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Human Gut-Derived Commensal Bacteria Suppress CNS Inflammatory and Demyelinating Disease
Journal article   Open access   Peer reviewed

Human Gut-Derived Commensal Bacteria Suppress CNS Inflammatory and Demyelinating Disease

Ashutosh K Mangalam, Shailesh K Shahi, David Luckey, Melissa Karau, Eric Marietta, Ningling Luo, Rok Seon Choung, Josephine Ju, Ramakrishna Sompallae, Katherine Gibson-Corley, …
Cell Reports, Vol.20(6), pp.1269-1277
08/08/2017
DOI: 10.1016/j.celrep.2017.07.031
PMCID: PMC5763484
PMID: 28793252
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Published (Version of record)CC BY-NC-ND V4.0 Open Access
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https://doi.org/10.1016/j.celrep.2017.07.031View
Published (Version of record)Cell Reports 20, 1269–1277.

Abstract

The human gut is colonized by a large number of microorganisms (∼1013 bacteria) that support various physiologic functions. A perturbation in the healthy gut microbiome might lead to the development of inflammatory diseases, such as multiple sclerosis (MS). Therefore, gut commensals might provide promising therapeutic options for treating MS and other diseases. We report the identification of human gut-derived commensal bacteria, Prevotella histicola, which can suppress experimental autoimmune encephalomyelitis (EAE) in a human leukocyte antigen (HLA) class II transgenic mouse model. P. histicola suppresses disease through the modulation of systemic immune responses. P. histicola challenge led to a decrease in pro-inflammatory Th1 and Th17 cells and an increase in the frequencies of CD4+FoxP3+ regulatory T cells, tolerogenic dendritic cells, and suppressive macrophages. Our study provides evidence that the administration of gut commensals may regulate a systemic immune response and may, therefore, have a possible role in treatment strategies for MS.

Gastroenterology Hepatology Inflammation Medical Microbiology Multiple Sclerosis Pathology Immune System Diseases OAfund EAE Prevotella histicola demyelination experimental autoimmune encephalomyelitis gut microbiome human commensal immunomodulation regulatory T cells

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