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dc.contributor.authorWang, Jennifer P.
dc.contributor.authorKurt-Jones, Evelyn A.
dc.contributor.authorShin, Ok S.
dc.contributor.authorManchak, Michael D.
dc.contributor.authorLevin, Myron J.
dc.contributor.authorFinberg, Robert W.
dc.date2022-08-11T08:09:34.000
dc.date.accessioned2022-08-23T16:35:52Z
dc.date.available2022-08-23T16:35:52Z
dc.date.issued2005-09-29
dc.date.submitted2009-03-26
dc.identifier.citationJ Virol. 2005 Oct;79(20):12658-66. <a href="http://dx.doi.org/10.1128/JVI.79.20.12658-12666.2005">Link to article on publisher's site</a>
dc.identifier.issn0022-538X (Print)
dc.identifier.doi10.1128/JVI.79.20.12658-12666.2005
dc.identifier.pmid16188968
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38658
dc.description.abstractThe pattern recognition receptor Toll-like receptor 2 (TLR2) has been implicated in the response to several human viruses, including herpes simplex viruses (types 1 and 2) and cytomegalovirus. We demonstrated that varicella-zoster virus (VZV) activates inflammatory cytokine responses via TLR2. VZV specifically induced interleukin-6 (IL-6) in human monocytes via TLR2-dependent activation of NF-kappaB, and small interfering RNA designed to suppress TLR2 mRNA reduced the IL-6 response to VZV in human monocyte-derived macrophages. Unlike other herpesviruses, the cytokine response to VZV was species specific. VZV did not induce cytokines in murine embryonic fibroblasts or in a mouse cell line, although VZV did activate NF-kappaB in a human cell line expressing a murine TLR2 construct. Together, these results suggest that TLR2 may play a role in the inflammatory response to VZV infection.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=16188968&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectAnimals
dc.subjectCells, Cultured
dc.subjectCytokines
dc.subjectEnzyme-Linked Immunosorbent Assay
dc.subjectFlow Cytometry
dc.subjectHerpes Zoster
dc.subjectHerpesvirus 3, Human
dc.subjectHumans
dc.subjectInflammation
dc.subjectInterleukin-6
dc.subjectMacrophages
dc.subjectMembrane Glycoproteins
dc.subjectMice
dc.subjectMonocytes
dc.subjectNF-kappa B
dc.subjectRNA, Small Interfering
dc.subjectReceptors, Cell Surface
dc.subjectSpecies Specificity
dc.subjectToll-Like Receptor 2
dc.subjectToll-Like Receptors
dc.subjectUp-Regulation
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleVaricella-zoster virus activates inflammatory cytokines in human monocytes and macrophages via Toll-like receptor 2
dc.typeJournal Article
dc.source.journaltitleJournal of virology
dc.source.volume79
dc.source.issue20
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2515&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1516
dc.identifier.contextkey798491
refterms.dateFOA2022-08-23T16:35:52Z
html.description.abstract<p>The pattern recognition receptor Toll-like receptor 2 (TLR2) has been implicated in the response to several human viruses, including herpes simplex viruses (types 1 and 2) and cytomegalovirus. We demonstrated that varicella-zoster virus (VZV) activates inflammatory cytokine responses via TLR2. VZV specifically induced interleukin-6 (IL-6) in human monocytes via TLR2-dependent activation of NF-kappaB, and small interfering RNA designed to suppress TLR2 mRNA reduced the IL-6 response to VZV in human monocyte-derived macrophages. Unlike other herpesviruses, the cytokine response to VZV was species specific. VZV did not induce cytokines in murine embryonic fibroblasts or in a mouse cell line, although VZV did activate NF-kappaB in a human cell line expressing a murine TLR2 construct. Together, these results suggest that TLR2 may play a role in the inflammatory response to VZV infection.</p>
dc.identifier.submissionpathoapubs/1516
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology
dc.source.pages12658-66


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