food allergy (FA), prompting microbiome-focused interventions. We evaluated, in a phase 1 open-label trial (NCT02960074), the safety and efficacy of oral encapsulated fecal microbiome transplantation (FMT) in 15 adults with peanut allergies. An increase in the peanut reactivity threshold was noted in 3 of 10 participants not pretreated with antibiotics and 3 of 5 participants pretreated with antibiotics, without safety issues. In responders, FMT increased tolerogenic RORγt + regulatory T cells (T reg cells) and decreased T helper 2 cells (T H 2 cells). Mice transplanted with the microbiomes of post-FMT responders were protected from FA in association with increased RORγt + T reg cell percentages and increased colonization with members of the gut Bacteroides . In both humans and mice, protection by FMT was associated with increased bile acid metabolites. Deletion of a bile salt hydrolase in a candidate protective Bacteroides abrogated FA suppression in mice. These results suggest that FMT is a safe and potentially promising therapeutic modality for treating FA.

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