Foot-and-mouth disease vaccination induces cross-reactive IFN-γ responses in cattle that are dependent on the integrity of the 140S particles

Interferon-γ (IFN-γ) recall responses against foot-and-mouth disease virus (FMDV) in FMD vaccinated cattle are utilized to study T-lymphocyte immunity against this virus. Here, a recall IFN-γ assay based on a commercial ELISA was set up using 308 samples from naïve and vaccinated cattle. The assay w...

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Detalhes bibliográficos
Autores: Bucafusco, Danilo, Di Giacomo, Sebastián, Pega, Juan Franco, Schammas, Juan Manuel, Cardoso, Nancy Patricia, Capozzo, Alejandra Victoria, Perez Filgueira, Daniel Mariano
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2015
País:Argentina
Recursos:Instituto Nacional de Tecnología Agropecuaria
Repositorio:INTA Digital (INTA)
Idioma:inglés
OAI Identifier:oai:localhost:20.500.12123/2516
Acesso em linha:https://www.sciencedirect.com/science/article/pii/S0042682214005315
http://hdl.handle.net/20.500.12123/2516
https://doi.org/10.1016/j.virol.2014.11.023
Access Level:acceso abierto
Palavra-chave:Ganado Bovino
Enfermedades de los Animales
Fiebre Aftosa
Vacunación
Interferonas
Cattle
Animal Diseases
Foot and Mouth Disease
Vaccination
Interferons
Descrição
Resumo:Interferon-γ (IFN-γ) recall responses against foot-and-mouth disease virus (FMDV) in FMD vaccinated cattle are utilized to study T-lymphocyte immunity against this virus. Here, a recall IFN-γ assay based on a commercial ELISA was set up using 308 samples from naïve and vaccinated cattle. The assay was used to study cross-reactive responses between different FMDV vaccine strains. Blood samples from cattle immunized with monovalent vaccines containing A24/Cruzeiro/Brazil/55, A/Argentina/2001 or O1/Campos/Brazil/58 strains were tested using purified-inactivated FMDV from homologous and heterologous strains. A24/Cruzeiro was the most efficient IFN-γ inducer in all vaccinated animals, both when included in the vaccine or as stimulating antigen. We demonstrate that this was mainly due to the structural stability of the whole viral particle. These results show that IFN-γ production relies on the presence of 140S particles that can maintain their integrity along the incubation process in vitro, and throughout the vaccine´s shelf-life, when used in vivo.