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Resumen
Fasciola hepatica, a worldwide distributed helminth, has a robust immunoregulatory effect in the host, increasing the susceptibility to secondary infections. Foot and mouth disease (FMD) is a highly contagious acute vesicular viral disease effectively controlled by vaccination in endemic regions. Despite the evidence of immunoregulatory effects, the impact of fasciolosis on the immune response induced by FMD vaccination in cattle has never been assessed. [ver mas...]
dc.contributor.authorCosta, Monique
dc.contributor.authorMansilla, Florencia Celeste
dc.contributor.authorSala, Juan Manuel
dc.contributor.authorSaravia, Anderson
dc.contributor.authorUbios, Diego
dc.contributor.authorLores, Pablo
dc.contributor.authorCapozzo, Alejandra
dc.contributor.authorFreire, Teresa
dc.date.accessioned2024-07-10T09:59:15Z
dc.date.available2024-07-10T09:59:15Z
dc.date.issued2024-01
dc.identifier.issn1873-2518
dc.identifier.otherhttps://doi.org/10.1016/j.vaccine.2023.12.067
dc.identifier.urihttp://hdl.handle.net/20.500.12123/18430
dc.identifier.urihttps://www.sciencedirect.com/science/article/abs/pii/S0264410X2301513X
dc.description.abstractFasciola hepatica, a worldwide distributed helminth, has a robust immunoregulatory effect in the host, increasing the susceptibility to secondary infections. Foot and mouth disease (FMD) is a highly contagious acute vesicular viral disease effectively controlled by vaccination in endemic regions. Despite the evidence of immunoregulatory effects, the impact of fasciolosis on the immune response induced by FMD vaccination in cattle has never been assessed. Our objective was to evaluate whether the infection by F. hepatica in cattle influences the long-term immunity elicited by the currently used commercial FMD-inactivated vaccines. Aberdeen Angus steers negative for F. hepatica were vaccinated twice against FMD virus (FMDV) during the first 6 months of age using a commercial oil vaccine formulated with A24/Cruzeiro and O1/Campos strains. When maternal antibodies against F. hepatica were weaned (18––20 months of age) animals were divided into groups of 12 and infected or mock-infected with 500 metacercariae/animal. Individual serum samples were collected at 0-, 28-, 59-, 87- and 157-days post-infection (dpi). Indirect ELISAs were used to detect A24/Cruzeiro specific bovine IgG and IgG subtypes. The total IgG antibody levels and avidity against FMDV did not show significant differences between all the groups. The commercial vaccine induced higher IgG2 than IgG1 titers in vaccinated animals. Anti-FMDV IgG1 levels significantly decreased in the infected group at 28 dpi. In addition, the avidity of IgG1 FMDV-specific antibodies at day 28 in the infected group was reduced compared to the control. These results show that F. hepatica infection modified anamnestic responses against FMDV, reducing serum IgG1 titers and avidity. To our knowledge, this is the first report of immune-regulation of F. hepatica altering the immune response of FMD vaccines, one of the most globally used animal vaccines.eng
dc.formatapplication/pdfes_AR
dc.language.isoenges_AR
dc.publisherElsevieres_AR
dc.rightsinfo:eu-repo/semantics/restrictedAccesses_AR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/es_AR
dc.sourceVaccine 42 (3) : 541-547 (January 2024)es_AR
dc.subjectFasciola hepaticaes_AR
dc.subjectFoot-and-mouth Diseaseeng
dc.subjectFiebre Aftosaes_AR
dc.subjectVaccineseng
dc.subjectVacunaes_AR
dc.subjectImmune Responseeng
dc.subjectRespuesta Inmunológicaes_AR
dc.subjectVacunación
dc.subjectVaccinationeng
dc.titleFasciola hepatica infection modifies IgG1 specific immune response to foot-and-mouth disease virus induced by vaccinationes_AR
dc.typeinfo:ar-repo/semantics/artículoes_AR
dc.typeinfo:eu-repo/semantics/articlees_AR
dc.typeinfo:eu-repo/semantics/publishedVersiones_AR
dc.rights.licenseCreative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)es_AR
dc.description.origenInstituto de Virologíaes_AR
dc.description.filFil: Costa, Monique. Universidad de La República. Facultad de Medicina. Departamento de Inmunobiología. Laboratorio de Inmunomodulación y Vacunas; Uruguayes_AR
dc.description.filFil: Mansilla, Florencia Celeste. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas; Argentinaes_AR
dc.description.filFil: Sala, Juan Manuel. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Mercedes; Argentinaes_AR
dc.description.filFil: Saravia, Anderson. Instituto Nacional de Investigación Agropecuaria. Plataforma de Investigación en Salud Animal; Uruguayes_AR
dc.description.filFil: Ubios, Diego. Instituto Nacional de Investigación Agropecuaria. Programa de Carne y Lana; Uruguayes_AR
dc.description.filFil: Lores, Pablo. Universidad de La República. Facultad de Medicina. Departamento de Inmunobiología. Laboratorio de Inmunomodulación y Vacunas; Uruguayes_AR
dc.description.filFil: Capozzo, Alejandra. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas; Argentinaes_AR
dc.description.filFil: Capozzo, Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes_AR
dc.description.filFil: Freire, Teresa. Universidad de La República. Facultad de Medicina. Departamento de Inmunobiología. Laboratorio de Inmunomodulación y Vacunas; Uruguayes_AR
dc.subtypecientifico


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