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BCG vaccine and COVID-19: implications for infection prophylaxis and cancer immunotherapy
The COVID-19 pandemic has killed over 400 000 people globally. Ecological evidence indicates that countries with national universal BCG vaccination programs for tuberculosis (TB) prevention have a much lower incidence of severe COVID-19 and mortality compared with those that do not have such program...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342862/ https://www.ncbi.nlm.nih.gov/pubmed/32636240 http://dx.doi.org/10.1136/jitc-2020-001119 |
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author | Koti, Madhuri Morales, Alvaro Graham, Charles H Siemens, David Robert |
author_facet | Koti, Madhuri Morales, Alvaro Graham, Charles H Siemens, David Robert |
author_sort | Koti, Madhuri |
collection | PubMed |
description | The COVID-19 pandemic has killed over 400 000 people globally. Ecological evidence indicates that countries with national universal BCG vaccination programs for tuberculosis (TB) prevention have a much lower incidence of severe COVID-19 and mortality compared with those that do not have such programs. BCG is a century old vaccine used for TB prevention via infant/childhood vaccination in lowto middle-income countries with high infection prevalence rate and is known to reduce all-cause neonatal mortality. BCG remains the standard immunotherapy treatment for patients with high-risk non-muscle invasive bladder cancer globally for more than 44 years. Several trials are, therefore, investigating BCG as a prophylactic against COVID-19 in healthcare workers and the elderly. In this commentary, we discuss the potential mechanisms that may underlie BCG associated heterologous protection with a focus on tertiary lymphoid structure (TLS) organogenesis. Given the significance of TLSs in mucosal immunity, their association with positive prognosis and response to immune checkpoint blockade with a critical role of Type I interferon (IFN-1) in inducing these, we also discuss potentiating TLS formation as a promising approach to enhance anti-tumor immunity. We propose that lessons learned from BCG immunotherapy success could be applied to not only augment such microbe-based therapeutics but also lead to similar adjunctive IFN-1 activating approaches to improve response to immune checkpoint blockade therapy in cancer. |
format | Online Article Text |
id | pubmed-7342862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-73428622020-07-09 BCG vaccine and COVID-19: implications for infection prophylaxis and cancer immunotherapy Koti, Madhuri Morales, Alvaro Graham, Charles H Siemens, David Robert J Immunother Cancer Commentary The COVID-19 pandemic has killed over 400 000 people globally. Ecological evidence indicates that countries with national universal BCG vaccination programs for tuberculosis (TB) prevention have a much lower incidence of severe COVID-19 and mortality compared with those that do not have such programs. BCG is a century old vaccine used for TB prevention via infant/childhood vaccination in lowto middle-income countries with high infection prevalence rate and is known to reduce all-cause neonatal mortality. BCG remains the standard immunotherapy treatment for patients with high-risk non-muscle invasive bladder cancer globally for more than 44 years. Several trials are, therefore, investigating BCG as a prophylactic against COVID-19 in healthcare workers and the elderly. In this commentary, we discuss the potential mechanisms that may underlie BCG associated heterologous protection with a focus on tertiary lymphoid structure (TLS) organogenesis. Given the significance of TLSs in mucosal immunity, their association with positive prognosis and response to immune checkpoint blockade with a critical role of Type I interferon (IFN-1) in inducing these, we also discuss potentiating TLS formation as a promising approach to enhance anti-tumor immunity. We propose that lessons learned from BCG immunotherapy success could be applied to not only augment such microbe-based therapeutics but also lead to similar adjunctive IFN-1 activating approaches to improve response to immune checkpoint blockade therapy in cancer. BMJ Publishing Group 2020-07-06 /pmc/articles/PMC7342862/ /pubmed/32636240 http://dx.doi.org/10.1136/jitc-2020-001119 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Commentary Koti, Madhuri Morales, Alvaro Graham, Charles H Siemens, David Robert BCG vaccine and COVID-19: implications for infection prophylaxis and cancer immunotherapy |
title | BCG vaccine and COVID-19: implications for infection prophylaxis and cancer immunotherapy |
title_full | BCG vaccine and COVID-19: implications for infection prophylaxis and cancer immunotherapy |
title_fullStr | BCG vaccine and COVID-19: implications for infection prophylaxis and cancer immunotherapy |
title_full_unstemmed | BCG vaccine and COVID-19: implications for infection prophylaxis and cancer immunotherapy |
title_short | BCG vaccine and COVID-19: implications for infection prophylaxis and cancer immunotherapy |
title_sort | bcg vaccine and covid-19: implications for infection prophylaxis and cancer immunotherapy |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342862/ https://www.ncbi.nlm.nih.gov/pubmed/32636240 http://dx.doi.org/10.1136/jitc-2020-001119 |
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