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Lessons from Bacillus Calmette-Guérin: Harnessing Trained Immunity for Vaccine Development

Vaccine design traditionally focuses on inducing adaptive immune responses against a sole target pathogen. Considering that many microbes evade innate immune mechanisms to initiate infection, and in light of the discovery of epigenetically mediated innate immune training, the paradigm of vaccine des...

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Detalles Bibliográficos
Autores principales: Pasco, Samuel T., Anguita, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564904/
https://www.ncbi.nlm.nih.gov/pubmed/32948003
http://dx.doi.org/10.3390/cells9092109
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author Pasco, Samuel T.
Anguita, Juan
author_facet Pasco, Samuel T.
Anguita, Juan
author_sort Pasco, Samuel T.
collection PubMed
description Vaccine design traditionally focuses on inducing adaptive immune responses against a sole target pathogen. Considering that many microbes evade innate immune mechanisms to initiate infection, and in light of the discovery of epigenetically mediated innate immune training, the paradigm of vaccine design has the potential to change. The Bacillus Calmette-Guérin (BCG) vaccine induces some level of protection against Mycobacterium tuberculosis (Mtb) while stimulating trained immunity that correlates with lower mortality and increased protection against unrelated pathogens. This review will explore BCG-induced trained immunity, including the required pathways to establish this phenotype. Additionally, potential methods to improve or expand BCG trained immunity effects through alternative vaccine delivery and formulation methods will be discussed. Finally, advances in new anti-Mtb vaccines, other antimicrobial uses for BCG, and “innate memory-based vaccines” will be examined.
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spelling pubmed-75649042020-10-26 Lessons from Bacillus Calmette-Guérin: Harnessing Trained Immunity for Vaccine Development Pasco, Samuel T. Anguita, Juan Cells Review Vaccine design traditionally focuses on inducing adaptive immune responses against a sole target pathogen. Considering that many microbes evade innate immune mechanisms to initiate infection, and in light of the discovery of epigenetically mediated innate immune training, the paradigm of vaccine design has the potential to change. The Bacillus Calmette-Guérin (BCG) vaccine induces some level of protection against Mycobacterium tuberculosis (Mtb) while stimulating trained immunity that correlates with lower mortality and increased protection against unrelated pathogens. This review will explore BCG-induced trained immunity, including the required pathways to establish this phenotype. Additionally, potential methods to improve or expand BCG trained immunity effects through alternative vaccine delivery and formulation methods will be discussed. Finally, advances in new anti-Mtb vaccines, other antimicrobial uses for BCG, and “innate memory-based vaccines” will be examined. MDPI 2020-09-16 /pmc/articles/PMC7564904/ /pubmed/32948003 http://dx.doi.org/10.3390/cells9092109 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pasco, Samuel T.
Anguita, Juan
Lessons from Bacillus Calmette-Guérin: Harnessing Trained Immunity for Vaccine Development
title Lessons from Bacillus Calmette-Guérin: Harnessing Trained Immunity for Vaccine Development
title_full Lessons from Bacillus Calmette-Guérin: Harnessing Trained Immunity for Vaccine Development
title_fullStr Lessons from Bacillus Calmette-Guérin: Harnessing Trained Immunity for Vaccine Development
title_full_unstemmed Lessons from Bacillus Calmette-Guérin: Harnessing Trained Immunity for Vaccine Development
title_short Lessons from Bacillus Calmette-Guérin: Harnessing Trained Immunity for Vaccine Development
title_sort lessons from bacillus calmette-guérin: harnessing trained immunity for vaccine development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564904/
https://www.ncbi.nlm.nih.gov/pubmed/32948003
http://dx.doi.org/10.3390/cells9092109
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