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High-dose Mycobacterium tuberculosis aerosol challenge cannot overcome BCG-induced protection in Chinese origin cynomolgus macaques; implications of natural resistance for vaccine evaluation

This study describes the use of cynomolgus macaques of Chinese origin (CCM) to evaluate the efficacy and immunogenicity of the BCG vaccine against high dose aerosol Mycobacterium tuberculosis challenge. Progressive disease developed in three of the unvaccinated animals within 10 weeks of challenge,...

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Autores principales: Sibley, Laura, White, Andrew D., Gooch, Karen E., Stevens, Lisa M., Tanner, Rachel, Jacobs, Ashley, Daykin-Pont, Owen, Gleeson, Fergus, McIntyre, Anthony, Basaraba, Randall, Clark, Simon, Hall, Graham, Pearson, Geoff, Rayner, Emma, McShane, Helen, Williams, Ann, Dennis, Mike, Marsh, Philip D., Sharpe, Sally
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192909/
https://www.ncbi.nlm.nih.gov/pubmed/34112845
http://dx.doi.org/10.1038/s41598-021-90913-0
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author Sibley, Laura
White, Andrew D.
Gooch, Karen E.
Stevens, Lisa M.
Tanner, Rachel
Jacobs, Ashley
Daykin-Pont, Owen
Gleeson, Fergus
McIntyre, Anthony
Basaraba, Randall
Clark, Simon
Hall, Graham
Pearson, Geoff
Rayner, Emma
McShane, Helen
Williams, Ann
Dennis, Mike
Marsh, Philip D.
Sharpe, Sally
author_facet Sibley, Laura
White, Andrew D.
Gooch, Karen E.
Stevens, Lisa M.
Tanner, Rachel
Jacobs, Ashley
Daykin-Pont, Owen
Gleeson, Fergus
McIntyre, Anthony
Basaraba, Randall
Clark, Simon
Hall, Graham
Pearson, Geoff
Rayner, Emma
McShane, Helen
Williams, Ann
Dennis, Mike
Marsh, Philip D.
Sharpe, Sally
author_sort Sibley, Laura
collection PubMed
description This study describes the use of cynomolgus macaques of Chinese origin (CCM) to evaluate the efficacy and immunogenicity of the BCG vaccine against high dose aerosol Mycobacterium tuberculosis challenge. Progressive disease developed in three of the unvaccinated animals within 10 weeks of challenge, whereas all six vaccinated animals controlled disease for 26 weeks. Three unvaccinated animals limited disease progression, highlighting the intrinsic ability of this macaque species to control disease in comparison to macaques of other species and genotypes. Low levels of IFNγ were induced by BCG vaccination in CCM suggesting that IFNγ alone does not provide a sufficiently sensitive biomarker of vaccination in this model. An early response after challenge, together with the natural bias towards terminal effector memory T-cell populations and the contribution of monocytes appears to enhance the ability of CCM to naturally control infection. The high dose aerosol challenge model of CCM has value for examination of the host immune system to characterise control of infection which would influence future vaccine design. Although it may not be the preferred platform for the assessment of prophylactic vaccine candidates, the model could be well suited for testing post-exposure vaccination strategies and drug evaluation studies.
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spelling pubmed-81929092021-06-14 High-dose Mycobacterium tuberculosis aerosol challenge cannot overcome BCG-induced protection in Chinese origin cynomolgus macaques; implications of natural resistance for vaccine evaluation Sibley, Laura White, Andrew D. Gooch, Karen E. Stevens, Lisa M. Tanner, Rachel Jacobs, Ashley Daykin-Pont, Owen Gleeson, Fergus McIntyre, Anthony Basaraba, Randall Clark, Simon Hall, Graham Pearson, Geoff Rayner, Emma McShane, Helen Williams, Ann Dennis, Mike Marsh, Philip D. Sharpe, Sally Sci Rep Article This study describes the use of cynomolgus macaques of Chinese origin (CCM) to evaluate the efficacy and immunogenicity of the BCG vaccine against high dose aerosol Mycobacterium tuberculosis challenge. Progressive disease developed in three of the unvaccinated animals within 10 weeks of challenge, whereas all six vaccinated animals controlled disease for 26 weeks. Three unvaccinated animals limited disease progression, highlighting the intrinsic ability of this macaque species to control disease in comparison to macaques of other species and genotypes. Low levels of IFNγ were induced by BCG vaccination in CCM suggesting that IFNγ alone does not provide a sufficiently sensitive biomarker of vaccination in this model. An early response after challenge, together with the natural bias towards terminal effector memory T-cell populations and the contribution of monocytes appears to enhance the ability of CCM to naturally control infection. The high dose aerosol challenge model of CCM has value for examination of the host immune system to characterise control of infection which would influence future vaccine design. Although it may not be the preferred platform for the assessment of prophylactic vaccine candidates, the model could be well suited for testing post-exposure vaccination strategies and drug evaluation studies. Nature Publishing Group UK 2021-06-10 /pmc/articles/PMC8192909/ /pubmed/34112845 http://dx.doi.org/10.1038/s41598-021-90913-0 Text en © Crown 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sibley, Laura
White, Andrew D.
Gooch, Karen E.
Stevens, Lisa M.
Tanner, Rachel
Jacobs, Ashley
Daykin-Pont, Owen
Gleeson, Fergus
McIntyre, Anthony
Basaraba, Randall
Clark, Simon
Hall, Graham
Pearson, Geoff
Rayner, Emma
McShane, Helen
Williams, Ann
Dennis, Mike
Marsh, Philip D.
Sharpe, Sally
High-dose Mycobacterium tuberculosis aerosol challenge cannot overcome BCG-induced protection in Chinese origin cynomolgus macaques; implications of natural resistance for vaccine evaluation
title High-dose Mycobacterium tuberculosis aerosol challenge cannot overcome BCG-induced protection in Chinese origin cynomolgus macaques; implications of natural resistance for vaccine evaluation
title_full High-dose Mycobacterium tuberculosis aerosol challenge cannot overcome BCG-induced protection in Chinese origin cynomolgus macaques; implications of natural resistance for vaccine evaluation
title_fullStr High-dose Mycobacterium tuberculosis aerosol challenge cannot overcome BCG-induced protection in Chinese origin cynomolgus macaques; implications of natural resistance for vaccine evaluation
title_full_unstemmed High-dose Mycobacterium tuberculosis aerosol challenge cannot overcome BCG-induced protection in Chinese origin cynomolgus macaques; implications of natural resistance for vaccine evaluation
title_short High-dose Mycobacterium tuberculosis aerosol challenge cannot overcome BCG-induced protection in Chinese origin cynomolgus macaques; implications of natural resistance for vaccine evaluation
title_sort high-dose mycobacterium tuberculosis aerosol challenge cannot overcome bcg-induced protection in chinese origin cynomolgus macaques; implications of natural resistance for vaccine evaluation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192909/
https://www.ncbi.nlm.nih.gov/pubmed/34112845
http://dx.doi.org/10.1038/s41598-021-90913-0
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