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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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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. |
format | Online Article Text |
id | pubmed-3875422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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