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Effects of MVA85A vaccine on tuberculosis challenge in animals: systematic review

Background: The existing Bacillus Calmette–Guérin (BCG) vaccination provides partial protection against tuberculosis (TB). The modified vaccinia ankara virus-expressing antigen 85A (MVA85A) aims to boost BCG immunity. We evaluated the animal evidence supporting the testing of MVA85A in humans. Metho...

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Autores principales: Kashangura, Rufaro, Sena, Emily S, Young, Taryn, Garner, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689998/
https://www.ncbi.nlm.nih.gov/pubmed/26351306
http://dx.doi.org/10.1093/ije/dyv142
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author Kashangura, Rufaro
Sena, Emily S
Young, Taryn
Garner, Paul
author_facet Kashangura, Rufaro
Sena, Emily S
Young, Taryn
Garner, Paul
author_sort Kashangura, Rufaro
collection PubMed
description Background: The existing Bacillus Calmette–Guérin (BCG) vaccination provides partial protection against tuberculosis (TB). The modified vaccinia ankara virus-expressing antigen 85A (MVA85A) aims to boost BCG immunity. We evaluated the animal evidence supporting the testing of MVA85A in humans. Methods: Our protocol included in vivo preclinical studies of the MVA85A booster with BCG compared with BCG alone, followed by a TB challenge. We used standard methods for systematic review of animal studies, and summarized mortality, measures of pathology and lung bacterial load. The comprehensive literature search was to September 2014. Two independent investigators assessed eligibility and performed data extraction. We assessed study quality and pooled bacteria load using random effect meta-analysis. Findings: We included eight studies in 192 animals. Three experiments were in mice, two in guinea pigs, two in macaques and one in calves. Overall, study quality was low with no randomization, baseline comparability not described and blinding not reported. For animal death (including euthanasia due to severe morbidity), studies were underpowered, and overall no benefit demonstrated. No difference was shown for lung pathology measured on an ordinal scale or bacterial load. The largest mortality trial carried out in macaques had more deaths in the MVA85A vaccine group, and was published after a trial in South Africa had started recruiting children. Conclusions: This independent assessment of the animal data does not provide evidence to support efficacy of MVA85A as a BCG booster. More rigorous conduct and reporting of preclinical research are warranted, and we believe the results of studies should be publicly available before embarking on trials in humans, irrespective of the findings.
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spelling pubmed-46899982015-12-30 Effects of MVA85A vaccine on tuberculosis challenge in animals: systematic review Kashangura, Rufaro Sena, Emily S Young, Taryn Garner, Paul Int J Epidemiol Miscellaneous Background: The existing Bacillus Calmette–Guérin (BCG) vaccination provides partial protection against tuberculosis (TB). The modified vaccinia ankara virus-expressing antigen 85A (MVA85A) aims to boost BCG immunity. We evaluated the animal evidence supporting the testing of MVA85A in humans. Methods: Our protocol included in vivo preclinical studies of the MVA85A booster with BCG compared with BCG alone, followed by a TB challenge. We used standard methods for systematic review of animal studies, and summarized mortality, measures of pathology and lung bacterial load. The comprehensive literature search was to September 2014. Two independent investigators assessed eligibility and performed data extraction. We assessed study quality and pooled bacteria load using random effect meta-analysis. Findings: We included eight studies in 192 animals. Three experiments were in mice, two in guinea pigs, two in macaques and one in calves. Overall, study quality was low with no randomization, baseline comparability not described and blinding not reported. For animal death (including euthanasia due to severe morbidity), studies were underpowered, and overall no benefit demonstrated. No difference was shown for lung pathology measured on an ordinal scale or bacterial load. The largest mortality trial carried out in macaques had more deaths in the MVA85A vaccine group, and was published after a trial in South Africa had started recruiting children. Conclusions: This independent assessment of the animal data does not provide evidence to support efficacy of MVA85A as a BCG booster. More rigorous conduct and reporting of preclinical research are warranted, and we believe the results of studies should be publicly available before embarking on trials in humans, irrespective of the findings. Oxford University Press 2015-12 2015-09-08 /pmc/articles/PMC4689998/ /pubmed/26351306 http://dx.doi.org/10.1093/ije/dyv142 Text en © The Author 2015. Published by Oxford University Press on behalf of the International Epidemiological Association http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Miscellaneous
Kashangura, Rufaro
Sena, Emily S
Young, Taryn
Garner, Paul
Effects of MVA85A vaccine on tuberculosis challenge in animals: systematic review
title Effects of MVA85A vaccine on tuberculosis challenge in animals: systematic review
title_full Effects of MVA85A vaccine on tuberculosis challenge in animals: systematic review
title_fullStr Effects of MVA85A vaccine on tuberculosis challenge in animals: systematic review
title_full_unstemmed Effects of MVA85A vaccine on tuberculosis challenge in animals: systematic review
title_short Effects of MVA85A vaccine on tuberculosis challenge in animals: systematic review
title_sort effects of mva85a vaccine on tuberculosis challenge in animals: systematic review
topic Miscellaneous
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689998/
https://www.ncbi.nlm.nih.gov/pubmed/26351306
http://dx.doi.org/10.1093/ije/dyv142
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