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.
Journal article
Human Gut-Derived Commensal Bacteria Suppress CNS Inflammatory and Demyelinating Disease
Cell Reports, Vol.20(6), pp.1269-1277
08/08/2017
DOI: 10.1016/j.celrep.2017.07.031
PMCID: PMC5763484
PMID: 28793252
Abstract
Details
- Title: Subtitle
- Human Gut-Derived Commensal Bacteria Suppress CNS Inflammatory and Demyelinating Disease
- Creators
- Ashutosh K Mangalam - University of IowaShailesh K Shahi - University of IowaDavid Luckey - Mayo ClinicMelissa Karau - Mayo ClinicEric Marietta - Mayo ClinicNingling Luo - Mayo ClinicRok Seon Choung - Mayo ClinicJosephine Ju - Mayo ClinicRamakrishna Sompallae - University of IowaKatherine Gibson-Corley - University of IowaRobin Patel - Mayo ClinicMoses Rodriguez - Mayo ClinicChella David - Mayo ClinicVeena Taneja - Mayo ClinicJoseph Murray - Mayo Clinic
- Resource Type
- Journal article
- Publication Details
- Cell Reports, Vol.20(6), pp.1269-1277
- DOI
- 10.1016/j.celrep.2017.07.031
- PMID
- 28793252
- PMCID
- PMC5763484
- NLM abbreviation
- Cell Rep
- ISSN
- 2211-1247
- Number of pages
- 9
- Copyright
- Copyright © 2017 The Authors
- Grant note
- Funder: 3M, Merck, Allergan, Infectious Diseases Society of America, National Institutes of Health (NS048357, GM092993, NS073684), European Regional Development Fund (FNUSA-ICRC CZ.1.05/1.1.00/02.0123), Hilton, Department of Defense (DOD) (W81XWH-10-1-0254), National Multiple Sclerosis Society (NMSS) (RG 5138A1/1T), BioFire, Check-Points, Curetis, Hutchison Biofilm Medical Solutions, Accelerate Diagnostics, The Medicines Company, ASM, USMLE, Up-to-Date, Infectious Diseases Board Review Course, NIH CTSA (RR024150, TR000135), Novartis Pharmaceuticals, Applebaum, Peterson, McNeilus Foundations, Grant ID: DOD W81XWH- 10-1-0254, NMSS RG 5138A1/1T, NIH GM092993, NS048357, NS073684, NIH CTSA RR024150 and TR000135, ERDF FNUSA-ICRC CZ.1.05/1.1.00/ 02.0123
- Language
- English
- Date published
- 08/08/2017
- Academic Unit
- Pathology; Iowa Neuroscience Institute; Ophthalmology and Visual Sciences
- Record Identifier
- 9983557487502771
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