dc.contributorUniv Fed Juiz de Fora
dc.contributorFed Univ Valleys Jequitinhonha & Mucuri
dc.contributorUniversidade Federal de São Paulo (UNIFESP)
dc.creatorDias, Alyria Teixeira
dc.creatorRibeiro De Castro, Sandra Bertelli
dc.creatorDe Souza Alves, Caio Cesar
dc.creatorMesquita, Felipe Pereira
dc.creatorVisona De Figueiredo, Nathalia Stela
dc.creatorEvangelista, Marcilene Gomes
dc.creatorMarques Nogueira Castanon, Maria Christina
dc.creatorJuliano, Maria Aparecida [UNIFESP]
dc.creatorFerreira, Ana Paula
dc.date.accessioned2016-01-24T14:39:58Z
dc.date.accessioned2022-10-07T20:47:03Z
dc.date.available2016-01-24T14:39:58Z
dc.date.available2022-10-07T20:47:03Z
dc.date.created2016-01-24T14:39:58Z
dc.date.issued2015-02-01
dc.identifierCellular Immunology. San Diego: Academic Press Inc Elsevier Science, v. 293, n. 2, p. 87-94, 2015.
dc.identifier0008-8749
dc.identifierhttp://repositorio.unifesp.br/handle/11600/38688
dc.identifier10.1016/j.cellimm.2014.12.009
dc.identifierWOS:000350089900005
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/4022804
dc.description.abstractMultiple sclerosis (MS) shows distinct clinical courses. Experimental autoimmune encephalomyelitis (EAE), a model to study multiple sclerosis, can be induced by different protocols, which show distinct cytokine and antibody production. the factors involved in this heterogeneity remain unclear. the relevance of MUG concentration in triggering a regulatory response in the chronic model of EAE is imprecise. the aim of this study was investigate if 100 or 300 mu g of MOG(35-55) could induce different EAE profiles. Modifications in the concentration of MUG were able to change the patterns of chemokines, cytokines, percentage of cells, inflammatory infiltrate and the development of a regulatory response. However, these changes were unable to modify the intensity of response, which explains the chronic progression of the disease in both concentrations. the results presented in this study contribute to understanding the intricate mechanisms that trigger EAE and provide insights into the pathogenesis of various forms of MS. (C) 2015 Elsevier Inc. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationCellular Immunology
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.rightsAcesso restrito
dc.subjectMultiple sclerosis
dc.subjectAnimal model
dc.subjectAutoimmunity
dc.subjectMOG(35-55)
dc.subjectCytokines
dc.titleDifferent MOG(35-55) concentrations induce distinguishable inflammation through early regulatory response by IL-10 and TGF-beta in mice CNS despite unchanged clinical course
dc.typeArtigo


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