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Immune Response to Bifidobacterium bifidum Strains Support Treg/Th17 Plasticity
In this work we analyzed the immune activation properties of different Bifidobacterium strains in order to establish their ability as inductors of specific effector (Th) or regulatory (Treg) responses. First, we determined the cytokine pattern induced by 21 Bifidobacterium strains in peripheral bloo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178565/ https://www.ncbi.nlm.nih.gov/pubmed/21966367 http://dx.doi.org/10.1371/journal.pone.0024776 |
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author | López, Patricia González-Rodríguez, Irene Gueimonde, Miguel Margolles, Abelardo Suárez, Ana |
author_facet | López, Patricia González-Rodríguez, Irene Gueimonde, Miguel Margolles, Abelardo Suárez, Ana |
author_sort | López, Patricia |
collection | PubMed |
description | In this work we analyzed the immune activation properties of different Bifidobacterium strains in order to establish their ability as inductors of specific effector (Th) or regulatory (Treg) responses. First, we determined the cytokine pattern induced by 21 Bifidobacterium strains in peripheral blood mononuclear cells (PBMCs). Results showed that four Bifidobacterium bifidum strains showed the highest production of IL-17 as well as a poor secretion of IFNγ and TNFα, suggesting a Th17 profile whereas other Bifidobacterium strains exhibited a Th1-suggestive profile. Given the key role of Th17 subsets in mucosal defence, strains suggestive of Th17 responses and the putative Th1 Bifidobacterium breve BM12/11 were selected to stimulate dendritic cells (DC) to further determine their capability to induce the differentiation of naïve CD4(+) lymphocytes toward different Th or Treg cells. All selected strains were able to induce phenotypic DC maturation, but showed differences in cytokine stimulation, DC treated with the putative Th17 strains displaying high IL-1β/IL-12 and low IL-12/IL-10 index, whereas BM12/11-DC exhibited the highest IL-12/IL-10 ratio. Differentiation of naïve lymphocytes confirmed Th1 polarization by BM12/11. Unexpectedly, any B. bifidum strain showed significant capability for Th17 generation, and they were able to generate functional Treg, thus suggesting differences between in vivo and vitro responses. In fact, activation of memory lymphocytes present in PBMCS with these bacteria, point out the presence in vivo of specific Th17 cells, supporting the plasticity of Treg/Th17 populations and the key role of commensal bacteria in mucosal tolerance and T cell reprogramming when needed. |
format | Online Article Text |
id | pubmed-3178565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31785652011-09-30 Immune Response to Bifidobacterium bifidum Strains Support Treg/Th17 Plasticity López, Patricia González-Rodríguez, Irene Gueimonde, Miguel Margolles, Abelardo Suárez, Ana PLoS One Research Article In this work we analyzed the immune activation properties of different Bifidobacterium strains in order to establish their ability as inductors of specific effector (Th) or regulatory (Treg) responses. First, we determined the cytokine pattern induced by 21 Bifidobacterium strains in peripheral blood mononuclear cells (PBMCs). Results showed that four Bifidobacterium bifidum strains showed the highest production of IL-17 as well as a poor secretion of IFNγ and TNFα, suggesting a Th17 profile whereas other Bifidobacterium strains exhibited a Th1-suggestive profile. Given the key role of Th17 subsets in mucosal defence, strains suggestive of Th17 responses and the putative Th1 Bifidobacterium breve BM12/11 were selected to stimulate dendritic cells (DC) to further determine their capability to induce the differentiation of naïve CD4(+) lymphocytes toward different Th or Treg cells. All selected strains were able to induce phenotypic DC maturation, but showed differences in cytokine stimulation, DC treated with the putative Th17 strains displaying high IL-1β/IL-12 and low IL-12/IL-10 index, whereas BM12/11-DC exhibited the highest IL-12/IL-10 ratio. Differentiation of naïve lymphocytes confirmed Th1 polarization by BM12/11. Unexpectedly, any B. bifidum strain showed significant capability for Th17 generation, and they were able to generate functional Treg, thus suggesting differences between in vivo and vitro responses. In fact, activation of memory lymphocytes present in PBMCS with these bacteria, point out the presence in vivo of specific Th17 cells, supporting the plasticity of Treg/Th17 populations and the key role of commensal bacteria in mucosal tolerance and T cell reprogramming when needed. Public Library of Science 2011-09-22 /pmc/articles/PMC3178565/ /pubmed/21966367 http://dx.doi.org/10.1371/journal.pone.0024776 Text en López 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 López, Patricia González-Rodríguez, Irene Gueimonde, Miguel Margolles, Abelardo Suárez, Ana Immune Response to Bifidobacterium bifidum Strains Support Treg/Th17 Plasticity |
title | Immune Response to Bifidobacterium bifidum Strains Support Treg/Th17 Plasticity |
title_full | Immune Response to Bifidobacterium bifidum Strains Support Treg/Th17 Plasticity |
title_fullStr | Immune Response to Bifidobacterium bifidum Strains Support Treg/Th17 Plasticity |
title_full_unstemmed | Immune Response to Bifidobacterium bifidum Strains Support Treg/Th17 Plasticity |
title_short | Immune Response to Bifidobacterium bifidum Strains Support Treg/Th17 Plasticity |
title_sort | immune response to bifidobacterium bifidum strains support treg/th17 plasticity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178565/ https://www.ncbi.nlm.nih.gov/pubmed/21966367 http://dx.doi.org/10.1371/journal.pone.0024776 |
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