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Imbalance of IL-2, IFN-gamma and IL-10 secretion in the immunosuppression associated with human paracoccidioidomycosis

dc.contributor.authorBenard, G.
dc.contributor.authorRomano, C. C.
dc.contributor.authorCacere, C. R.
dc.contributor.authorJuvenale, M.
dc.contributor.authorMendes-Giannini, Maria José Soares [UNESP]
dc.contributor.authorDuarte, A. J. S.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:28:42Z
dc.date.available2014-05-20T15:28:42Z
dc.date.issued2001-02-21
dc.description.abstractPatients with paracoccidioidomycosis (PCM) display a certain degree of immunecompromise characterized by lymphocyte hyporesponsiveness to the main Paracoccidioides brasiliensis antigen (gp43). To determine whether cytokines are involved in this state, we evaluated the secretion of IL-2, IL-10 and IFN-gamma by peripheral blood mononuclear cells (PBMC) from patients with the acute (AF) and chronic (CF) forms of PCM and from healthy, P. brasiliensis-sensitized subjects. gp43-stimulated PBMC from healthy subjects produced substantial amounts of IL-2, IFN-gamma and IL-10, whereas PBMC from AF and CF patients produced low levels of IL-2 and IFN-gamma but substantial amounts of IL-10, Phytohaemagglutinin-induced cytokine secretion was comparable among AF and CF patients and healthy subjects, suggesting integrity of non-specific cellular immune mechanisms in PCM. gp43-pulsed adherent cells, but not non-adherent cells, mere the main source of IL-10, Moreover, IL-2 and IFN-gamma secretion correlated inversely with the amount of specific antibodies produced by patients and healthy subjects. Our results suggest that the imbalance in cytokine production of patients with PCM plays a role in the gp43-hyporesponsiveness and the marked (non-protective) antibody production of these patients. (C) 2001 Academic Press.en
dc.description.affiliationUSP, Fac Med, Lab Alergia & Imunol Clin & Expt, BR-01246903 São Paulo, Brazil
dc.description.affiliationUniv São Paulo, Fac Med, Hosp Clin, Clin Doencas Infecc & Parasitarias, São Paulo, Brazil
dc.description.affiliationUNESP, Fac Ciências Farmaceut, Dept Anal Clin, São Paulo, Brazil
dc.description.affiliationUnespUNESP, Fac Ciências Farmaceut, Dept Anal Clin, São Paulo, Brazil
dc.format.extent248-252
dc.identifierhttp://dx.doi.org/10.1006/cyto.2000.0824
dc.identifier.citationCytokine. Philadelphia: W B Saunders Co, v. 13, n. 4, p. 248-252, 2001.
dc.identifier.doi10.1006/cyto.2000.0824
dc.identifier.issn1043-4666
dc.identifier.orcid0000-0002-8059-0826
dc.identifier.urihttp://hdl.handle.net/11449/38455
dc.identifier.wosWOS:000167421500009
dc.language.isoeng
dc.publisherW B Saunders Co
dc.relation.ispartofCytokine
dc.relation.ispartofjcr3.514
dc.relation.ispartofsjr1,433
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectIL-2pt
dc.subjectIL-10pt
dc.subjectIFN-gammapt
dc.subjectparacoccidioidomycosispt
dc.subjectParacoccidioides brasiliensispt
dc.titleImbalance of IL-2, IFN-gamma and IL-10 secretion in the immunosuppression associated with human paracoccidioidomycosisen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderW B Saunders Co
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0002-8059-0826[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt

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