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Resumen
Foot-and-mouth disease (FMD) vaccines with improved stability and less reliant on a cold-chain are needed to improve the longevity of immune responses elicited in animals. This is especially so for serotypes O and SAT2 which are unstable in mildly acidic pH conditions or at elevated temperatures leading to dissociation of the capsid (146S particle) and loss of immunogenicity. Previously, stabilised SAT2 viruses were generated by reverse genetic approaches [ver mas...]
dc.contributor.authorScott, Katherine A.
dc.contributor.authorRathogwa, N.M.
dc.contributor.authorCapozzo, Alejandra
dc.contributor.authorMaree, Francois F.
dc.date.accessioned2018-03-09T16:33:26Z
dc.date.available2018-03-09T16:33:26Z
dc.date.issued2017
dc.identifier.issn0264-410X
dc.identifier.otherhttps://doi.org/10.1016/j.vaccine.2017.02.003
dc.identifier.urihttp://hdl.handle.net/20.500.12123/2007
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0264410X17301664?via%3Dihub
dc.description.abstractFoot-and-mouth disease (FMD) vaccines with improved stability and less reliant on a cold-chain are needed to improve the longevity of immune responses elicited in animals. This is especially so for serotypes O and SAT2 which are unstable in mildly acidic pH conditions or at elevated temperatures leading to dissociation of the capsid (146S particle) and loss of immunogenicity. Previously, stabilised SAT2 viruses were generated by reverse genetic approaches and assessed in vitro and in vivo with a guinea pig trial. Here we investigated the efficacy and comparative immunological responses of two thermostable and wild-type SAT2 vaccines over 5 months followed by challenge. We assessed humoral immune responses elicited in cattle in terms of total and neutralizing antibodies and IgG1/2 isotyping; and cell-mediated responses of IFN-γ as in vitro markers of protection. Whilst there were significant differences in total and neutralizing antibodies for the vSAT2-93H group compared to other vaccinated groups after the first vaccination, there were no significant differences after the second immunization. Following intra-dermolingual challenge all vaccinated groups were fully protected as determined by the absence of generalized lesions. These results provide proof that two vaccine doses, consisting of SAT2 antigen combined with ISA206B adjuvant, administered 4–6 weeks apart were able to protect animals up to 5 months pv. Additionally, vSAT2-93Y had significantly higher levels of IFN-γ after challenge and had a lower clinical score indicative of better protection compared to other vaccinated groups and the importance of cell mediated responses and antigen stability in protection.eng
dc.formatapplication/pdf
dc.language.isoeng
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.sourceVaccine 35 (40) : 5426-5433. (September 2017)
dc.subjectGanado Bovino
dc.subjectCattleeng
dc.subjectEnfermedades de los Animales
dc.subjectAnimal Diseaseseng
dc.subjectVirus de los Animales
dc.subjectAnimal Viruseseng
dc.subjectFiebre Aftosa
dc.subjectFoot and Mouth Diseaseeng
dc.titleEvaluation of immune responses of stabilised SAT2 antigens of foot-and-mouth disease in cattle
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.description.origenInst.de Virología
dc.gic155682
dc.description.filFil: Scott, Katherine A. Agricultural Research Council. Onderstepoort Veterinary Institute. Transboundary Animal Diseases Programme; Sudáfrica. University of Pretoria. Faculty of Veterinary Science. Department of Veterinary Tropical Diseases; Sudáfrica
dc.description.filFil: Rathogwa, N.M. Agricultural Research Council. Onderstepoort Veterinary Institute. Transboundary Animal Diseases Programme; Sudáfrica. University of Pretoria. Faculty of Agricultural and Natural Sciences. Department of Microbiology and Plant Pathology; Sudáfrica
dc.description.filFil: Capozzo, Alejandra. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología; Argentina
dc.description.filFil: Maree, Francois F. Agricultural Research Council. Onderstepoort Veterinary Institute. Transboundary Animal Diseases Programme; Sudáfrica. University of Pretoria. Faculty of Agricultural and Natural Sciences. Department of Microbiology and Plant Pathology; Sudáfrica
dc.subtypecientifico


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