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dc.contributor.authorFox, James G.
dc.contributor.authorGe, Zhongming
dc.contributor.authorWhary, Mark T.
dc.contributor.authorErdman, Susan E.
dc.contributor.authorHorwitz, Bruce H.
dc.date.accessioned2014-08-15T14:28:40Z
dc.date.available2014-08-15T14:28:40Z
dc.date.issued2010-10
dc.date.submitted2010-06
dc.identifier.issn1933-0219
dc.identifier.issn1935-3456
dc.identifier.urihttp://hdl.handle.net/1721.1/88710
dc.description.abstractPioneering work in the 1990s first linked a novel microaerobic bacterium, Helicobacter hepaticus, with chronic active hepatitis and inflammatory bowel disease in several murine models. Targeted H. hepaticus infection experiments subsequently demonstrated its ability to induce colitis, colorectal cancer, and extraintestinal diseases in a number of mouse strains with defects in immune function and/or regulation. H. hepaticus is now widely utilized as a model system to dissect how intestinal microbiota interact with the host to produce both inflammatory and tolerogenic responses. This model has been used to make important advances in understanding factors that regulate both acquired and innate immune response within the intestine. Further, it has been an effective tool to help define the function of regulatory T cells, including their ability to directly inhibit the innate inflammatory response to gut microbiota. The complete genomic sequence of H. hepaticus has advanced the identification of several virulence factors and aided in the elucidation of H. hepaticus pathogenesis. Delineating targets of H. hepaticus virulence factors could facilitate novel approaches to treating microbially induced lower bowel inflammatory diseases.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant R01-DK052413)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant P01-CA026731)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant R01-CA067529)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant P30-ES02109)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant R01-A1052267)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grantR01-CA108854)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/mi.2010.61en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleHelicobacter hepaticus infection in mice: models for understanding lower bowel inflammation and canceren_US
dc.typeArticleen_US
dc.identifier.citationFox, J G, Z Ge, M T Whary, S E Erdman, and B H Horwitz. “Helicobacter Hepaticus Infection in Mice: Models for Understanding Lower Bowel Inflammation and Cancer.” Mucosal Immunology 4, no. 1 (January 2011): 22–30.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicineen_US
dc.contributor.mitauthorFox, James G.en_US
dc.contributor.mitauthorGe, Zhongmingen_US
dc.contributor.mitauthorWhary, Mark T.en_US
dc.contributor.mitauthorErdman, Susan E.en_US
dc.relation.journalMucosal Immunologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsFox, J G; Ge, Z; Whary, M T; Erdman, S E; Horwitz, B Hen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9307-6116
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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