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Intermittent Fasting Confers Protection in CNS Autoimmunity by Altering the Gut Microbiota.


ABSTRACT: Multiple sclerosis (MS) is more common in western countries with diet being a potential contributing factor. Here we show that intermittent fasting (IF) ameliorated clinical course and pathology of the MS model, experimental autoimmune encephalomyelitis (EAE). IF led to increased gut bacteria richness, enrichment of the Lactobacillaceae, Bacteroidaceae, and Prevotellaceae families and enhanced antioxidative microbial metabolic pathways. IF altered T cells in the gut with a reduction of IL-17 producing T cells and an increase in regulatory T cells. Fecal microbiome transplantation from mice on IF ameliorated EAE in immunized recipient mice on a normal diet, suggesting that IF effects are at least partially mediated by the gut flora. In a pilot clinical trial in MS patients, intermittent energy restriction altered blood adipokines and the gut flora resembling protective changes observed in mice. In conclusion, IF has potent immunomodulatory effects that are at least partially mediated by the gut microbiome.

SUBMITTER: Cignarella F 

PROVIDER: S-EPMC6460288 | biostudies-literature | 2018 Jun

REPOSITORIES: biostudies-literature

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Intermittent Fasting Confers Protection in CNS Autoimmunity by Altering the Gut Microbiota.

Cignarella Francesca F   Cantoni Claudia C   Ghezzi Laura L   Salter Amber A   Dorsett Yair Y   Chen Lei L   Phillips Daniel D   Weinstock George M GM   Fontana Luigi L   Cross Anne H AH   Zhou Yanjiao Y   Piccio Laura L  

Cell metabolism 20180601 6


Multiple sclerosis (MS) is more common in western countries with diet being a potential contributing factor. Here we show that intermittent fasting (IF) ameliorated clinical course and pathology of the MS model, experimental autoimmune encephalomyelitis (EAE). IF led to increased gut bacteria richness, enrichment of the Lactobacillaceae, Bacteroidaceae, and Prevotellaceae families and enhanced antioxidative microbial metabolic pathways. IF altered T cells in the gut with a reduction of IL-17 pro  ...[more]

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