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dc.contributor.authorZhou, Shenghua
dc.contributor.authorKurt-Jones, Evelyn A.
dc.contributor.authorFitzgerald, Katherine A.
dc.contributor.authorWang, Jennifer P.
dc.contributor.authorCerny, Anna M.
dc.contributor.authorChan, Melvin
dc.contributor.authorFinberg, Robert W.
dc.date2022-08-11T08:09:32.000
dc.date.accessioned2022-08-23T16:34:51Z
dc.date.available2022-08-23T16:34:51Z
dc.date.issued2007-04-04
dc.date.submitted2009-03-16
dc.identifier.citation<p>J Immunol. 2007 Apr 15;178(8):5173-81.</p>
dc.identifier.issn0022-1767 (Print)
dc.identifier.doi10.4049/jimmunol.178.8.5173
dc.identifier.pmid17404300
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38426
dc.description.abstractTLRs are important components of the innate immune response. The role of the TLR signaling pathway in host defense against a natural viral infection has been largely unexplored. We found that mice lacking MyD88, an essential adaptor protein in TLR signaling pathway, were extremely sensitive to intranasal infection with vesicular stomatitis virus, and this susceptibility was dose dependent. We demonstrated that this increased susceptibility correlates with the impaired production of IFN-alpha and defective induction and maintenance of neutralizing Ab. These studies outline the important role of the TLR signaling pathway in nasal mucosae-respiratory tracts-neuroepithelium environment in the protection against microbial pathogen infections. We believe that these results explain how the route of infection, probably by virtue of activating different cell populations, can lead to entirely different outcomes of infection based on the underlying genetics of the host.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=17404300&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.4049/jimmunol.178.8.5173
dc.subjectAnimals
dc.subjectAntibodies, Viral
dc.subjectCD4-Positive T-Lymphocytes
dc.subjectChemokine CCL2
dc.subjectDisease Susceptibility
dc.subjectInterferon Type II
dc.subjectInterferon-alpha
dc.subjectInterleukin-1
dc.subjectLymphocyte Activation
dc.subjectMice
dc.subjectMice, Inbred C57BL
dc.subjectMice, Knockout
dc.subjectMyeloid Differentiation Factor 88
dc.subjectRhabdoviridae Infections
dc.subject*Vesicular stomatitis Indiana virus
dc.subjectImmunology and Infectious Disease
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleRole of MyD88 in route-dependent susceptibility to vesicular stomatitis virus infection
dc.typeJournal Article
dc.source.journaltitleJournal of immunology (Baltimore, Md. : 1950)
dc.source.volume178
dc.source.issue8
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1293
dc.identifier.contextkey782962
html.description.abstract<p>TLRs are important components of the innate immune response. The role of the TLR signaling pathway in host defense against a natural viral infection has been largely unexplored. We found that mice lacking MyD88, an essential adaptor protein in TLR signaling pathway, were extremely sensitive to intranasal infection with vesicular stomatitis virus, and this susceptibility was dose dependent. We demonstrated that this increased susceptibility correlates with the impaired production of IFN-alpha and defective induction and maintenance of neutralizing Ab. These studies outline the important role of the TLR signaling pathway in nasal mucosae-respiratory tracts-neuroepithelium environment in the protection against microbial pathogen infections. We believe that these results explain how the route of infection, probably by virtue of activating different cell populations, can lead to entirely different outcomes of infection based on the underlying genetics of the host.</p>
dc.identifier.submissionpathoapubs/1293
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology
dc.source.pages5173-81


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