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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7349991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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