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dc.contributor.authorPino Tamayo, Paula Andrea-
dc.contributor.authorPuerta Arias, Juan David-
dc.contributor.authorLopera Henao, Damaris Elena-
dc.contributor.authorUrán Jiménez, Martha Eugenia-
dc.contributor.authorGonzález Marín, Ángel Augusto-
dc.date.accessioned2021-11-15T01:39:29Z-
dc.date.available2021-11-15T01:39:29Z-
dc.date.issued2016-
dc.identifier.issn0962-9351-
dc.identifier.urihttp://hdl.handle.net/10495/24116-
dc.description.abstractABSTRACT: Neutrophils predominate during the acute phase of the Paracoccidioides brasiliensis infection. Herein, we determined the role of the neutrophil during the early stages of experimental pulmonary paracoccidioidomycosis using a monoclonal antibody (mAb) specific for neutrophils. Male BALB/c mice were inoculated intranasally with 1.5 × 106 or 2 × 106 P. brasiliensis yeast cells. The mAb was administered 24 h before infection, followed by doses every 48 h until mice were sacrificed. Survival time was evaluated and mice were sacrificed at 48 h and 96 h after inoculation to assess cellularity, fungal load, cytokine/chemokine levels, and histopathological analysis. Neutrophils from mAb-treated mice were efficiently depleted (99.04%). Eighty percent of the mice treated with the mAb and infected with 1.5 × 106 yeast cells died during the first two weeks after infection. When mice were treated and infected with 2 × 106 yeast cells, 100% of them succumbed by the first week after infection. During the acute inflammatory response significant increases in numbers of eosinophils, fungal load and levels of proinflammatory cytokines/chemokines were observed in the mAbtreated mice. We also confirmed that neutrophils are an important source of IFN-𝛾 and IL-17. These results indicate that neutrophils are essential for protection as well as being important for regulating the early inflammatory immune response in experimental pulmonary paracoccidioidomycosis.spa
dc.format.extent18spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherHindawispa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleDepletion of Neutrophils Exacerbates the Early Inflammatory Immune Response in Lungs of Mice Infected with Paracoccidioides brasiliensisspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGrupo de Investigación en Microbiología Básica y Aplicada-Microbaspa
dc.publisher.groupMicología Médica y Experimentalspa
dc.identifier.doi10.1155/2016/3183285-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1466-1861-
oaire.citationtitleMediators of Inflammationspa
oaire.citationstartpage1spa
oaire.citationendpage18spa
oaire.citationvolume2016spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
dc.publisher.placeOxford, Estados Unidosspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsParacoccidioides-
dc.subject.decsNeutrófilos-
dc.subject.decsNeutrophils-
dc.subject.decsRatones Endogámicos BALB C-
dc.subject.decsMice, Inbred BALB C-
dc.subject.decsParacoccidioidomicosis-
dc.subject.agrovocParacoccidioidomycosis-
dc.description.researchgroupidCOL0126131spa
dc.description.researchgroupidCOL0013709spa
dc.relation.ispartofjournalabbrevMediators. Inflamm.spa
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