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Trained immunity as a novel approach against COVID‐19 with a focus on Bacillus Calmette–Guérin vaccine: mechanisms, challenges and perspectives

COVID‐19 is a severe health problem in many countries and has altered day‐to‐day life in the whole world. This infection is caused by the SARS‐CoV‐2 virus, and depending on age, sex and health status of the patient, it can present with variety of clinical symptoms such as mild infection, a very seve...

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Autores principales: Sohrabi, Yahya, Dos Santos, Jéssica Cristina, Dorenkamp, Marc, Findeisen, Hannes, Godfrey, Rinesh, Netea, Mihai G, Joosten, Leo AB
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755499/
https://www.ncbi.nlm.nih.gov/pubmed/33363733
http://dx.doi.org/10.1002/cti2.1228
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author Sohrabi, Yahya
Dos Santos, Jéssica Cristina
Dorenkamp, Marc
Findeisen, Hannes
Godfrey, Rinesh
Netea, Mihai G
Joosten, Leo AB
author_facet Sohrabi, Yahya
Dos Santos, Jéssica Cristina
Dorenkamp, Marc
Findeisen, Hannes
Godfrey, Rinesh
Netea, Mihai G
Joosten, Leo AB
author_sort Sohrabi, Yahya
collection PubMed
description COVID‐19 is a severe health problem in many countries and has altered day‐to‐day life in the whole world. This infection is caused by the SARS‐CoV‐2 virus, and depending on age, sex and health status of the patient, it can present with variety of clinical symptoms such as mild infection, a very severe form or even asymptomatic course of the disease. Similarly to other viruses, innate immune response plays a vital role in protection against COVID‐19. However, dysregulation of innate immunity could have a significant influence on the severity of the disease. Despite various efforts, there is no effective vaccine against the disease so far. Recent data have demonstrated that the Bacillus Calmette–Guérin (BCG) vaccine could reduce disease severity and the burden of several infectious diseases in addition to targeting its primary focus tuberculosis. There is growing evidence for the concept of beneficial non‐specific boosting of immune responses by BCG or other microbial compounds termed trained immunity, which may protect against COVID‐19. In this manuscript, we review data on how the development of innate immune memory due to microbial compounds specifically BCG can result in protection against SARS‐CoV‐2 infection. We also discuss possible mechanisms, challenges and perspectives of using innate immunity as an approach to reduce COVID‐19 severity.
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spelling pubmed-77554992020-12-23 Trained immunity as a novel approach against COVID‐19 with a focus on Bacillus Calmette–Guérin vaccine: mechanisms, challenges and perspectives Sohrabi, Yahya Dos Santos, Jéssica Cristina Dorenkamp, Marc Findeisen, Hannes Godfrey, Rinesh Netea, Mihai G Joosten, Leo AB Clin Transl Immunology Reviews COVID‐19 is a severe health problem in many countries and has altered day‐to‐day life in the whole world. This infection is caused by the SARS‐CoV‐2 virus, and depending on age, sex and health status of the patient, it can present with variety of clinical symptoms such as mild infection, a very severe form or even asymptomatic course of the disease. Similarly to other viruses, innate immune response plays a vital role in protection against COVID‐19. However, dysregulation of innate immunity could have a significant influence on the severity of the disease. Despite various efforts, there is no effective vaccine against the disease so far. Recent data have demonstrated that the Bacillus Calmette–Guérin (BCG) vaccine could reduce disease severity and the burden of several infectious diseases in addition to targeting its primary focus tuberculosis. There is growing evidence for the concept of beneficial non‐specific boosting of immune responses by BCG or other microbial compounds termed trained immunity, which may protect against COVID‐19. In this manuscript, we review data on how the development of innate immune memory due to microbial compounds specifically BCG can result in protection against SARS‐CoV‐2 infection. We also discuss possible mechanisms, challenges and perspectives of using innate immunity as an approach to reduce COVID‐19 severity. John Wiley and Sons Inc. 2020-12-22 /pmc/articles/PMC7755499/ /pubmed/33363733 http://dx.doi.org/10.1002/cti2.1228 Text en © 2020 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reviews
Sohrabi, Yahya
Dos Santos, Jéssica Cristina
Dorenkamp, Marc
Findeisen, Hannes
Godfrey, Rinesh
Netea, Mihai G
Joosten, Leo AB
Trained immunity as a novel approach against COVID‐19 with a focus on Bacillus Calmette–Guérin vaccine: mechanisms, challenges and perspectives
title Trained immunity as a novel approach against COVID‐19 with a focus on Bacillus Calmette–Guérin vaccine: mechanisms, challenges and perspectives
title_full Trained immunity as a novel approach against COVID‐19 with a focus on Bacillus Calmette–Guérin vaccine: mechanisms, challenges and perspectives
title_fullStr Trained immunity as a novel approach against COVID‐19 with a focus on Bacillus Calmette–Guérin vaccine: mechanisms, challenges and perspectives
title_full_unstemmed Trained immunity as a novel approach against COVID‐19 with a focus on Bacillus Calmette–Guérin vaccine: mechanisms, challenges and perspectives
title_short Trained immunity as a novel approach against COVID‐19 with a focus on Bacillus Calmette–Guérin vaccine: mechanisms, challenges and perspectives
title_sort trained immunity as a novel approach against covid‐19 with a focus on bacillus calmette–guérin vaccine: mechanisms, challenges and perspectives
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755499/
https://www.ncbi.nlm.nih.gov/pubmed/33363733
http://dx.doi.org/10.1002/cti2.1228
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