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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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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. |
format | Online Article Text |
id | pubmed-4348102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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