| Literature DB >> 28793252 |
Ashutosh Mangalam1, Shailesh K Shahi2, David Luckey3, Melissa Karau4, Eric Marietta5, Ningling Luo3, Rok Seon Choung5, Josephine Ju6, Ramakrishna Sompallae7, Katherine Gibson-Corley2, Robin Patel4, Moses Rodriguez8, Chella David3, Veena Taneja3, Joseph Murray9.
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.Entities:
Keywords: EAE; Prevotella histicola; demyelination; experimental autoimmune encephalomyelitis; gut microbiome; human commensal; immunomodulation; inflammation; multiple sclerosis; regulatory T cells
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Year: 2017 PMID: 28793252 PMCID: PMC5763484 DOI: 10.1016/j.celrep.2017.07.031
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423