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Vaginal Lactobacilli and Vaginal Dysbiosis-Associated Bacteria Differently Affect Cervical Epithelial and Immune Homeostasis and Anti-Viral Defenses

Persistent infection with High Risk-Human Papilloma Viruses (HR-HPVs) is a primary cause of cervical cancer worldwide. Vaginal-dysbiosis-associated bacteria were correlated with the persistence of HR-HPVs infection and with increased cancer risk. We obtained strains of the most represented bacterial...

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Autores principales: Nicolò, Sabrina, Tanturli, Michele, Mattiuz, Giorgio, Antonelli, Alberto, Baccani, Ilaria, Bonaiuto, Chiara, Baldi, Simone, Nannini, Giulia, Menicatti, Marta, Bartolucci, Gianluca, Rossolini, Gian Maria, Amedei, Amedeo, Torcia, Maria Gabriella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234132/
https://www.ncbi.nlm.nih.gov/pubmed/34204294
http://dx.doi.org/10.3390/ijms22126487
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author Nicolò, Sabrina
Tanturli, Michele
Mattiuz, Giorgio
Antonelli, Alberto
Baccani, Ilaria
Bonaiuto, Chiara
Baldi, Simone
Nannini, Giulia
Menicatti, Marta
Bartolucci, Gianluca
Rossolini, Gian Maria
Amedei, Amedeo
Torcia, Maria Gabriella
author_facet Nicolò, Sabrina
Tanturli, Michele
Mattiuz, Giorgio
Antonelli, Alberto
Baccani, Ilaria
Bonaiuto, Chiara
Baldi, Simone
Nannini, Giulia
Menicatti, Marta
Bartolucci, Gianluca
Rossolini, Gian Maria
Amedei, Amedeo
Torcia, Maria Gabriella
author_sort Nicolò, Sabrina
collection PubMed
description Persistent infection with High Risk-Human Papilloma Viruses (HR-HPVs) is a primary cause of cervical cancer worldwide. Vaginal-dysbiosis-associated bacteria were correlated with the persistence of HR-HPVs infection and with increased cancer risk. We obtained strains of the most represented bacterial species in vaginal microbiota and evaluated their effects on the survival of cervical epithelial cells and immune homeostasis. The contribution of each species to supporting the antiviral response was also studied. Epithelial cell viability was affected by culture supernatants of most vaginal-dysbiosis bacteria, whereas Lactobacillus gasseri or Lactobacillus jensenii resulted in the best stimulus to induce interferon-γ (IFN-γ) production by human mononuclear cells from peripheral blood (PBMCs). Although vaginal-dysbiosis-associated bacteria induced the IFN-γ production, they were also optimal stimuli to interleukin-17 (IL-17) production. A positive correlation between IL-17 and IFN-γ secretion was observed in cultures of PBMCs with all vaginal-dysbiosis-associated bacteria suggesting that the adaptive immune response induced by these strains is not dominated by T(H)1 differentiation with reduced availability of IFN-γ, cytokine most effective in supporting virus clearance. Based on these results, we suggest that a vaginal microbiota dominated by lactobacilli, especially by L. gasseri or L. jensenii, may be able to assist immune cells with clearing HPV infection, bypasses the viral escape and restores immune homeostasis.
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spelling pubmed-82341322021-06-27 Vaginal Lactobacilli and Vaginal Dysbiosis-Associated Bacteria Differently Affect Cervical Epithelial and Immune Homeostasis and Anti-Viral Defenses Nicolò, Sabrina Tanturli, Michele Mattiuz, Giorgio Antonelli, Alberto Baccani, Ilaria Bonaiuto, Chiara Baldi, Simone Nannini, Giulia Menicatti, Marta Bartolucci, Gianluca Rossolini, Gian Maria Amedei, Amedeo Torcia, Maria Gabriella Int J Mol Sci Article Persistent infection with High Risk-Human Papilloma Viruses (HR-HPVs) is a primary cause of cervical cancer worldwide. Vaginal-dysbiosis-associated bacteria were correlated with the persistence of HR-HPVs infection and with increased cancer risk. We obtained strains of the most represented bacterial species in vaginal microbiota and evaluated their effects on the survival of cervical epithelial cells and immune homeostasis. The contribution of each species to supporting the antiviral response was also studied. Epithelial cell viability was affected by culture supernatants of most vaginal-dysbiosis bacteria, whereas Lactobacillus gasseri or Lactobacillus jensenii resulted in the best stimulus to induce interferon-γ (IFN-γ) production by human mononuclear cells from peripheral blood (PBMCs). Although vaginal-dysbiosis-associated bacteria induced the IFN-γ production, they were also optimal stimuli to interleukin-17 (IL-17) production. A positive correlation between IL-17 and IFN-γ secretion was observed in cultures of PBMCs with all vaginal-dysbiosis-associated bacteria suggesting that the adaptive immune response induced by these strains is not dominated by T(H)1 differentiation with reduced availability of IFN-γ, cytokine most effective in supporting virus clearance. Based on these results, we suggest that a vaginal microbiota dominated by lactobacilli, especially by L. gasseri or L. jensenii, may be able to assist immune cells with clearing HPV infection, bypasses the viral escape and restores immune homeostasis. MDPI 2021-06-17 /pmc/articles/PMC8234132/ /pubmed/34204294 http://dx.doi.org/10.3390/ijms22126487 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nicolò, Sabrina
Tanturli, Michele
Mattiuz, Giorgio
Antonelli, Alberto
Baccani, Ilaria
Bonaiuto, Chiara
Baldi, Simone
Nannini, Giulia
Menicatti, Marta
Bartolucci, Gianluca
Rossolini, Gian Maria
Amedei, Amedeo
Torcia, Maria Gabriella
Vaginal Lactobacilli and Vaginal Dysbiosis-Associated Bacteria Differently Affect Cervical Epithelial and Immune Homeostasis and Anti-Viral Defenses
title Vaginal Lactobacilli and Vaginal Dysbiosis-Associated Bacteria Differently Affect Cervical Epithelial and Immune Homeostasis and Anti-Viral Defenses
title_full Vaginal Lactobacilli and Vaginal Dysbiosis-Associated Bacteria Differently Affect Cervical Epithelial and Immune Homeostasis and Anti-Viral Defenses
title_fullStr Vaginal Lactobacilli and Vaginal Dysbiosis-Associated Bacteria Differently Affect Cervical Epithelial and Immune Homeostasis and Anti-Viral Defenses
title_full_unstemmed Vaginal Lactobacilli and Vaginal Dysbiosis-Associated Bacteria Differently Affect Cervical Epithelial and Immune Homeostasis and Anti-Viral Defenses
title_short Vaginal Lactobacilli and Vaginal Dysbiosis-Associated Bacteria Differently Affect Cervical Epithelial and Immune Homeostasis and Anti-Viral Defenses
title_sort vaginal lactobacilli and vaginal dysbiosis-associated bacteria differently affect cervical epithelial and immune homeostasis and anti-viral defenses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234132/
https://www.ncbi.nlm.nih.gov/pubmed/34204294
http://dx.doi.org/10.3390/ijms22126487
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