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Yersinia enterocolitica O : 3 isolated from patients with or without reactive arthritis induces polyclonal activation of B cells and autoantibody production in vivo

dc.contributor.authorSilva, EEC
dc.contributor.authorRamos, O. P.
dc.contributor.authorBauab, Taís Maria [UNESP]
dc.contributor.authorDeise Pasetto, F.
dc.contributor.authorde Medeiros, BMM
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:24:30Z
dc.date.available2014-05-20T13:24:30Z
dc.date.issued2003-07-01
dc.description.abstractThe mechanisms by which arthritis-provoking pathogens such as Yersinia enterocolitica interact with the human immune system to produce inflammatory synovitis are not well known. One of the immunomodulating mechanisms used against these pathogens is the polyclonal activation of lymphocytes. In this study, we investigated the extent of the B-lymphocyte activation induced in mice by a strain of Y. enterocolitica O:3 (FCF 526) isolated from a patient with arthritis, and compared it with two other strains, a virulent one (FCF 397[+]) isolated from a patient without arthritis and its plasmidless isogenic pair (FCF397[-]). Also we investigated the production of autoantibodies in mice infected with these different strains. SPF Swiss mice were infected intravenously with a suspension of Y. enterocolitica . Spleen cells were taken on days 7, 14, 21 and 28 after infection and the number of cells secreting nonspecific and specific antibodies of IgG 1 , IgG 2a , IgG 2b , IgG 3 , IgM and IgA isotypes were determined by the ELISPOT technique. The presence of autoantibodies in mouse serum was investigated by the dot-blot assay. The pattern of infection of the three bacterial strains were almost the same. We observed a general increase in the number of nonspecific Ig-secreting cells with all three strains, and the greatest increases observed were in the IgG 2a and IgG 3 isotypes. Only a small fraction of the immunoglobulins detected were antibacterial, suggesting that the rest resulted from polyclonal B cell activation. The strain isolated from the patient with arthritis (FCF526) induced the greatest production of autoantibodies, coinciding with the period in which the greatest activation of nonspecific B lymphocytes was seen. There were no signs of arthritis or inflammation in the joints of the infected animals. Based on our results, we were unable to determine whether there is an association between the arthritogenic capability of Y. enterocolitica and polyclonal activation of B cells.en
dc.description.affiliationUNESP, Fac Ciências Farmaceut, Dept Ciências Biol, Sch Pharmaceut Sci, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUnespUNESP, Fac Ciências Farmaceut, Dept Ciências Biol, Sch Pharmaceut Sci, BR-14801902 Araraquara, SP, Brazil
dc.format.extent261-268
dc.identifierhttp://dx.doi.org/10.1080/0891693031000151247
dc.identifier.citationAutoimmunity. Abingdon: Taylor & Francis Ltd, v. 36, n. 5, p. 261-268, 2003.
dc.identifier.doi10.1080/0891693031000151247
dc.identifier.issn0891-6934
dc.identifier.lattes4910754838277580
dc.identifier.urihttp://hdl.handle.net/11449/7615
dc.identifier.wosWOS:000184489800002
dc.language.isoeng
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofAutoimmunity
dc.relation.ispartofjcr2.648
dc.relation.ispartofsjr0,556
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectautoantibodiespt
dc.subjectpolyclonal B cell activationpt
dc.subjectreactive arthritispt
dc.titleYersinia enterocolitica O : 3 isolated from patients with or without reactive arthritis induces polyclonal activation of B cells and autoantibody production in vivoen
dc.typeArtigopt
dcterms.licensehttp://journalauthors.tandf.co.uk/permissions/reusingOwnWork.asp
dcterms.rightsHolderTaylor & Francis Ltd
dspace.entity.typePublication
relation.isDepartmentOfPublication5004bcab-94af-4939-b980-091ae9d0a19e
relation.isDepartmentOfPublication.latestForDiscovery5004bcab-94af-4939-b980-091ae9d0a19e
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes4910754838277580
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentCiências Biológicas - FCFpt

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