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Cellular and Humoral Immune Responses after Immunisation with Low Virulent African Swine Fever Virus in the Large White Inbred Babraham Line and Outbred Domestic Pigs

African swine fever virus is currently present in all of the world’s continents apart from Antarctica, and efforts to control the disease are hampered by the lack of a commercially available vaccine. The Babraham large white pig is a highly inbred line that could represent a powerful tool to improve...

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Autores principales: Goatley, Lynnette C., Nash, Rachel H., Andrews, Catherine, Hargreaves, Zoe, Tng, Priscilla, Reis, Ana Luisa, Graham, Simon P., Netherton, Christopher L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322176/
https://www.ncbi.nlm.nih.gov/pubmed/35891467
http://dx.doi.org/10.3390/v14071487
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author Goatley, Lynnette C.
Nash, Rachel H.
Andrews, Catherine
Hargreaves, Zoe
Tng, Priscilla
Reis, Ana Luisa
Graham, Simon P.
Netherton, Christopher L.
author_facet Goatley, Lynnette C.
Nash, Rachel H.
Andrews, Catherine
Hargreaves, Zoe
Tng, Priscilla
Reis, Ana Luisa
Graham, Simon P.
Netherton, Christopher L.
author_sort Goatley, Lynnette C.
collection PubMed
description African swine fever virus is currently present in all of the world’s continents apart from Antarctica, and efforts to control the disease are hampered by the lack of a commercially available vaccine. The Babraham large white pig is a highly inbred line that could represent a powerful tool to improve our understanding of the protective immune responses to this complex pathogen; however, previous studies indicated differential vaccine responses after the African swine fever virus challenge of inbred minipigs with different swine leukocyte antigen haplotypes. Lymphocyte numbers and African swine fever virus-specific antibody and T-cell responses were measured in inbred and outbred animals after inoculation with a low virulent African swine fever virus isolate and subsequent challenge with a related virulent virus. Surprisingly, diminished immune responses were observed in the Babraham pigs when compared to the outbred animals, and the inbred pigs were not protected after challenge. Recovery of Babraham pigs after challenge weakly correlated with antibody responses, whereas protective responses in outbred animals more closely correlated with the T-cell response. The Babraham pig may, therefore, represent a useful model for studying the role of antibodies in protection against the African swine fever virus.
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spelling pubmed-93221762022-07-27 Cellular and Humoral Immune Responses after Immunisation with Low Virulent African Swine Fever Virus in the Large White Inbred Babraham Line and Outbred Domestic Pigs Goatley, Lynnette C. Nash, Rachel H. Andrews, Catherine Hargreaves, Zoe Tng, Priscilla Reis, Ana Luisa Graham, Simon P. Netherton, Christopher L. Viruses Article African swine fever virus is currently present in all of the world’s continents apart from Antarctica, and efforts to control the disease are hampered by the lack of a commercially available vaccine. The Babraham large white pig is a highly inbred line that could represent a powerful tool to improve our understanding of the protective immune responses to this complex pathogen; however, previous studies indicated differential vaccine responses after the African swine fever virus challenge of inbred minipigs with different swine leukocyte antigen haplotypes. Lymphocyte numbers and African swine fever virus-specific antibody and T-cell responses were measured in inbred and outbred animals after inoculation with a low virulent African swine fever virus isolate and subsequent challenge with a related virulent virus. Surprisingly, diminished immune responses were observed in the Babraham pigs when compared to the outbred animals, and the inbred pigs were not protected after challenge. Recovery of Babraham pigs after challenge weakly correlated with antibody responses, whereas protective responses in outbred animals more closely correlated with the T-cell response. The Babraham pig may, therefore, represent a useful model for studying the role of antibodies in protection against the African swine fever virus. MDPI 2022-07-07 /pmc/articles/PMC9322176/ /pubmed/35891467 http://dx.doi.org/10.3390/v14071487 Text en © 2022 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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Goatley, Lynnette C.
Nash, Rachel H.
Andrews, Catherine
Hargreaves, Zoe
Tng, Priscilla
Reis, Ana Luisa
Graham, Simon P.
Netherton, Christopher L.
Cellular and Humoral Immune Responses after Immunisation with Low Virulent African Swine Fever Virus in the Large White Inbred Babraham Line and Outbred Domestic Pigs
title Cellular and Humoral Immune Responses after Immunisation with Low Virulent African Swine Fever Virus in the Large White Inbred Babraham Line and Outbred Domestic Pigs
title_full Cellular and Humoral Immune Responses after Immunisation with Low Virulent African Swine Fever Virus in the Large White Inbred Babraham Line and Outbred Domestic Pigs
title_fullStr Cellular and Humoral Immune Responses after Immunisation with Low Virulent African Swine Fever Virus in the Large White Inbred Babraham Line and Outbred Domestic Pigs
title_full_unstemmed Cellular and Humoral Immune Responses after Immunisation with Low Virulent African Swine Fever Virus in the Large White Inbred Babraham Line and Outbred Domestic Pigs
title_short Cellular and Humoral Immune Responses after Immunisation with Low Virulent African Swine Fever Virus in the Large White Inbred Babraham Line and Outbred Domestic Pigs
title_sort cellular and humoral immune responses after immunisation with low virulent african swine fever virus in the large white inbred babraham line and outbred domestic pigs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322176/
https://www.ncbi.nlm.nih.gov/pubmed/35891467
http://dx.doi.org/10.3390/v14071487
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