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MTBVAC vaccination protects rhesus macaques against aerosol challenge with M. tuberculosis and induces immune signatures analogous to those observed in clinical studies

A single intradermal vaccination with MTBVAC given to adult rhesus macaques was well tolerated and conferred a significant improvement in outcome following aerosol exposure to M. tuberculosis compared to that provided by a single BCG vaccination. Vaccination with MTBVAC resulted in a significant red...

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Autores principales: White, Andrew D., Sibley, Laura, Sarfas, Charlotte, Morrison, Alexandra, Gullick, Jennie, Clark, Simon, Gleeson, Fergus, McIntyre, Anthony, Arlehamn, Cecilia Lindestam, Sette, Alessandro, Salguero, Francisco J., Rayner, Emma, Rodriguez, Esteban, Puentes, Eugenia, Laddy, Dominick, Williams, Ann, Dennis, Mike, Martin, Carlos, 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/PMC7782851/
https://www.ncbi.nlm.nih.gov/pubmed/33397991
http://dx.doi.org/10.1038/s41541-020-00262-8
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author White, Andrew D.
Sibley, Laura
Sarfas, Charlotte
Morrison, Alexandra
Gullick, Jennie
Clark, Simon
Gleeson, Fergus
McIntyre, Anthony
Arlehamn, Cecilia Lindestam
Sette, Alessandro
Salguero, Francisco J.
Rayner, Emma
Rodriguez, Esteban
Puentes, Eugenia
Laddy, Dominick
Williams, Ann
Dennis, Mike
Martin, Carlos
Sharpe, Sally
author_facet White, Andrew D.
Sibley, Laura
Sarfas, Charlotte
Morrison, Alexandra
Gullick, Jennie
Clark, Simon
Gleeson, Fergus
McIntyre, Anthony
Arlehamn, Cecilia Lindestam
Sette, Alessandro
Salguero, Francisco J.
Rayner, Emma
Rodriguez, Esteban
Puentes, Eugenia
Laddy, Dominick
Williams, Ann
Dennis, Mike
Martin, Carlos
Sharpe, Sally
author_sort White, Andrew D.
collection PubMed
description A single intradermal vaccination with MTBVAC given to adult rhesus macaques was well tolerated and conferred a significant improvement in outcome following aerosol exposure to M. tuberculosis compared to that provided by a single BCG vaccination. Vaccination with MTBVAC resulted in a significant reduction in M. tuberculosis infection-induced disease pathology measured using in vivo medical imaging, in gross pathology lesion counts and pathology scores recorded at necropsy, the frequency and severity of pulmonary granulomas and the frequency of recovery of viable M. tuberculosis from extrapulmonary tissues following challenge. The immune profiles induced following immunisation with MTBVAC reflect those identified in human clinical trials of MTBVAC. Evaluation of MTBVAC- and TB peptide-pool-specific T-cell cytokine production revealed a predominantly Th1 response from poly- (IFN-γ(+)TNF-α(+)IL2(+)) and multi-(IFN-γ(+)TNF-α(+)) functional CD4 T cells, while only low levels of Th22, Th17 and cytokine-producing CD8 T-cell populations were detected together with low-level, but significant, increases in CFP10-specific IFN-γ secreting cells. In this report, we describe concordance between immune profiles measured in clinical trials and a macaque pre-clinical study demonstrating significantly improved outcome after M. tuberculosis challenge as evidence to support the continued development of MTBVAC as an effective prophylactic vaccine for TB vaccination campaigns.
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spelling pubmed-77828512021-01-14 MTBVAC vaccination protects rhesus macaques against aerosol challenge with M. tuberculosis and induces immune signatures analogous to those observed in clinical studies White, Andrew D. Sibley, Laura Sarfas, Charlotte Morrison, Alexandra Gullick, Jennie Clark, Simon Gleeson, Fergus McIntyre, Anthony Arlehamn, Cecilia Lindestam Sette, Alessandro Salguero, Francisco J. Rayner, Emma Rodriguez, Esteban Puentes, Eugenia Laddy, Dominick Williams, Ann Dennis, Mike Martin, Carlos Sharpe, Sally NPJ Vaccines Article A single intradermal vaccination with MTBVAC given to adult rhesus macaques was well tolerated and conferred a significant improvement in outcome following aerosol exposure to M. tuberculosis compared to that provided by a single BCG vaccination. Vaccination with MTBVAC resulted in a significant reduction in M. tuberculosis infection-induced disease pathology measured using in vivo medical imaging, in gross pathology lesion counts and pathology scores recorded at necropsy, the frequency and severity of pulmonary granulomas and the frequency of recovery of viable M. tuberculosis from extrapulmonary tissues following challenge. The immune profiles induced following immunisation with MTBVAC reflect those identified in human clinical trials of MTBVAC. Evaluation of MTBVAC- and TB peptide-pool-specific T-cell cytokine production revealed a predominantly Th1 response from poly- (IFN-γ(+)TNF-α(+)IL2(+)) and multi-(IFN-γ(+)TNF-α(+)) functional CD4 T cells, while only low levels of Th22, Th17 and cytokine-producing CD8 T-cell populations were detected together with low-level, but significant, increases in CFP10-specific IFN-γ secreting cells. In this report, we describe concordance between immune profiles measured in clinical trials and a macaque pre-clinical study demonstrating significantly improved outcome after M. tuberculosis challenge as evidence to support the continued development of MTBVAC as an effective prophylactic vaccine for TB vaccination campaigns. Nature Publishing Group UK 2021-01-04 /pmc/articles/PMC7782851/ /pubmed/33397991 http://dx.doi.org/10.1038/s41541-020-00262-8 Text en © Crown 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
White, Andrew D.
Sibley, Laura
Sarfas, Charlotte
Morrison, Alexandra
Gullick, Jennie
Clark, Simon
Gleeson, Fergus
McIntyre, Anthony
Arlehamn, Cecilia Lindestam
Sette, Alessandro
Salguero, Francisco J.
Rayner, Emma
Rodriguez, Esteban
Puentes, Eugenia
Laddy, Dominick
Williams, Ann
Dennis, Mike
Martin, Carlos
Sharpe, Sally
MTBVAC vaccination protects rhesus macaques against aerosol challenge with M. tuberculosis and induces immune signatures analogous to those observed in clinical studies
title MTBVAC vaccination protects rhesus macaques against aerosol challenge with M. tuberculosis and induces immune signatures analogous to those observed in clinical studies
title_full MTBVAC vaccination protects rhesus macaques against aerosol challenge with M. tuberculosis and induces immune signatures analogous to those observed in clinical studies
title_fullStr MTBVAC vaccination protects rhesus macaques against aerosol challenge with M. tuberculosis and induces immune signatures analogous to those observed in clinical studies
title_full_unstemmed MTBVAC vaccination protects rhesus macaques against aerosol challenge with M. tuberculosis and induces immune signatures analogous to those observed in clinical studies
title_short MTBVAC vaccination protects rhesus macaques against aerosol challenge with M. tuberculosis and induces immune signatures analogous to those observed in clinical studies
title_sort mtbvac vaccination protects rhesus macaques against aerosol challenge with m. tuberculosis and induces immune signatures analogous to those observed in clinical studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782851/
https://www.ncbi.nlm.nih.gov/pubmed/33397991
http://dx.doi.org/10.1038/s41541-020-00262-8
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