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Utilize este identificador para citar ou criar um link para este item: http://acervodigital.unesp.br/handle/11449/132267
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dc.contributor.authorRamos, Orivaldo Pereira-
dc.contributor.authorCangiani Silva, Eloisa Elena-
dc.contributor.authorFalcão, Deise Pasetto-
dc.contributor.authorMachado de Medeiros, Beatriz Maria-
dc.date.accessioned2014-05-27T11:21:17Z-
dc.date.accessioned2016-10-25T21:25:25Z-
dc.date.available2014-05-27T11:21:17Z-
dc.date.available2016-10-25T21:25:25Z-
dc.date.issued2005-03-29-
dc.identifierhttp://dx.doi.org/10.1111/j.1348-0421.2005.tb03712.x-
dc.identifier.citationMicrobiology and Immunology, v. 49, n. 2, p. 129-137, 2005.-
dc.identifier.issn0385-5600-
dc.identifier.urihttp://hdl.handle.net/11449/132267-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/132267-
dc.description.abstractPolyclonal lymphocyte stimulation is one of the immunomodulatory mechanisms induced by arthritogenic pathogens. In this study we examined the polyclonal activation potential of a virulent strain of Y. enterocolitica serotype O:8 (WA 2707+) and its plasmidless isogenic pair (WA 2707-). SPF Swiss mice were infected intragastrically and spleen cells were obtained on days 7, 14, 21, 28, 35 and 42 after infection. The number of cells secreting nonspecific immunoglobulins of IgG, IgM and IgA isotypes was determined by the ELISPOT technique. The presence of serum-specific antibodies was investigated by ELISA and the presence of autoantibodies by dot-blot assay. Although the patterns of infection of the two bacterial strains were almost the same, only the animals infected with the virulent strain presented clinical anomalies. Neither arthritic nor inflammatory signs were observed in the joints of the infected animals. The greatest activation observed was that of the nonspecific IgM-secreting cells, and their peak of secretion occurred between the 28th and the 42nd day after infection, for both strains of Y. enterocolitica O:8. Only the animals infected with the virulent strain (WA 2707+) produced IgG-specific antibodies in the serum, from the 28th day after infection. The serum of animals infected with either strain showed reactivity to all the autologous constituents tested, mainly on the 28th and 42nd day after infection. It was concluded that infection of mice with either the virulent strain of Y. enterocolitica O:8 or with its plasmidless isogenic pair resulted in the polyclonal activation of the splenic B lymphocytes including some autoreactive clones.en
dc.format.extent129-137-
dc.language.isoeng-
dc.publisherCenter Academic Publ Japan-
dc.sourceScopus-
dc.subjectAutoantibodies-
dc.subjectPolyclonal activation-
dc.subjectYersinia enterocolitica-
dc.subjectAutoantibody-
dc.subjectImmunoglobulin A antibody-
dc.subjectImmunoglobulin G antibody-
dc.subjectImmunoglobulin M antibody-
dc.subjectAnimal cell-
dc.subjectAnimal model-
dc.subjectAntibody blood level-
dc.subjectAntibody production-
dc.subjectAntibody specificity-
dc.subjectArthritis-
dc.subjectBacterial growth-
dc.subjectBacterial strain-
dc.subjectBacterial virulence-
dc.subjectCell count-
dc.subjectColony forming unit-
dc.subjectControlled study-
dc.subjectDot hybridization-
dc.subjectEnzyme linked immunosorbent assay-
dc.subjectEnzyme linked immunospot assay-
dc.subjectFemale-
dc.subjectImmunoglobulin production-
dc.subjectLymphocyte activation-
dc.subjectMouse-
dc.subjectNonhuman-
dc.subjectPolyclonal activation-
dc.subjectSpleen cell-
dc.subjectStrain difference-
dc.subjectAnimals-
dc.subjectAntibodies, Bacterial-
dc.subjectFemale-
dc.subjectImmunoglobulins-
dc.subjectLymphocyte Count-
dc.subjectLymphocytes-
dc.subjectMice-
dc.subjectSpleen-
dc.subjectTime Factors-
dc.subjectYersinia Infections-
dc.subjectAnimalia-
dc.subjectBacteria (microorganisms)-
dc.titleProduction of autoantibodies associated with polyclonal activation in Yersinia enterocolitica 0:8-infected miceen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Biological Sciences School of Pharmaceutical Sciences UNESP, Araraquara, SP-
dc.description.affiliationDepartamento de Ciencias Biologicas Faculdade de Ciencias Farmaceuticas UNESP, Rodovia Araraquara-Jaú, Km 1, 14801-902 Araraquara, SP-
dc.description.affiliationUnespDepartment of Biological Sciences School of Pharmaceutical Sciences UNESP, Araraquara, SP-
dc.description.affiliationUnespDepartamento de Ciencias Biologicas Faculdade de Ciencias Farmaceuticas UNESP, Rodovia Araraquara-Jaú, Km 1, 14801-902 Araraquara, SP-
dc.identifier.doi10.1111/j.1348-0421.2005.tb03712.x-
dc.identifier.wosWOS:000227142600005-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofMicrobiology and Immunology-
dc.identifier.scopus2-s2.0-14944363055-
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