The FlagT4G Vaccine Confers a Strong and Regulated Immunity and Early Virological Protection against Classical Swine Fever

Control of classical swine fever virus (CSFV) in endemic countries relies on vaccination, mostly using vaccines that do not allow for differentiation of vaccinated from infected animals (DIVA). FlagT4G vaccine is a novel candidate that confers robust immunity and shows DIVA capabilities. The present...

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Detalhes bibliográficos
Autores: Bohórquez Garzón, José Alejandro|||0000-0002-6715-1757, Wang, Miaomiao, Díaz, Ivan|||0000-0002-8090-1073, Alberch, Mònica, Pérez-Simó, Marta, Rosell, Rosa|||0000-0002-8294-1159, Gladue, Douglas P.|||0000-0002-7894-0233, Borca, Manuel V., Ganges, Llilianne|||0000-0002-8644-3560
Tipo de documento: artigo
Data de publicação:2022
País:España
Recursos:Universitat Autònoma de Barcelona
Repositório:Dipòsit Digital de Documents de la UAB
Idioma:inglês
OAI Identifier:oai:ddd.uab.cat:266276
Acesso em linha:https://ddd.uab.cat/record/266276
https://dx.doi.org/urn:doi:10.3390/v14091954
Access Level:Acceso aberto
Palavra-chave:Vaccine efficacy
CSFV
Innate immunity
FlagT4G
Marker vaccine
Virological protection
Antibody response
Descrição
Resumo:Control of classical swine fever virus (CSFV) in endemic countries relies on vaccination, mostly using vaccines that do not allow for differentiation of vaccinated from infected animals (DIVA). FlagT4G vaccine is a novel candidate that confers robust immunity and shows DIVA capabilities. The present study assessed the immune response elicited by FlagT4G and its capacity to protect pigs for a short time after vaccination. Five days after a single dose of FlagT4G vaccine, animals were challenged with a highly virulent CSFV strain. A strong, but regulated, interferon-α response was found after vaccination. Vaccinated animals showed clinical and virological protection against the challenge, in the absence of antibody response at 5 days post-vaccination. Upon challenge, a rapid rise in the titers of CSFV neutralizing antibodies and an increase in the IFN-γ producing cells were noticed in all vaccinated-challenged pigs. Meanwhile, unvaccinated pigs showed severe clinical signs and high viral replication, being euthanized before the end of the trial. These animals were unable to generate neutralizing antibodies and IFN-γ responses after the CSFV challenge. The results from the present study assert the fast and efficient protection by FlagT4G, a highly promising tool for CSFV control worldwide.