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PCV2 vaccination induces IFN-γ/TNF-α co-producing T cells with a potential role in protection

Porcine circovirus type 2 (PCV2) is one of the economically most important pathogens for swine production worldwide. Vaccination is a powerful tool to control porcine circovirus diseases (PCVD). However, it is not fully understood how PCV2 vaccination interacts with the porcine immune system. Especi...

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Autores principales: Koinig, Hanna C, Talker, Stephanie C, Stadler, Maria, Ladinig, Andrea, Graage, Robert, Ritzmann, Mathias, Hennig-Pauka, Isabel, Gerner, Wilhelm, Saalmüller, Armin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348102/
https://www.ncbi.nlm.nih.gov/pubmed/25888899
http://dx.doi.org/10.1186/s13567-015-0157-4
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author Koinig, Hanna C
Talker, Stephanie C
Stadler, Maria
Ladinig, Andrea
Graage, Robert
Ritzmann, Mathias
Hennig-Pauka, Isabel
Gerner, Wilhelm
Saalmüller, Armin
author_facet Koinig, Hanna C
Talker, Stephanie C
Stadler, Maria
Ladinig, Andrea
Graage, Robert
Ritzmann, Mathias
Hennig-Pauka, Isabel
Gerner, Wilhelm
Saalmüller, Armin
author_sort Koinig, Hanna C
collection PubMed
description Porcine circovirus type 2 (PCV2) is one of the economically most important pathogens for swine production worldwide. Vaccination is a powerful tool to control porcine circovirus diseases (PCVD). However, it is not fully understood how PCV2 vaccination interacts with the porcine immune system. Especially knowledge on the cellular immune response against PCV2 is sparse. In this study we analysed antigen-specific T cell responses against PCV2 in a controlled vaccination and infection experiment. We focused on the ability of CD4(+) T cells to produce cytokines using multicolour flow cytometry (FCM). Vaccination with a PCV2 subunit vaccine (Ingelvac CircoFLEX®) induced PCV2-specific antibodies only in five out of 12 animals. Conversely, vaccine-antigen specific CD4(+) T cells which simultaneously produced IFN-γ and TNF-α and had a phenotype of central and effector memory T cells were detected in all vaccinated piglets. After challenge, seroconversion occurred earlier in vaccinated and infected pigs compared to the non-vaccinated, infected group. Vaccinated pigs were fully protected against viremia after subsequent challenge. Therefore, our data suggests that the induction of IFN-γ/TNF-α co-producing T cells by PCV2 vaccination may serve as a potential correlate of protection for this type of vaccine. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-015-0157-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-43481022015-03-05 PCV2 vaccination induces IFN-γ/TNF-α co-producing T cells with a potential role in protection Koinig, Hanna C Talker, Stephanie C Stadler, Maria Ladinig, Andrea Graage, Robert Ritzmann, Mathias Hennig-Pauka, Isabel Gerner, Wilhelm Saalmüller, Armin Vet Res Research Porcine circovirus type 2 (PCV2) is one of the economically most important pathogens for swine production worldwide. Vaccination is a powerful tool to control porcine circovirus diseases (PCVD). However, it is not fully understood how PCV2 vaccination interacts with the porcine immune system. Especially knowledge on the cellular immune response against PCV2 is sparse. In this study we analysed antigen-specific T cell responses against PCV2 in a controlled vaccination and infection experiment. We focused on the ability of CD4(+) T cells to produce cytokines using multicolour flow cytometry (FCM). Vaccination with a PCV2 subunit vaccine (Ingelvac CircoFLEX®) induced PCV2-specific antibodies only in five out of 12 animals. Conversely, vaccine-antigen specific CD4(+) T cells which simultaneously produced IFN-γ and TNF-α and had a phenotype of central and effector memory T cells were detected in all vaccinated piglets. After challenge, seroconversion occurred earlier in vaccinated and infected pigs compared to the non-vaccinated, infected group. Vaccinated pigs were fully protected against viremia after subsequent challenge. Therefore, our data suggests that the induction of IFN-γ/TNF-α co-producing T cells by PCV2 vaccination may serve as a potential correlate of protection for this type of vaccine. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-015-0157-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-03 2015 /pmc/articles/PMC4348102/ /pubmed/25888899 http://dx.doi.org/10.1186/s13567-015-0157-4 Text en © Koinig et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Koinig, Hanna C
Talker, Stephanie C
Stadler, Maria
Ladinig, Andrea
Graage, Robert
Ritzmann, Mathias
Hennig-Pauka, Isabel
Gerner, Wilhelm
Saalmüller, Armin
PCV2 vaccination induces IFN-γ/TNF-α co-producing T cells with a potential role in protection
title PCV2 vaccination induces IFN-γ/TNF-α co-producing T cells with a potential role in protection
title_full PCV2 vaccination induces IFN-γ/TNF-α co-producing T cells with a potential role in protection
title_fullStr PCV2 vaccination induces IFN-γ/TNF-α co-producing T cells with a potential role in protection
title_full_unstemmed PCV2 vaccination induces IFN-γ/TNF-α co-producing T cells with a potential role in protection
title_short PCV2 vaccination induces IFN-γ/TNF-α co-producing T cells with a potential role in protection
title_sort pcv2 vaccination induces ifn-γ/tnf-α co-producing t cells with a potential role in protection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348102/
https://www.ncbi.nlm.nih.gov/pubmed/25888899
http://dx.doi.org/10.1186/s13567-015-0157-4
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