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A Pool of Eight Virally Vectored African Swine Fever Antigens Protect Pigs against Fatal Disease

Classical approaches to African swine fever virus (ASFV) vaccine development have not been successful; inactivated virus does not provide protection and use of live attenuated viruses generated by passage in tissue culture had a poor safety profile. Current African swine fever (ASF) vaccine research...

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Autores principales: Goatley, Lynnette C., Reis, Ana Luisa, Portugal, Raquel, Goldswain, Hannah, Shimmon, Gareth L., Hargreaves, Zoe, Ho, Chak-Sum, Montoya, María, Sánchez-Cordón, Pedro J., Taylor, Geraldine, Dixon, Linda K., Netherton, Christopher L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349991/
https://www.ncbi.nlm.nih.gov/pubmed/32443536
http://dx.doi.org/10.3390/vaccines8020234
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author Goatley, Lynnette C.
Reis, Ana Luisa
Portugal, Raquel
Goldswain, Hannah
Shimmon, Gareth L.
Hargreaves, Zoe
Ho, Chak-Sum
Montoya, María
Sánchez-Cordón, Pedro J.
Taylor, Geraldine
Dixon, Linda K.
Netherton, Christopher L.
author_facet Goatley, Lynnette C.
Reis, Ana Luisa
Portugal, Raquel
Goldswain, Hannah
Shimmon, Gareth L.
Hargreaves, Zoe
Ho, Chak-Sum
Montoya, María
Sánchez-Cordón, Pedro J.
Taylor, Geraldine
Dixon, Linda K.
Netherton, Christopher L.
author_sort Goatley, Lynnette C.
collection PubMed
description Classical approaches to African swine fever virus (ASFV) vaccine development have not been successful; inactivated virus does not provide protection and use of live attenuated viruses generated by passage in tissue culture had a poor safety profile. Current African swine fever (ASF) vaccine research focuses on the development of modified live viruses by targeted gene deletion or subunit vaccines. The latter approach would be differentiation of vaccinated from infected animals (DIVA)-compliant, but information on which viral proteins to include in a subunit vaccine is lacking. Our previous work used DNA-prime/vaccinia-virus boost to screen 40 ASFV genes for immunogenicity, however this immunization regime did not protect animals after challenge. Here we describe the induction of both antigen and ASFV-specific antibody and cellular immune responses by different viral-vectored pools of antigens selected based on their immunogenicity in pigs. Immunization with one of these pools, comprising eight viral-vectored ASFV genes, protected 100% of pigs from fatal disease after challenge with a normally lethal dose of virulent ASFV. This data provide the basis for the further development of a subunit vaccine against this devastating disease.
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spelling pubmed-73499912020-07-22 A Pool of Eight Virally Vectored African Swine Fever Antigens Protect Pigs against Fatal Disease Goatley, Lynnette C. Reis, Ana Luisa Portugal, Raquel Goldswain, Hannah Shimmon, Gareth L. Hargreaves, Zoe Ho, Chak-Sum Montoya, María Sánchez-Cordón, Pedro J. Taylor, Geraldine Dixon, Linda K. Netherton, Christopher L. Vaccines (Basel) Article Classical approaches to African swine fever virus (ASFV) vaccine development have not been successful; inactivated virus does not provide protection and use of live attenuated viruses generated by passage in tissue culture had a poor safety profile. Current African swine fever (ASF) vaccine research focuses on the development of modified live viruses by targeted gene deletion or subunit vaccines. The latter approach would be differentiation of vaccinated from infected animals (DIVA)-compliant, but information on which viral proteins to include in a subunit vaccine is lacking. Our previous work used DNA-prime/vaccinia-virus boost to screen 40 ASFV genes for immunogenicity, however this immunization regime did not protect animals after challenge. Here we describe the induction of both antigen and ASFV-specific antibody and cellular immune responses by different viral-vectored pools of antigens selected based on their immunogenicity in pigs. Immunization with one of these pools, comprising eight viral-vectored ASFV genes, protected 100% of pigs from fatal disease after challenge with a normally lethal dose of virulent ASFV. This data provide the basis for the further development of a subunit vaccine against this devastating disease. MDPI 2020-05-18 /pmc/articles/PMC7349991/ /pubmed/32443536 http://dx.doi.org/10.3390/vaccines8020234 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Goatley, Lynnette C.
Reis, Ana Luisa
Portugal, Raquel
Goldswain, Hannah
Shimmon, Gareth L.
Hargreaves, Zoe
Ho, Chak-Sum
Montoya, María
Sánchez-Cordón, Pedro J.
Taylor, Geraldine
Dixon, Linda K.
Netherton, Christopher L.
A Pool of Eight Virally Vectored African Swine Fever Antigens Protect Pigs against Fatal Disease
title A Pool of Eight Virally Vectored African Swine Fever Antigens Protect Pigs against Fatal Disease
title_full A Pool of Eight Virally Vectored African Swine Fever Antigens Protect Pigs against Fatal Disease
title_fullStr A Pool of Eight Virally Vectored African Swine Fever Antigens Protect Pigs against Fatal Disease
title_full_unstemmed A Pool of Eight Virally Vectored African Swine Fever Antigens Protect Pigs against Fatal Disease
title_short A Pool of Eight Virally Vectored African Swine Fever Antigens Protect Pigs against Fatal Disease
title_sort pool of eight virally vectored african swine fever antigens protect pigs against fatal disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349991/
https://www.ncbi.nlm.nih.gov/pubmed/32443536
http://dx.doi.org/10.3390/vaccines8020234
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