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Resumen
The purpose of this work was to characterize the cellular phenotype in inflammatory infiltrates of fetal tissues from pregnant heifers immunized and experimentally challenged with Neospora caninum. Fetuses from 20 heifers separated into 5 groups were obtained. The experiment was designed as follow: Group A, heifers inoculated intravenously with live tachyzoites of Argentine strain NC-6 (n = 4); Group B heifers inoculated subcutaneously with soluble native [ver mas...]
dc.contributor.authorRivera Maldonado, Juan E.
dc.contributor.authorDelay, Josepha
dc.contributor.authorHecker, Yanina
dc.contributor.authorMonterubbianesi, María Gloria
dc.contributor.authorCanton, German Jose
dc.contributor.authorCampero, Carlos Manuel
dc.contributor.authorOdeon, Anselmo Carlos
dc.contributor.authorMoore, Prando Dadin
dc.date.accessioned2019-10-29T14:32:23Z
dc.date.available2019-10-29T14:32:23Z
dc.date.issued2019-11
dc.identifier.issn0165-2427
dc.identifier.issn1873-2534
dc.identifier.otherhttps://doi.org/10.1016/j.vetimm.2019.109955
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S016524271930203X
dc.identifier.urihttp://hdl.handle.net/20.500.12123/6230
dc.description.abstractThe purpose of this work was to characterize the cellular phenotype in inflammatory infiltrates of fetal tissues from pregnant heifers immunized and experimentally challenged with Neospora caninum. Fetuses from 20 heifers separated into 5 groups were obtained. The experiment was designed as follow: Group A, heifers inoculated intravenously with live tachyzoites of Argentine strain NC-6 (n = 4); Group B heifers inoculated subcutaneously with soluble native antigen from the same strain formulated with immune stimulant complexes (ISCOMs) (n = 4); Group C heifers inoculated with recombinant proteins, rNcSAG1, rNcHSP20, rNcGRA7 formulated with ISCOMs (n = 4), Group D heifers inoculated subcutaneously with sterile phosphate buffered solution (n = 4) and Group E heifers inoculated subcutaneously with antigen-free ISCOMs (n = 4). Experimental challenge was performed at 70 days of gestation and all heifers were euthanized 34 days later. Fetal tissues were taken for histological studies. Inflammatory lesions were observed in brain and lung, and immunhistochemistry was used to identify CD3+, CD20+ and MHC II+ cells. The majority of the cells that infiltrate and circumscribe the lesions in the brain and lung tissue expressed MHC II antigen; varying between 70–90% of the total cellular infiltrate. CD3+ cells were also present within the lesions, contributing to up to 30% of the inflammatory cells. CD20+ cells appeared as a marginal group, in some cases, with a range between 10 and 25%. As expected, the immunolabeling of MHC II + and CD3 + cells in fetal tissues was associated with fetal infection with N. caninum. There were statistically significant differences in the distribution and population of the inflammatory infiltrate in relation to the immunogenic treatment and the type of tissue, with inflammatory cells being markedly less extensive fetuses from group A (dams previously exposed to N. caninum) and in brain tissue. This work showed that Neospora-infection induced MHC II+ and CD3+ cells in bovine fetuses from dams receiving experimental vaccineseng
dc.formatapplication/pdfes_AR
dc.language.isoenges_AR
dc.publisherElsevieres_AR
dc.rightsinfo:eu-repo/semantics/restrictedAccesses_AR
dc.sourceVeterinary Immunology and Immunopathology 217 : 109955 (November 2019)es_AR
dc.subjectNeospora Caninumes_AR
dc.subjectGanado Bovinoes_AR
dc.subjectCattleeng
dc.subjectFetoes_AR
dc.subjectFoetuseng
dc.subjectFenotiposes_AR
dc.subjectPhenotypeseng
dc.subjectEnfermedades de los Animales
dc.subjectAnimal Diseaseseng
dc.subject.otherNeosporosises_AR
dc.subject.otherBovinoses_AR
dc.titlePhenotypic characterization of immune cells in fetal tissues of cattle immunized and challenged with Neospora caninumes_AR
dc.typeinfo:ar-repo/semantics/artículoes_AR
dc.typeinfo:eu-repo/semantics/articlees_AR
dc.typeinfo:eu-repo/semantics/publishedVersiones_AR
dc.description.origenEEA Balcarcees_AR
dc.description.filFil: Maldonado Rivera, J.E. Universidad Nacional de Mar del Plata. Facultad de Ciencias Agrarias; Argentina. Universidad de Cuenca, Facultad de Ciencias Agropecuarias; Ecuador.es_AR
dc.description.filFil: DeLay, Josepha. University of Guelph. Animal Health Laboratory; Canadaes_AR
dc.description.filFil: Hecker, Yanina Paola. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Balcarce; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET); Argentina.es_AR
dc.description.filFil: Monterubbianesi, María Gloria. Universidad Nacional de Mar del Plata. Facultad de Ciencias Agrarias; Argentina.es_AR
dc.description.filFil: Cantón, Germán José. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Balcarce; Argentina.es_AR
dc.description.filFil: Campero, Carlos Manuel. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Balcarce; Argentina.es_AR
dc.description.filFil: Odeón, A.C. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Balcarce; Argentina.es_AR
dc.description.filFil: Moore, Dadin Prando. Universidad Nacional de Mar del Plata. Facultad de Ciencias Agrarias; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET); Argentina. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Balcarce; Argentina.es_AR
dc.subtypecientifico


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