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The potential immunomodulatory role of the gut microbiota in the pathogenesis of asthma: an in vitro study
The aim of this study was to investigate the influence of Bacteroides vulgatus (BV), Clostridium perfringens (CP), Parabacteroides distasonis (PD) and Ruminococcus albus (RA) lysates on secretion of selected cytokines by PBMC, MDM and HT-29 cells, as well as to determine the potential mechanisms of...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643691/ https://www.ncbi.nlm.nih.gov/pubmed/37957277 http://dx.doi.org/10.1038/s41598-023-47003-0 |
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author | Kleniewska, Paulina Kopa-Stojak, Paulina Natalia Hoffmann, Arkadiusz Pawliczak, Rafał |
author_facet | Kleniewska, Paulina Kopa-Stojak, Paulina Natalia Hoffmann, Arkadiusz Pawliczak, Rafał |
author_sort | Kleniewska, Paulina |
collection | PubMed |
description | The aim of this study was to investigate the influence of Bacteroides vulgatus (BV), Clostridium perfringens (CP), Parabacteroides distasonis (PD) and Ruminococcus albus (RA) lysates on secretion of selected cytokines by PBMC, MDM and HT-29 cells, as well as to determine the potential mechanisms of their action in the development of asthma. Enzyme-linked immunosorbent assays were used to analyze the effect of BV, CP, PD and RA lysates on the secretion of IL-1β, IL-6, IL-10 and TNF-α by human PBMC, MDM and HT-29 cells. BV and CP lysates significantly lowered IL-1β secretion by MDM vs. control (p < 0.05 and p < 0.001 respectively) but only at a dose of 400 µg lysate. The secretions of IL-6 by PBMC and MDM were elevated significantly above control values (p < 0.05) after administration of CP and PD lysates. BV, CP and PD lysates (100 µg) significantly increased IL-10 secretion by PBMC vs. control (p < 0.05). CP, PD and RA lysates (400 µg) significantly increased IL-10 secretion by MDM vs. control (p < 0.001). BV lysate (400 µg) also significantly increased IL-10 secretion by MDM as compared to control (p < 0.05). In PBMC and MDM, the production levels of the anti-inflammatory cytokine were increased by all the bacterial lysates used in a dose-dependent manner. |
format | Online Article Text |
id | pubmed-10643691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106436912023-11-13 The potential immunomodulatory role of the gut microbiota in the pathogenesis of asthma: an in vitro study Kleniewska, Paulina Kopa-Stojak, Paulina Natalia Hoffmann, Arkadiusz Pawliczak, Rafał Sci Rep Article The aim of this study was to investigate the influence of Bacteroides vulgatus (BV), Clostridium perfringens (CP), Parabacteroides distasonis (PD) and Ruminococcus albus (RA) lysates on secretion of selected cytokines by PBMC, MDM and HT-29 cells, as well as to determine the potential mechanisms of their action in the development of asthma. Enzyme-linked immunosorbent assays were used to analyze the effect of BV, CP, PD and RA lysates on the secretion of IL-1β, IL-6, IL-10 and TNF-α by human PBMC, MDM and HT-29 cells. BV and CP lysates significantly lowered IL-1β secretion by MDM vs. control (p < 0.05 and p < 0.001 respectively) but only at a dose of 400 µg lysate. The secretions of IL-6 by PBMC and MDM were elevated significantly above control values (p < 0.05) after administration of CP and PD lysates. BV, CP and PD lysates (100 µg) significantly increased IL-10 secretion by PBMC vs. control (p < 0.05). CP, PD and RA lysates (400 µg) significantly increased IL-10 secretion by MDM vs. control (p < 0.001). BV lysate (400 µg) also significantly increased IL-10 secretion by MDM as compared to control (p < 0.05). In PBMC and MDM, the production levels of the anti-inflammatory cytokine were increased by all the bacterial lysates used in a dose-dependent manner. Nature Publishing Group UK 2023-11-13 /pmc/articles/PMC10643691/ /pubmed/37957277 http://dx.doi.org/10.1038/s41598-023-47003-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 | Article Kleniewska, Paulina Kopa-Stojak, Paulina Natalia Hoffmann, Arkadiusz Pawliczak, Rafał The potential immunomodulatory role of the gut microbiota in the pathogenesis of asthma: an in vitro study |
title | The potential immunomodulatory role of the gut microbiota in the pathogenesis of asthma: an in vitro study |
title_full | The potential immunomodulatory role of the gut microbiota in the pathogenesis of asthma: an in vitro study |
title_fullStr | The potential immunomodulatory role of the gut microbiota in the pathogenesis of asthma: an in vitro study |
title_full_unstemmed | The potential immunomodulatory role of the gut microbiota in the pathogenesis of asthma: an in vitro study |
title_short | The potential immunomodulatory role of the gut microbiota in the pathogenesis of asthma: an in vitro study |
title_sort | potential immunomodulatory role of the gut microbiota in the pathogenesis of asthma: an in vitro study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643691/ https://www.ncbi.nlm.nih.gov/pubmed/37957277 http://dx.doi.org/10.1038/s41598-023-47003-0 |
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