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Subcutaneous BCG vaccination protects against streptococcal pneumonia via regulating innate immune responses in the lung
Bacillus Calmette‐Guérin (BCG) still remains the only licensed vaccine for TB and has been shown to provide nonspecific protection against unrelated pathogens. This has been attributed to the ability of BCG to modulate the innate immune system, known as trained innate immunity (TII). Trained innate...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331578/ https://www.ncbi.nlm.nih.gov/pubmed/37158369 http://dx.doi.org/10.15252/emmm.202217084 |
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author | Kang, Alisha Ye, Gluke Singh, Ramandeep Afkhami, Sam Bavananthasivam, Jegarubee Luo, Xiangqian Vaseghi‐Shanjani, Maryam Aleithan, Fatemah Zganiacz, Anna Jeyanathan, Mangalakumari Xing, Zhou |
author_facet | Kang, Alisha Ye, Gluke Singh, Ramandeep Afkhami, Sam Bavananthasivam, Jegarubee Luo, Xiangqian Vaseghi‐Shanjani, Maryam Aleithan, Fatemah Zganiacz, Anna Jeyanathan, Mangalakumari Xing, Zhou |
author_sort | Kang, Alisha |
collection | PubMed |
description | Bacillus Calmette‐Guérin (BCG) still remains the only licensed vaccine for TB and has been shown to provide nonspecific protection against unrelated pathogens. This has been attributed to the ability of BCG to modulate the innate immune system, known as trained innate immunity (TII). Trained innate immunity is associated with innate immune cells being in a hyperresponsive state leading to enhanced host defense against heterologous infections. Both epidemiological evidence and prospective studies demonstrate cutaneous BCG vaccine‐induced TII provides enhanced innate protection against heterologous pathogens. Regardless of the extensive progress made thus far, the effect of cutaneous BCG vaccination against heterologous respiratory bacterial infections and the underlying mechanisms still remain unknown. Here, we show that s.c. BCG vaccine‐induced TII provides enhanced heterologous innate protection against pulmonary Streptococcus pneumoniae infection. We further demonstrate that this enhanced innate protection is mediated by enhanced neutrophilia in the lung and is independent of centrally trained circulating monocytes. New insight from this study will help design novel effective vaccination strategies against unrelated respiratory bacterial pathogens. |
format | Online Article Text |
id | pubmed-10331578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103315782023-07-11 Subcutaneous BCG vaccination protects against streptococcal pneumonia via regulating innate immune responses in the lung Kang, Alisha Ye, Gluke Singh, Ramandeep Afkhami, Sam Bavananthasivam, Jegarubee Luo, Xiangqian Vaseghi‐Shanjani, Maryam Aleithan, Fatemah Zganiacz, Anna Jeyanathan, Mangalakumari Xing, Zhou EMBO Mol Med Articles Bacillus Calmette‐Guérin (BCG) still remains the only licensed vaccine for TB and has been shown to provide nonspecific protection against unrelated pathogens. This has been attributed to the ability of BCG to modulate the innate immune system, known as trained innate immunity (TII). Trained innate immunity is associated with innate immune cells being in a hyperresponsive state leading to enhanced host defense against heterologous infections. Both epidemiological evidence and prospective studies demonstrate cutaneous BCG vaccine‐induced TII provides enhanced innate protection against heterologous pathogens. Regardless of the extensive progress made thus far, the effect of cutaneous BCG vaccination against heterologous respiratory bacterial infections and the underlying mechanisms still remain unknown. Here, we show that s.c. BCG vaccine‐induced TII provides enhanced heterologous innate protection against pulmonary Streptococcus pneumoniae infection. We further demonstrate that this enhanced innate protection is mediated by enhanced neutrophilia in the lung and is independent of centrally trained circulating monocytes. New insight from this study will help design novel effective vaccination strategies against unrelated respiratory bacterial pathogens. John Wiley and Sons Inc. 2023-05-09 /pmc/articles/PMC10331578/ /pubmed/37158369 http://dx.doi.org/10.15252/emmm.202217084 Text en © 2023 The Authors. Published under the terms of the CC BY 4.0 license. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Kang, Alisha Ye, Gluke Singh, Ramandeep Afkhami, Sam Bavananthasivam, Jegarubee Luo, Xiangqian Vaseghi‐Shanjani, Maryam Aleithan, Fatemah Zganiacz, Anna Jeyanathan, Mangalakumari Xing, Zhou Subcutaneous BCG vaccination protects against streptococcal pneumonia via regulating innate immune responses in the lung |
title | Subcutaneous BCG vaccination protects against streptococcal pneumonia via regulating innate immune responses in the lung |
title_full | Subcutaneous BCG vaccination protects against streptococcal pneumonia via regulating innate immune responses in the lung |
title_fullStr | Subcutaneous BCG vaccination protects against streptococcal pneumonia via regulating innate immune responses in the lung |
title_full_unstemmed | Subcutaneous BCG vaccination protects against streptococcal pneumonia via regulating innate immune responses in the lung |
title_short | Subcutaneous BCG vaccination protects against streptococcal pneumonia via regulating innate immune responses in the lung |
title_sort | subcutaneous bcg vaccination protects against streptococcal pneumonia via regulating innate immune responses in the lung |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331578/ https://www.ncbi.nlm.nih.gov/pubmed/37158369 http://dx.doi.org/10.15252/emmm.202217084 |
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