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dc.contributor.authorZorzella-Pezavento, Sofia Fernanda Gonçalves-
dc.contributor.authorChiuso-Minicucci, Fernanda-
dc.contributor.authorFrança, Thais Graziela Donegá-
dc.contributor.authorIshikawa, Larissa Lumi Watanabe-
dc.contributor.authorDa Rosa, Larissa Camargo-
dc.contributor.authorMarques, Camila-
dc.contributor.authorIkoma, Maura Rosane Valerio-
dc.contributor.authorSartori, Alexandrina-
dc.date.accessioned2014-05-27T11:29:58Z-
dc.date.accessioned2016-10-25T18:51:17Z-
dc.date.available2014-05-27T11:29:58Z-
dc.date.available2016-10-25T18:51:17Z-
dc.date.issued2013-07-19-
dc.identifierhttp://dx.doi.org/10.1155/2013/519627-
dc.identifier.citationMediators of Inflammation, v. 2013.-
dc.identifier.issn0962-9351-
dc.identifier.issn1466-1861-
dc.identifier.urihttp://hdl.handle.net/11449/76011-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/76011-
dc.description.abstractExperimental autoimmune encephalomyelitis (EAE) is an artificially induced demyelination of the central nervous system (CNS) that resembles multiple sclerosis in its clinical, histopathological, and immunological features. Activated Th1 and Th17 cells are thought to be the main immunological players during EAE development. This study was designed to evaluate peripheral and local contribution of IL-17 to acute and chronic EAE stages. C57BL/6 mice were immunized with MOG plus complete Freund's adjuvant followed by pertussis toxin. Mice presented an initial acute phase characterized by accentuated weight loss and high clinical score, followed by a partial recovery when the animals reached normal body weight and smaller clinical scores. Spleen cells stimulated with MOG produced significantly higher levels of IFN-γ during the acute period whereas similar IL-17 levels were produced during both disease stages. CNS-infiltrating cells stimulated with MOG produced similar amounts of IFN-γ but, IL-17 was produced only at the acute phase of EAE. The percentage of Foxp3+ Treg cells, at the spleen and CNS, was elevated during both phases. The degree of inflammation was similar at both disease stages. Partial clinical recovery observed during chronic EAE was associated with no IL-17 production and presence of Foxp3+ Treg cells in the CNS. © 2013 Sofia Fernanda Gonçalves Zorzella-Pezavento et al.en
dc.language.isoeng-
dc.sourceScopus-
dc.subjectFreund adjuvant-
dc.subjectgamma interferon-
dc.subjectinterleukin 17-
dc.subjectmyelin oligodendrocyte glycoprotein-
dc.subjectpertussis toxin-
dc.subjecttranscription factor FOXP3-
dc.subjectallergic encephalomyelitis-
dc.subjectanimal cell-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectbody weight-
dc.subjectcell infiltration-
dc.subjectcontrolled study-
dc.subjectcytokine production-
dc.subjectdisease severity-
dc.subjectfemale-
dc.subjectinflammatory infiltrate-
dc.subjectmouse-
dc.subjectnervous system inflammation-
dc.subjectnonhuman-
dc.subjectpriority journal-
dc.subjectregulatory T lymphocyte-
dc.subjectscoring system-
dc.subjectspleen cell-
dc.subjectweight reduction-
dc.titlePersistent inflammation in the CNS during chronic EAE despite local absence of IL-17 productionen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionLaboratório de Citometria de Fluxo-Fundação-
dc.description.affiliationDepartment of Microbiology and Immunology Biosciences Institute Universidade Estadual Paulista (UNESP), 18618-070 Botucatu, SP-
dc.description.affiliationLaboratório de Citometria de Fluxo-Fundação, Dr. Amaral Carvalho, Jaú, SP-
dc.description.affiliationUnespDepartment of Microbiology and Immunology Biosciences Institute Universidade Estadual Paulista (UNESP), 18618-070 Botucatu, SP-
dc.identifier.doi10.1155/2013/519627-
dc.identifier.wosWOS:000321660200001-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-84880150391.pdf-
dc.relation.ispartofMediators of Inflammation-
dc.identifier.scopus2-s2.0-84880150391-
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