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Selective Activation of Human Dendritic Cells by OM-85 through a NF-kB and MAPK Dependent Pathway

OM-85 (Broncho-Vaxom®, Broncho-Munal®, Ommunal®, Paxoral®, Vaxoral®), a product made of the water soluble fractions of 21 inactivated bacterial strain patterns responsible for respiratory tract infections, is used for the prevention of recurrent upper respiratory tract infections and acute exacerbat...

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Autores principales: Parola, Carmen, Salogni, Laura, Vaira, Xenia, Scutera, Sara, Somma, Paolo, Salvi, Valentina, Musso, Tiziana, Tabbia, Giuseppe, Bardessono, Marco, Pasquali, Christian, Mantovani, Alberto, Sozzani, Silvano, Bosisio, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875422/
https://www.ncbi.nlm.nih.gov/pubmed/24386121
http://dx.doi.org/10.1371/journal.pone.0082867
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author Parola, Carmen
Salogni, Laura
Vaira, Xenia
Scutera, Sara
Somma, Paolo
Salvi, Valentina
Musso, Tiziana
Tabbia, Giuseppe
Bardessono, Marco
Pasquali, Christian
Mantovani, Alberto
Sozzani, Silvano
Bosisio, Daniela
author_facet Parola, Carmen
Salogni, Laura
Vaira, Xenia
Scutera, Sara
Somma, Paolo
Salvi, Valentina
Musso, Tiziana
Tabbia, Giuseppe
Bardessono, Marco
Pasquali, Christian
Mantovani, Alberto
Sozzani, Silvano
Bosisio, Daniela
author_sort Parola, Carmen
collection PubMed
description OM-85 (Broncho-Vaxom®, Broncho-Munal®, Ommunal®, Paxoral®, Vaxoral®), a product made of the water soluble fractions of 21 inactivated bacterial strain patterns responsible for respiratory tract infections, is used for the prevention of recurrent upper respiratory tract infections and acute exacerbations in chronic obstructive pulmonary disease patients. OM-85 is able to potentiate both innate and adaptive immune responses. However, the molecular mechanisms responsible for OM-85 activation are still largely unknown. Purpose of this study was to investigate the impact of OM-85 stimulation on human dendritic cell functions. We show that OM-85 selectively induced NF-kB and MAPK activation in human DC with no detectable action on the interferon regulatory factor (IRF) pathway. As a consequence, chemokines (i.e. CXCL8, CXCL6, CCL3, CCL20, CCL22) and B-cell activating cytokines (i.e. IL-6, BAFF and IL-10) were strongly upregulated. OM-85 also synergized with the action of classical pro-inflammatory stimuli used at suboptimal concentrations. Peripheral blood mononuclear cells from patients with COPD, a pathological condition often associated with altered PRR expression pattern, fully retained the capability to respond to OM-85. These results provide new insights on the molecular mechanisms of OM-85 activation of the immune response and strengthen the rational for its use in clinical settings.
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spelling pubmed-38754222014-01-02 Selective Activation of Human Dendritic Cells by OM-85 through a NF-kB and MAPK Dependent Pathway Parola, Carmen Salogni, Laura Vaira, Xenia Scutera, Sara Somma, Paolo Salvi, Valentina Musso, Tiziana Tabbia, Giuseppe Bardessono, Marco Pasquali, Christian Mantovani, Alberto Sozzani, Silvano Bosisio, Daniela PLoS One Research Article OM-85 (Broncho-Vaxom®, Broncho-Munal®, Ommunal®, Paxoral®, Vaxoral®), a product made of the water soluble fractions of 21 inactivated bacterial strain patterns responsible for respiratory tract infections, is used for the prevention of recurrent upper respiratory tract infections and acute exacerbations in chronic obstructive pulmonary disease patients. OM-85 is able to potentiate both innate and adaptive immune responses. However, the molecular mechanisms responsible for OM-85 activation are still largely unknown. Purpose of this study was to investigate the impact of OM-85 stimulation on human dendritic cell functions. We show that OM-85 selectively induced NF-kB and MAPK activation in human DC with no detectable action on the interferon regulatory factor (IRF) pathway. As a consequence, chemokines (i.e. CXCL8, CXCL6, CCL3, CCL20, CCL22) and B-cell activating cytokines (i.e. IL-6, BAFF and IL-10) were strongly upregulated. OM-85 also synergized with the action of classical pro-inflammatory stimuli used at suboptimal concentrations. Peripheral blood mononuclear cells from patients with COPD, a pathological condition often associated with altered PRR expression pattern, fully retained the capability to respond to OM-85. These results provide new insights on the molecular mechanisms of OM-85 activation of the immune response and strengthen the rational for its use in clinical settings. Public Library of Science 2013-12-30 /pmc/articles/PMC3875422/ /pubmed/24386121 http://dx.doi.org/10.1371/journal.pone.0082867 Text en © 2013 Parola et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Parola, Carmen
Salogni, Laura
Vaira, Xenia
Scutera, Sara
Somma, Paolo
Salvi, Valentina
Musso, Tiziana
Tabbia, Giuseppe
Bardessono, Marco
Pasquali, Christian
Mantovani, Alberto
Sozzani, Silvano
Bosisio, Daniela
Selective Activation of Human Dendritic Cells by OM-85 through a NF-kB and MAPK Dependent Pathway
title Selective Activation of Human Dendritic Cells by OM-85 through a NF-kB and MAPK Dependent Pathway
title_full Selective Activation of Human Dendritic Cells by OM-85 through a NF-kB and MAPK Dependent Pathway
title_fullStr Selective Activation of Human Dendritic Cells by OM-85 through a NF-kB and MAPK Dependent Pathway
title_full_unstemmed Selective Activation of Human Dendritic Cells by OM-85 through a NF-kB and MAPK Dependent Pathway
title_short Selective Activation of Human Dendritic Cells by OM-85 through a NF-kB and MAPK Dependent Pathway
title_sort selective activation of human dendritic cells by om-85 through a nf-kb and mapk dependent pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875422/
https://www.ncbi.nlm.nih.gov/pubmed/24386121
http://dx.doi.org/10.1371/journal.pone.0082867
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