You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/8256
Full metadata record
DC FieldValueLanguage
dc.contributor.authorCamargo, Marcela Regina de-
dc.contributor.authorVenturini, James-
dc.contributor.authorVilani-Moreno, Fatima R.-
dc.contributor.authorArruda, Maria Sueli Parreira de-
dc.date.accessioned2014-05-20T13:25:54Z-
dc.date.available2014-05-20T13:25:54Z-
dc.date.issued2009-06-12-
dc.identifierhttp://dx.doi.org/10.1186/1471-2334-9-98-
dc.identifier.citationBmc Infectious Diseases. London: Biomed Central Ltd., v. 9, p. 8, 2009.-
dc.identifier.issn1471-2334-
dc.identifier.urihttp://hdl.handle.net/11449/8256-
dc.description.abstractBackground: In order to attain a better understanding of the interactions between opportunist fungi and their hosts, we investigated the cytokine profile associated with the inflammatory response to Candida albicans infection in mice with solid Ehrlich tumors of different degrees.Methods: Groups of eight animals were inoculated intraperitoneally with 5 x 10(6) C. albicans 7, 14 or 21 days after tumor implantation. After 24 or 72 hours, the animals were euthanized and intraperitoneal lavage fluid was collected. Peritoneal macrophages were cultivated and the levels of IFN-gamma, TNF-alpha, IL-12, IL-10 and IL-4 released into the supernatants were measured by ELISA. Kidney, liver and spleen samples were evaluated for fungal dissemination. Tumor-free animals and animals that had only been subjected to C. albicans infection were used as control groups.Results: Our results demonstrated that the mice produced more IFN-gamma and TNF-alpha and less IL-10, and also exhibited fungal clearance, at the beginning of tumor evolution. With the tumor progression, this picture changed: IL-10 production increased and IFN-gamma and TNF-alpha release decreased; furthermore, there was extensive fungal dissemination.Conclusion: Our results indicate that solid tumors can affect the production of macrophage cytokines and, in consequence, affect host resistance to opportunistic infections.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent8-
dc.language.isoeng-
dc.publisherBiomed Central Ltd.-
dc.sourceWeb of Science-
dc.titleModulation of macrophage cytokine profiles during solid tumor progression: susceptibility to Candida albicans infectionen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationSão Paulo State Univ, UNESP, Dept Biol Sci, Expt Immunol Lab,Coll Sci, BR-17047001 Bauru, SP, Brazil-
dc.description.affiliationSão Paulo State Univ, UNESP, Botucatu Med Sch, BR-18618970 Botucatu, SP, Brazil-
dc.description.affiliationInst Lauro Souza Lima, BR-17034971 Bauru, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, UNESP, Dept Biol Sci, Expt Immunol Lab,Coll Sci, BR-17047001 Bauru, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, UNESP, Botucatu Med Sch, BR-18618970 Botucatu, SP, Brazil-
dc.identifier.doi10.1186/1471-2334-9-98-
dc.identifier.wosWOS:000267750100001-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000267750100001.pdf-
dc.relation.ispartofBMC Infectious Diseases-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.