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Ag85A-specific CD4(+) T cell lines derived after boosting BCG-vaccinated cattle with Ad5-85A possess both mycobacterial growth inhibition and anti-inflammatory properties

There is a need to improve the efficacy of the BCG vaccine against human and bovine tuberculosis. Previous data showed that boosting bacilli Calmette-Guerin (BCG)-vaccinated cattle with a recombinant attenuated human type 5 adenovirally vectored subunit vaccine (Ad5-85A) increased BCG protection and...

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Autores principales: Metcalfe, Hannah J., Biffar, Lucia, Steinbach, Sabine, Guzman, Efrain, Connelley, Tim, Morrison, Ivan, Vordermeier, H. Martin, Villarreal-Ramos, Bernardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937909/
https://www.ncbi.nlm.nih.gov/pubmed/29655632
http://dx.doi.org/10.1016/j.vaccine.2018.03.068
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author Metcalfe, Hannah J.
Biffar, Lucia
Steinbach, Sabine
Guzman, Efrain
Connelley, Tim
Morrison, Ivan
Vordermeier, H. Martin
Villarreal-Ramos, Bernardo
author_facet Metcalfe, Hannah J.
Biffar, Lucia
Steinbach, Sabine
Guzman, Efrain
Connelley, Tim
Morrison, Ivan
Vordermeier, H. Martin
Villarreal-Ramos, Bernardo
author_sort Metcalfe, Hannah J.
collection PubMed
description There is a need to improve the efficacy of the BCG vaccine against human and bovine tuberculosis. Previous data showed that boosting bacilli Calmette-Guerin (BCG)-vaccinated cattle with a recombinant attenuated human type 5 adenovirally vectored subunit vaccine (Ad5-85A) increased BCG protection and was associated with increased frequency of Ag85A-specific CD4(+) T cells post-boosting. Here, the capacity of Ag85A-specific CD4(+) T cell lines – derived before and after viral boosting – to interact with BCG-infected macrophages was evaluated. No difference before and after boosting was found in the capacity of these Ag85A-specific CD4(+) T cell lines to restrict mycobacterial growth, but the secretion of IL-10 in vitro post-boost increased significantly. Furthermore, cell lines derived post-boost had no statistically significant difference in the secretion of pro-inflammatory cytokines (IL-1β, IL-12, IFNγ or TNFα) compared to pre-boost lines. In conclusion, the protection associated with the increased number of Ag85A-specific CD4(+) T cells restricting mycobacterial growth may be associated with anti-inflammatory properties to limit immune-pathology.
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spelling pubmed-59379092018-05-11 Ag85A-specific CD4(+) T cell lines derived after boosting BCG-vaccinated cattle with Ad5-85A possess both mycobacterial growth inhibition and anti-inflammatory properties Metcalfe, Hannah J. Biffar, Lucia Steinbach, Sabine Guzman, Efrain Connelley, Tim Morrison, Ivan Vordermeier, H. Martin Villarreal-Ramos, Bernardo Vaccine Article There is a need to improve the efficacy of the BCG vaccine against human and bovine tuberculosis. Previous data showed that boosting bacilli Calmette-Guerin (BCG)-vaccinated cattle with a recombinant attenuated human type 5 adenovirally vectored subunit vaccine (Ad5-85A) increased BCG protection and was associated with increased frequency of Ag85A-specific CD4(+) T cells post-boosting. Here, the capacity of Ag85A-specific CD4(+) T cell lines – derived before and after viral boosting – to interact with BCG-infected macrophages was evaluated. No difference before and after boosting was found in the capacity of these Ag85A-specific CD4(+) T cell lines to restrict mycobacterial growth, but the secretion of IL-10 in vitro post-boost increased significantly. Furthermore, cell lines derived post-boost had no statistically significant difference in the secretion of pro-inflammatory cytokines (IL-1β, IL-12, IFNγ or TNFα) compared to pre-boost lines. In conclusion, the protection associated with the increased number of Ag85A-specific CD4(+) T cells restricting mycobacterial growth may be associated with anti-inflammatory properties to limit immune-pathology. Elsevier Science 2018-05-11 /pmc/articles/PMC5937909/ /pubmed/29655632 http://dx.doi.org/10.1016/j.vaccine.2018.03.068 Text en © 2018 Department for Environment Food and Rural Affairs http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Metcalfe, Hannah J.
Biffar, Lucia
Steinbach, Sabine
Guzman, Efrain
Connelley, Tim
Morrison, Ivan
Vordermeier, H. Martin
Villarreal-Ramos, Bernardo
Ag85A-specific CD4(+) T cell lines derived after boosting BCG-vaccinated cattle with Ad5-85A possess both mycobacterial growth inhibition and anti-inflammatory properties
title Ag85A-specific CD4(+) T cell lines derived after boosting BCG-vaccinated cattle with Ad5-85A possess both mycobacterial growth inhibition and anti-inflammatory properties
title_full Ag85A-specific CD4(+) T cell lines derived after boosting BCG-vaccinated cattle with Ad5-85A possess both mycobacterial growth inhibition and anti-inflammatory properties
title_fullStr Ag85A-specific CD4(+) T cell lines derived after boosting BCG-vaccinated cattle with Ad5-85A possess both mycobacterial growth inhibition and anti-inflammatory properties
title_full_unstemmed Ag85A-specific CD4(+) T cell lines derived after boosting BCG-vaccinated cattle with Ad5-85A possess both mycobacterial growth inhibition and anti-inflammatory properties
title_short Ag85A-specific CD4(+) T cell lines derived after boosting BCG-vaccinated cattle with Ad5-85A possess both mycobacterial growth inhibition and anti-inflammatory properties
title_sort ag85a-specific cd4(+) t cell lines derived after boosting bcg-vaccinated cattle with ad5-85a possess both mycobacterial growth inhibition and anti-inflammatory properties
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937909/
https://www.ncbi.nlm.nih.gov/pubmed/29655632
http://dx.doi.org/10.1016/j.vaccine.2018.03.068
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