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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/64864
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dc.contributor.authorMarques, M.-
dc.contributor.authorSoares, A.-
dc.contributor.authorFranco, M.-
dc.contributor.authorCamargo, Z. P.-
dc.contributor.authorMarques, S.-
dc.contributor.authorMemoes, R. P.-
dc.contributor.authorSouza, L. R.-
dc.contributor.authorCoelho, Kunie Iabuki Rabello-
dc.date.accessioned2014-05-27T11:18:07Z-
dc.date.accessioned2016-10-25T18:14:01Z-
dc.date.available2014-05-27T11:18:07Z-
dc.date.available2016-10-25T18:14:01Z-
dc.date.issued1996-10-19-
dc.identifierhttp://dx.doi.org/10.1080/02681219680000451-
dc.identifier.citationJournal of Medical and Veterinary Mycology, v. 34, n. 4, p. 265-272, 1996.-
dc.identifier.issn0268-1218-
dc.identifier.urihttp://hdl.handle.net/11449/64864-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/64864-
dc.description.abstractThe exoantigen of Paracoccidioides brasiliensis standardized by Camargo et al. [1] (AgR) was used to evaluate the in vivo and in vitro cell immune response of experimental animals and of patients with paracoccidioidomycosis (PBM). Fava Netto antigen (AgF) was tested in parallel as a control antigen. The study was conducted with mice and guinea pigs infected with P. brasiliensis or immunized with its fungal antigens, on patients with PBM and on their respective control groups. The cell immune response was analysed by skin tests, and by the macrophage and leucocyte migration inhibition tests (MMIT and LMIT) in the animals and in the patients, respectively. The skin test with AgR as paracoccidioidin was positive in infected or immunized mice and guinea pigs and negative in control animals. The skin tests with AgR (24 h) showed 96.7% positivity in patients with PBM and were negative in control individuals. Histopathological study of the in vivo tests in the different experimental models was consistent with a delayed hypersensitivity response (DHR). Immunohistochemical study of the skin tests of PBM patients demonstrated a predominance of T lymphocytes, confirming the nature of a DHR to the fungal antigens. The in vitro cell immune response showed variable results for the various experimental models, i.e. significant rates of MMIT in immunized mice, a tendency to positivity in infected guinea pigs, and the absence of migration inhibition in PBM patients. Taken together, the data indicate that the AgR is efficient as paracoccidioidin in the evaluation of DHR in PBM, with an optimum time of reading the test of 24 h.en
dc.format.extent265-272-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectParacoccidioides brasiliensis-
dc.subjectparacoccidioidin-
dc.subjectparacoccidioidomycosis-
dc.subjectfungus antigen-
dc.subjectallergenicity-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectantigen detection-
dc.subjectdelayed hypersensitivity-
dc.subjectguinea pig-
dc.subjectimmune response-
dc.subjectmacrophage migration-
dc.subjectmale-
dc.subjectmouse-
dc.subjectnonhuman-
dc.subjectparacoccidioides brasiliensis-
dc.subjectskin allergy-
dc.subjectskin test-
dc.subjectsouth american blastomycosis-
dc.subjectt lymphocyte activation-
dc.subjectAnimals-
dc.subjectAntigens, Fungal-
dc.subjectDermatitis, Allergic Contact-
dc.subjectGuinea Pigs-
dc.subjectHumans-
dc.subjectImmunity, Cellular-
dc.subjectLymphocytes-
dc.subjectMacrophages-
dc.subjectMale-
dc.subjectMice-
dc.subjectParacoccidioides-
dc.subjectParacoccidioidomycosis-
dc.subjectReference Values-
dc.subjectSkin-
dc.subjectSkin Tests-
dc.subjectAnimalia-
dc.subjectCavia-
dc.subjectCavia porcellus-
dc.subjectFava-
dc.subjectFungi-
dc.subjectparacoccidioidomycosis brasiliensis-
dc.subjectSus scrofa-
dc.titleEvaluation of Paracoccidioides brasiliensis exoantigen in the detection of delayed dermal hypersensitivity in experimental and human paracoccidioidomycosisen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionEscola Paulista de Medicina-
dc.description.affiliationDepartamento de Patologia Faculdade de Medicine de Botucotu Universidade Estadual Paulista 'Julio de Mesquita Filho' (UNESP), Botucotu, São Paulo-
dc.description.affiliationDivisão de Imunologia Institute de Biociências Universidade Estadual Paulista 'Julio de Mesquita Filho' (UNESP), Botucotu, São Paulo-
dc.description.affiliationDivisão de Biologia Celulor Escola Paulista de Medicina, São Paulo-
dc.description.affiliationDepartamento de Dermatologia Faculdade de Medidna de Botucotu Universidade Estadual Paulista 'Julio de Mesquita Filho' (UNESP), Botucotu, São Paulo-
dc.description.affiliationDepartamento de Moléstias Infecciosas Faculdade de Medicina de Botucotu Universidade Estadual Paulista 'Julio de Mesquita Filho' (UNESP), Botucotu, São Paulo-
dc.description.affiliationSchool of Medicine UNESP, Botucatu, Sao Paulo, CEP 18618-000-
dc.description.affiliationUnespDepartamento de Patologia Faculdade de Medicine de Botucotu Universidade Estadual Paulista 'Julio de Mesquita Filho' (UNESP), Botucotu, São Paulo-
dc.description.affiliationUnespDivisão de Imunologia Institute de Biociências Universidade Estadual Paulista 'Julio de Mesquita Filho' (UNESP), Botucotu, São Paulo-
dc.description.affiliationUnespDepartamento de Dermatologia Faculdade de Medidna de Botucotu Universidade Estadual Paulista 'Julio de Mesquita Filho' (UNESP), Botucotu, São Paulo-
dc.description.affiliationUnespDepartamento de Moléstias Infecciosas Faculdade de Medicina de Botucotu Universidade Estadual Paulista 'Julio de Mesquita Filho' (UNESP), Botucotu, São Paulo-
dc.description.affiliationUnespSchool of Medicine UNESP, Botucatu, Sao Paulo, CEP 18618-000-
dc.identifier.doi10.1080/02681219680000451-
dc.identifier.wosWOS:A1996VC30200006-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Medical and Veterinary Mycology-
dc.identifier.scopus2-s2.0-0029833646-
dc.identifier.scopus2-s2.0-79961136344-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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