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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/74285
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dc.contributor.authorNegrini, Thais de C.-
dc.contributor.authorFerreira, Lucas S.-
dc.contributor.authorAlegranci, Pâmela-
dc.contributor.authorArthur, Rodrigo A.-
dc.contributor.authorSundfeld, Pedro P.-
dc.contributor.authorMaia, Danielle C. G.-
dc.contributor.authorSpolidório, Luis Carlos-
dc.contributor.authorCarlos, Iracilda Z.-
dc.date.accessioned2014-05-27T11:27:32Z-
dc.date.accessioned2016-10-25T18:41:38Z-
dc.date.available2014-05-27T11:27:32Z-
dc.date.available2016-10-25T18:41:38Z-
dc.date.issued2013-01-01-
dc.identifierhttp://dx.doi.org/10.3109/08820139.2012.719982-
dc.identifier.citationImmunological Investigations, v. 42, n. 1, p. 36-48, 2013.-
dc.identifier.issn0882-0139-
dc.identifier.issn1532-4311-
dc.identifier.urihttp://hdl.handle.net/11449/74285-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/74285-
dc.description.abstractSporotrichosis is an infection caused by the dimorphic fungus Sporothrix schenckii. Toll-like receptors (TLRs) play an important role in immunity, since they bind to pathogen surface antigens and initiate the immune response. However, little is known about the role of TLR-2 and fungal surface antigens in the recognition of S. schenckii and in the subsequent immune response. This study aimed to evaluate the involvement of TLR-2 and fungal surface soluble (SolAg) and lipidic (LipAg) antigens in phagocytosis of S. schenckii and production of immune mediators by macrophages obtained from WT and TLR-2 -/- animals. The results showed that TLR-2-/- animals had had statistical lower percentage of macrophages with internalized yeasts compared to WT. SolAg and LipAg impaired phagocytosis and immunological mediator production for both WT and TLR-2-/-. The absence of TLR-2 led to lower production of the cytokines TNF, IL-1β, IL-12 and IL-10 compared to WT animals. These results suggest a new insight in relation to how the immune system, through TLR-2, recognizes and induces the production of mediators in response to the fungus S. schenckii. Copyright © Informa Healthcare USA, Inc.en
dc.format.extent36-48-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectCytokines-
dc.subjectMacrophages-
dc.subjectMice-
dc.subjectPhagocytosis-
dc.subjectSporothrix schenckii-
dc.subjectTLR-2-
dc.subjectfungal lipidic antigen-
dc.subjectfungal surface soluble antigen-
dc.subjectfungus antigen-
dc.subjectinterleukin 10-
dc.subjectinterleukin 12-
dc.subjectinterleukin 1beta-
dc.subjecttoll like receptor 2-
dc.subjecttumor necrosis factor alpha-
dc.subjectunclassified drug-
dc.subjectanimal experiment-
dc.subjectcontrolled study-
dc.subjectcytokine production-
dc.subjectfemale-
dc.subjectinnate immunity-
dc.subjectmacrophage-
dc.subjectmouse-
dc.subjectnonhuman-
dc.subjectphagocytosis-
dc.subjectpriority journal-
dc.subjectAnimals-
dc.subjectAntigens, Fungal-
dc.subjectCells, Cultured-
dc.subjectFemale-
dc.subjectImmunity, Innate-
dc.subjectInflammation Mediators-
dc.subjectMice, Inbred C57BL-
dc.subjectMice, Knockout-
dc.subjectSporothrix-
dc.subjectSporotrichosis-
dc.subjectToll-Like Receptor 2-
dc.titleRole of TLR-2 and fungal surface antigens on innate immune response against Sporothrix schenckiien
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionSchool of Dentistry-
dc.contributor.institutionFederal University of Rio Grande do Sul-
dc.description.affiliationDepartment of Clinical Analysis Araraquara School of Pharmaceutical Sciences Sao Paulo State University, Rua Expedicionários do Brasil, No. 1621, Araraquara, SP, CEP 14.801-902-
dc.description.affiliationDepartment of Preventive and Community Dentistry Indiana University School of Dentistry, Indianapolis, IN-
dc.description.affiliationDepartment of Preventive and Community Dentistry School of Dentistry Federal University of Rio Grande do Sul, RS-
dc.description.affiliationDepartment of Physiology and Pathology Araraquara School of Dentistry São Paulo State University, SP-
dc.description.affiliationUnespDepartment of Clinical Analysis Araraquara School of Pharmaceutical Sciences Sao Paulo State University, Rua Expedicionários do Brasil, No. 1621, Araraquara, SP, CEP 14.801-902-
dc.description.affiliationUnespDepartment of Physiology and Pathology Araraquara School of Dentistry São Paulo State University, SP-
dc.identifier.doi10.3109/08820139.2012.719982-
dc.identifier.wosWOS:000312224700003-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofImmunological Investigations-
dc.identifier.scopus2-s2.0-84870950102-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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