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High Doses of Inactivated African Swine Fever Virus Are Safe, but Do Not Confer Protection against a Virulent Challenge

African swine fever (ASF) is currently the major concern of the global swine industry, as a consequence of which a reconsideration of the containment and prevention measures taken to date is urgently required. A great interest in developing an effective and safe vaccine against ASF virus (ASFV) infe...

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Autores principales: Cadenas-Fernández, Estefanía, Sánchez-Vizcaíno, Jose M., van den Born, Erwin, Kosowska, Aleksandra, van Kilsdonk, Emma, Fernández-Pacheco, Paloma, Gallardo, Carmina, Arias, Marisa, Barasona, Jose A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999564/
https://www.ncbi.nlm.nih.gov/pubmed/33802021
http://dx.doi.org/10.3390/vaccines9030242
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author Cadenas-Fernández, Estefanía
Sánchez-Vizcaíno, Jose M.
van den Born, Erwin
Kosowska, Aleksandra
van Kilsdonk, Emma
Fernández-Pacheco, Paloma
Gallardo, Carmina
Arias, Marisa
Barasona, Jose A.
author_facet Cadenas-Fernández, Estefanía
Sánchez-Vizcaíno, Jose M.
van den Born, Erwin
Kosowska, Aleksandra
van Kilsdonk, Emma
Fernández-Pacheco, Paloma
Gallardo, Carmina
Arias, Marisa
Barasona, Jose A.
author_sort Cadenas-Fernández, Estefanía
collection PubMed
description African swine fever (ASF) is currently the major concern of the global swine industry, as a consequence of which a reconsideration of the containment and prevention measures taken to date is urgently required. A great interest in developing an effective and safe vaccine against ASF virus (ASFV) infection has, therefore, recently appeared. The objective of the present study is to test an inactivated ASFV preparation under a vaccination strategy that has not previously been tested in order to improve its protective effect. The following have been considered: (i) virus inactivation by using a low binary ethyleneimine (BEI) concentration at a low temperature, (ii) the use of new and strong adjuvants; (iii) the use of very high doses (6 × 10(9) haemadsorption in 50% of infected cultures (HAD(50))), and (iv) simultaneous double inoculation by two different routes of administration: intradermal and intramuscular. Five groups of pigs were, therefore, inoculated with BEI- Pol16/DP/OUT21 in different adjuvant formulations, twice with a 4-week interval. Six weeks later, all groups were intramuscularly challenged with 10 HAD(50) of the virulent Pol16/DP/OUT21 ASFV isolate. All the animals had clinical signs and pathological findings consistent with ASF. This lack of effectiveness supports the claim that an inactivated virus strategy may not be a viable vaccine option with which to fight ASF.
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spelling pubmed-79995642021-03-28 High Doses of Inactivated African Swine Fever Virus Are Safe, but Do Not Confer Protection against a Virulent Challenge Cadenas-Fernández, Estefanía Sánchez-Vizcaíno, Jose M. van den Born, Erwin Kosowska, Aleksandra van Kilsdonk, Emma Fernández-Pacheco, Paloma Gallardo, Carmina Arias, Marisa Barasona, Jose A. Vaccines (Basel) Article African swine fever (ASF) is currently the major concern of the global swine industry, as a consequence of which a reconsideration of the containment and prevention measures taken to date is urgently required. A great interest in developing an effective and safe vaccine against ASF virus (ASFV) infection has, therefore, recently appeared. The objective of the present study is to test an inactivated ASFV preparation under a vaccination strategy that has not previously been tested in order to improve its protective effect. The following have been considered: (i) virus inactivation by using a low binary ethyleneimine (BEI) concentration at a low temperature, (ii) the use of new and strong adjuvants; (iii) the use of very high doses (6 × 10(9) haemadsorption in 50% of infected cultures (HAD(50))), and (iv) simultaneous double inoculation by two different routes of administration: intradermal and intramuscular. Five groups of pigs were, therefore, inoculated with BEI- Pol16/DP/OUT21 in different adjuvant formulations, twice with a 4-week interval. Six weeks later, all groups were intramuscularly challenged with 10 HAD(50) of the virulent Pol16/DP/OUT21 ASFV isolate. All the animals had clinical signs and pathological findings consistent with ASF. This lack of effectiveness supports the claim that an inactivated virus strategy may not be a viable vaccine option with which to fight ASF. MDPI 2021-03-10 /pmc/articles/PMC7999564/ /pubmed/33802021 http://dx.doi.org/10.3390/vaccines9030242 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Cadenas-Fernández, Estefanía
Sánchez-Vizcaíno, Jose M.
van den Born, Erwin
Kosowska, Aleksandra
van Kilsdonk, Emma
Fernández-Pacheco, Paloma
Gallardo, Carmina
Arias, Marisa
Barasona, Jose A.
High Doses of Inactivated African Swine Fever Virus Are Safe, but Do Not Confer Protection against a Virulent Challenge
title High Doses of Inactivated African Swine Fever Virus Are Safe, but Do Not Confer Protection against a Virulent Challenge
title_full High Doses of Inactivated African Swine Fever Virus Are Safe, but Do Not Confer Protection against a Virulent Challenge
title_fullStr High Doses of Inactivated African Swine Fever Virus Are Safe, but Do Not Confer Protection against a Virulent Challenge
title_full_unstemmed High Doses of Inactivated African Swine Fever Virus Are Safe, but Do Not Confer Protection against a Virulent Challenge
title_short High Doses of Inactivated African Swine Fever Virus Are Safe, but Do Not Confer Protection against a Virulent Challenge
title_sort high doses of inactivated african swine fever virus are safe, but do not confer protection against a virulent challenge
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999564/
https://www.ncbi.nlm.nih.gov/pubmed/33802021
http://dx.doi.org/10.3390/vaccines9030242
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