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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/70928
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dc.contributor.authorAcorci, M. J.-
dc.contributor.authorDias-Melicio, L. A.-
dc.contributor.authorGolim, M. A.-
dc.contributor.authorBordon-Graciani, A. P.-
dc.contributor.authorPeraçoli, M. T S-
dc.contributor.authorSoares, A. M V C-
dc.date.accessioned2014-05-27T11:23:52Z-
dc.date.accessioned2016-10-25T18:26:51Z-
dc.date.available2014-05-27T11:23:52Z-
dc.date.available2016-10-25T18:26:51Z-
dc.date.issued2009-02-01-
dc.identifierhttp://dx.doi.org/10.1111/j.1365-3083.2008.02199.x-
dc.identifier.citationScandinavian Journal of Immunology, v. 69, n. 2, p. 73-79, 2009.-
dc.identifier.issn0300-9475-
dc.identifier.issn1365-3083-
dc.identifier.urihttp://hdl.handle.net/11449/70928-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/70928-
dc.description.abstractParacoccidioidomycosis (PCM) is a systemic mycosis caused by Paracoccidiodes brasiliensis that presents a wide spectrum of clinical manifestations. Because of the great number of neutrophils polymorphonuclear neutrophils (PMN) found in the P. brasiliensis granuloma, studies have been done to evaluate the role of these cells during the development of the infection. This fungus is found intracellularly in PMN and monocytes/macrophages, suggesting that it is capable of evading damage and surviving inside these cells. Thus, in the present study, we investigated whether P. brasiliensis can prolong the lifetime of PMN, and if this process would be related with IL-8 levels. PMN apoptosis and intracellular levels of IL-8 were analysed by flow cytometry and culture supernatants IL-8 levels were evaluated by enzyme-linked immunosorbent assay. We found that coincubation with P. brasiliensis yeast cells results in an inhibition of PMN apoptosis, which was associated with increase in IL-8 production by these cells. Cocultures treatment with monoclonal antibody anti-IL-8 reversed the inhibitory effect of P. brasiliensis on PMN apoptosis, besides to increase spontaneous apoptosis of these cells. These data show that, in contrast to other microbial pathogens that drive phagocytes into apoptosis to escape killing, P. brasiliensis can extend the lifetime of normal human PMN by inducing autocrine IL-8 production. © 2008 The Authors.en
dc.format.extent73-79-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectinterleukin 8-
dc.subjectinterleukin 8 antibody-
dc.subjectadult-
dc.subjectapoptosis-
dc.subjectcell culture-
dc.subjectcell level-
dc.subjectcell survival-
dc.subjectcontrolled study-
dc.subjectcytokine production-
dc.subjectcytokine release-
dc.subjectenzyme linked immunosorbent assay-
dc.subjectflow cytometry-
dc.subjecthuman-
dc.subjecthuman cell-
dc.subjectneutrophil-
dc.subjectnormal human-
dc.subjectParacoccidioides brasiliensis-
dc.subjectphagocyte-
dc.subjectpriority journal-
dc.subjectyeast cell-
dc.subjectAdult-
dc.subjectAntibodies, Monoclonal-
dc.subjectApoptosis-
dc.subjectHumans-
dc.subjectInterleukin-8-
dc.subjectMiddle Aged-
dc.subjectNeutrophils-
dc.subjectParacoccidioides-
dc.subjectPhagocytosis-
dc.titleInhibition of human neutrophil apoptosis by Paracoccidioides brasiliensis: Role of interleukin-8en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Microbiology and Immunology Biosciences Institute São Paulo State University, Botucatu, SP-
dc.description.affiliationBotucatu Blood Center School of Medicine São Paulo State University, Botucatu, SP-
dc.description.affiliationDepartment of Micro-biology and Immunology Biosciences Institute São Paulo State University, Botucatu, CEP 18618-000, SP-
dc.description.affiliationUnespDepartment of Microbiology and Immunology Biosciences Institute São Paulo State University, Botucatu, SP-
dc.description.affiliationUnespBotucatu Blood Center School of Medicine São Paulo State University, Botucatu, SP-
dc.description.affiliationUnespDepartment of Micro-biology and Immunology Biosciences Institute São Paulo State University, Botucatu, CEP 18618-000, SP-
dc.identifier.doi10.1111/j.1365-3083.2008.02199.x-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-58849133457.pdf-
dc.relation.ispartofScandinavian Journal of Immunology-
dc.identifier.scopus2-s2.0-58849133457-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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