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Immunometabolism in biofilm infection: lessons from cancer
BACKGROUND: Biofilm is a community of bacteria embedded in an extracellular matrix, which can colonize different human cells and tissues and subvert the host immune reactions by preventing immune detection and polarizing the immune reactions towards an anti-inflammatory state, promoting the persiste...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800364/ https://www.ncbi.nlm.nih.gov/pubmed/35093033 http://dx.doi.org/10.1186/s10020-022-00435-2 |
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author | Mirzaei, Rasoul Sabokroo, Niloofar Ahmadyousefi, Yaghoub Motamedi, Hamid Karampoor, Sajad |
author_facet | Mirzaei, Rasoul Sabokroo, Niloofar Ahmadyousefi, Yaghoub Motamedi, Hamid Karampoor, Sajad |
author_sort | Mirzaei, Rasoul |
collection | PubMed |
description | BACKGROUND: Biofilm is a community of bacteria embedded in an extracellular matrix, which can colonize different human cells and tissues and subvert the host immune reactions by preventing immune detection and polarizing the immune reactions towards an anti-inflammatory state, promoting the persistence of biofilm-embedded bacteria in the host. MAIN BODY OF THE MANUSCRIPT: It is now well established that the function of immune cells is ultimately mediated by cellular metabolism. The immune cells are stimulated to regulate their immune functions upon sensing danger signals. Recent studies have determined that immune cells often display distinct metabolic alterations that impair their immune responses when triggered. Such metabolic reprogramming and its physiological implications are well established in cancer situations. In bacterial infections, immuno-metabolic evaluations have primarily focused on macrophages and neutrophils in the planktonic growth mode. CONCLUSION: Based on differences in inflammatory reactions of macrophages and neutrophils in planktonic- versus biofilm-associated bacterial infections, studies must also consider the metabolic functions of immune cells against biofilm infections. The profound characterization of the metabolic and immune cell reactions could offer exciting novel targets for antibiofilm therapy. |
format | Online Article Text |
id | pubmed-8800364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88003642022-02-01 Immunometabolism in biofilm infection: lessons from cancer Mirzaei, Rasoul Sabokroo, Niloofar Ahmadyousefi, Yaghoub Motamedi, Hamid Karampoor, Sajad Mol Med Review BACKGROUND: Biofilm is a community of bacteria embedded in an extracellular matrix, which can colonize different human cells and tissues and subvert the host immune reactions by preventing immune detection and polarizing the immune reactions towards an anti-inflammatory state, promoting the persistence of biofilm-embedded bacteria in the host. MAIN BODY OF THE MANUSCRIPT: It is now well established that the function of immune cells is ultimately mediated by cellular metabolism. The immune cells are stimulated to regulate their immune functions upon sensing danger signals. Recent studies have determined that immune cells often display distinct metabolic alterations that impair their immune responses when triggered. Such metabolic reprogramming and its physiological implications are well established in cancer situations. In bacterial infections, immuno-metabolic evaluations have primarily focused on macrophages and neutrophils in the planktonic growth mode. CONCLUSION: Based on differences in inflammatory reactions of macrophages and neutrophils in planktonic- versus biofilm-associated bacterial infections, studies must also consider the metabolic functions of immune cells against biofilm infections. The profound characterization of the metabolic and immune cell reactions could offer exciting novel targets for antibiofilm therapy. BioMed Central 2022-01-29 /pmc/articles/PMC8800364/ /pubmed/35093033 http://dx.doi.org/10.1186/s10020-022-00435-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Mirzaei, Rasoul Sabokroo, Niloofar Ahmadyousefi, Yaghoub Motamedi, Hamid Karampoor, Sajad Immunometabolism in biofilm infection: lessons from cancer |
title | Immunometabolism in biofilm infection: lessons from cancer |
title_full | Immunometabolism in biofilm infection: lessons from cancer |
title_fullStr | Immunometabolism in biofilm infection: lessons from cancer |
title_full_unstemmed | Immunometabolism in biofilm infection: lessons from cancer |
title_short | Immunometabolism in biofilm infection: lessons from cancer |
title_sort | immunometabolism in biofilm infection: lessons from cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800364/ https://www.ncbi.nlm.nih.gov/pubmed/35093033 http://dx.doi.org/10.1186/s10020-022-00435-2 |
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