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Campo DC | Valor | Lengua/Idioma |
---|---|---|
dc.contributor.author | Pino Tamayo, Paula Andrea | - |
dc.contributor.author | Puerta Arias, Juan David | - |
dc.contributor.author | Lopera Henao, Damaris Elena | - |
dc.contributor.author | Urán Jiménez, Martha Eugenia | - |
dc.contributor.author | González Marín, Ángel Augusto | - |
dc.date.accessioned | 2021-11-15T01:39:29Z | - |
dc.date.available | 2021-11-15T01:39:29Z | - |
dc.date.issued | 2016 | - |
dc.identifier.issn | 0962-9351 | - |
dc.identifier.uri | http://hdl.handle.net/10495/24116 | - |
dc.description.abstract | ABSTRACT: 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.extent | 18 | spa |
dc.format.mimetype | application/pdf | spa |
dc.language.iso | eng | spa |
dc.publisher | Hindawi | spa |
dc.type.hasversion | info:eu-repo/semantics/publishedVersion | spa |
dc.rights | info:eu-repo/semantics/openAccess | spa |
dc.rights.uri | http://creativecommons.org/licenses/by/2.5/co/ | * |
dc.title | Depletion of Neutrophils Exacerbates the Early Inflammatory Immune Response in Lungs of Mice Infected with Paracoccidioides brasiliensis | spa |
dc.type | info:eu-repo/semantics/article | spa |
dc.publisher.group | Grupo de Investigación en Microbiología Básica y Aplicada-Microba | spa |
dc.publisher.group | Micología Médica y Experimental | spa |
dc.identifier.doi | 10.1155/2016/3183285 | - |
oaire.version | http://purl.org/coar/version/c_970fb48d4fbd8a85 | spa |
dc.rights.accessrights | http://purl.org/coar/access_right/c_abf2 | spa |
dc.identifier.eissn | 1466-1861 | - |
oaire.citationtitle | Mediators of Inflammation | spa |
oaire.citationstartpage | 1 | spa |
oaire.citationendpage | 18 | spa |
oaire.citationvolume | 2016 | spa |
dc.rights.creativecommons | https://creativecommons.org/licenses/by/4.0/ | spa |
dc.publisher.place | Oxford, Estados Unidos | spa |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | spa |
dc.type.redcol | https://purl.org/redcol/resource_type/ART | spa |
dc.type.local | Artículo de investigación | spa |
dc.subject.decs | Paracoccidioides | - |
dc.subject.decs | Neutrófilos | - |
dc.subject.decs | Neutrophils | - |
dc.subject.decs | Ratones Endogámicos BALB C | - |
dc.subject.decs | Mice, Inbred BALB C | - |
dc.subject.decs | Paracoccidioidomicosis | - |
dc.subject.agrovoc | Paracoccidioidomycosis | - |
dc.description.researchgroupid | COL0126131 | spa |
dc.description.researchgroupid | COL0013709 | spa |
dc.relation.ispartofjournalabbrev | Mediators. Inflamm. | spa |
Aparece en las colecciones: | Artículos de Revista en Microbiología |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
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PuertaJuan_2016_DepletionInmune.pdf | Artículo de investigación | 7.17 MB | Adobe PDF | Visualizar/Abrir |
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