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Evaluation of macrophage activity and antibody production in genetically selected mice infected with Leptospira serovar pomona

dc.contributor.authorHaanwinckel, M. C. S. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:30:28Z
dc.date.available2014-05-20T15:30:28Z
dc.date.issued2008-01-01
dc.description.abstractThe aim of the present study was to evaluate the role of macrophage activity and antibody production in experimental infection with Leptospira Pomona in mice genetically selected for high (H) or low (L) humoral immune response. To evaluate macrophage activity, reactive oxygen and nitrogen intermediates were determined. Also, the production of tumor necrosis factor (TNF-alpha) and the recovery of Leptospira-specific antibodies in the kidneys and liver were assessed; histological lesions were analyzed using the hematoxylin-eosin technique, and Leptospira antigens in tissues were determined by immunohistochemistry. Results showed that recovery of microorganisms from the analyzed organs was lower in LIV-A mice. However, HIV-A animals showed total restraint since the 14th day after infection, whereas LIV-A mice still had bacteria in the liver at the 21st post-infection day. Immune response against Pomona serovar in those lineages was characterized as high production of antibodies, mainly in late periods of the infectious process. The production of reactive oxygen and nitrogen intermediates also contributed to the elimination of Leptospira Pomona in all two lineages; H2O2 production was an important factor in HIV-A mice, as well as NO production in the LIV-A animals, mainly at the latest post-inoculation periods. The same occurred regarding TNF-alpha production. Severe renal lesions were observed at periods in which larger numbers of leptospires were isolated using the culture technique. Tissue alterations persisted in LIV-A mice, even at periods in which leptospires were not recovered. Immunohistochemistry showed to be more sensitive than culturing. However, both techniques were appropriate for the agent identification in the studied lineages. Results suggest that such lineages could represent an important model to investigate pathogenesis and immune response against the varied serovars of leptospires.en
dc.description.affiliationUNESP, São Paulo State Univ, Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, São Paulo State Univ, Botucatu, SP, Brazil
dc.format.extent189-189
dc.identifierhttp://dx.doi.org/10.1590/S1678-91992008000100018
dc.identifier.citationJournal of Venomous Animals and Toxins Including Tropical Diseases. Botucatu: Cevap-unesp, v. 14, n. 1, p. 189-189, 2008.
dc.identifier.fileS1678-91992008000100018.pdf
dc.identifier.issn1678-9199
dc.identifier.scieloS1678-91992008000100018
dc.identifier.urihttp://hdl.handle.net/11449/39835
dc.identifier.wosWOS:000254511600018
dc.language.isoeng
dc.publisherUniversidade Estadual Paulista (Unesp), Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP)
dc.relation.ispartofJournal of Venomous Animals and Toxins Including Tropical Diseases
dc.relation.ispartofjcr1.782
dc.relation.ispartofsjr0,573
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectimmunological testsen
dc.subjectBiozzi miceen
dc.subjectexperimental infectionen
dc.subjectLeptospira interrogansen
dc.subjectserovar Pomonaen
dc.subjectmacrophagesen
dc.titleEvaluation of macrophage activity and antibody production in genetically selected mice infected with Leptospira serovar pomonaen
dc.typeArtigo
dcterms.licensehttp://www.scielo.br/revistas/jvatitd/iaboutj.htm
dcterms.rightsHolderCevap-unesp
dspace.entity.typePublication

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