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Lactobacillus rhamnosus GG-Derived Soluble Mediators Modulate Adaptive Immune Cells

Probiotics and probiotic-related nutritional interventions have been described to have beneficial effects on immune homeostasis and gut health. In previous studies, Lactobacillus rhamnosus GG (LGG) soluble mediators (LSM) have been demonstrated to exert beneficial effects in preclinical models of al...

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Autores principales: Ludwig, Irene S., Broere, Femke, Manurung, Sarmauli, Lambers, Tim T., van der Zee, Ruurd, van Eden, Willem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048560/
https://www.ncbi.nlm.nih.gov/pubmed/30042761
http://dx.doi.org/10.3389/fimmu.2018.01546
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author Ludwig, Irene S.
Broere, Femke
Manurung, Sarmauli
Lambers, Tim T.
van der Zee, Ruurd
van Eden, Willem
author_facet Ludwig, Irene S.
Broere, Femke
Manurung, Sarmauli
Lambers, Tim T.
van der Zee, Ruurd
van Eden, Willem
author_sort Ludwig, Irene S.
collection PubMed
description Probiotics and probiotic-related nutritional interventions have been described to have beneficial effects on immune homeostasis and gut health. In previous studies, Lactobacillus rhamnosus GG (LGG) soluble mediators (LSM) have been demonstrated to exert beneficial effects in preclinical models of allergic sensitization, bacterial infection, and intestinal barrier function. In the context of allergic diseases, differentiation of dendritic cells (DCs) and their interactions with T cell populations are crucial for driving tolerogenic responses. In this study, we set out to evaluate whether these LSM can modulate DC maturation and have an impact on prompting protective and/or tolerogenic T cell responses. Monocytes were isolated from PBMC of healthy blood donors and cultured in the presence of GM-CSF, IL-4, and LSM or unconditioned bacterial culture medium control (UCM) during 6 days to induce DC differentiation. Subsequently, these DCs were matured in the presence of TNF-α for 1 day and analyzed for their phenotype and ability to induce autologous T cell activation and differentiation to model recall antigens. After 7 days of co-culture, T cells were analyzed for activation and differentiation by flow cytometry of intracellular cytokines (IFN-γ, IL-2, IL-10, and IL-17A), activation markers (CD25), and Foxp3+ expression. LSM did not alter DC numbers or maturation status. However, these DCs did show improved capacity to induce a T cell response as shown by increased IL-2 and IFN-γ producing T cell populations upon stimulation with recall antigens. These enhanced recall responses coincided with enhanced Foxp3+ expression that was not observed when T cells were cultured in the presence of UCM-treated DCs. By contrast, the number of activated T cells (determined by CD25 expression) was only slightly increased. In conclusion, this study reveals that LSM can influence adaptive immune responses as shown by the modulation of DC functionality. These mechanisms might contribute to previous observed effects in animal models in vivo. Altogether, these results suggest that LSM may provide an alternative to live probiotics in case life bacteria may not be used because of health conditions, although further clinical testing is needed.
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spelling pubmed-60485602018-07-24 Lactobacillus rhamnosus GG-Derived Soluble Mediators Modulate Adaptive Immune Cells Ludwig, Irene S. Broere, Femke Manurung, Sarmauli Lambers, Tim T. van der Zee, Ruurd van Eden, Willem Front Immunol Immunology Probiotics and probiotic-related nutritional interventions have been described to have beneficial effects on immune homeostasis and gut health. In previous studies, Lactobacillus rhamnosus GG (LGG) soluble mediators (LSM) have been demonstrated to exert beneficial effects in preclinical models of allergic sensitization, bacterial infection, and intestinal barrier function. In the context of allergic diseases, differentiation of dendritic cells (DCs) and their interactions with T cell populations are crucial for driving tolerogenic responses. In this study, we set out to evaluate whether these LSM can modulate DC maturation and have an impact on prompting protective and/or tolerogenic T cell responses. Monocytes were isolated from PBMC of healthy blood donors and cultured in the presence of GM-CSF, IL-4, and LSM or unconditioned bacterial culture medium control (UCM) during 6 days to induce DC differentiation. Subsequently, these DCs were matured in the presence of TNF-α for 1 day and analyzed for their phenotype and ability to induce autologous T cell activation and differentiation to model recall antigens. After 7 days of co-culture, T cells were analyzed for activation and differentiation by flow cytometry of intracellular cytokines (IFN-γ, IL-2, IL-10, and IL-17A), activation markers (CD25), and Foxp3+ expression. LSM did not alter DC numbers or maturation status. However, these DCs did show improved capacity to induce a T cell response as shown by increased IL-2 and IFN-γ producing T cell populations upon stimulation with recall antigens. These enhanced recall responses coincided with enhanced Foxp3+ expression that was not observed when T cells were cultured in the presence of UCM-treated DCs. By contrast, the number of activated T cells (determined by CD25 expression) was only slightly increased. In conclusion, this study reveals that LSM can influence adaptive immune responses as shown by the modulation of DC functionality. These mechanisms might contribute to previous observed effects in animal models in vivo. Altogether, these results suggest that LSM may provide an alternative to live probiotics in case life bacteria may not be used because of health conditions, although further clinical testing is needed. Frontiers Media S.A. 2018-07-10 /pmc/articles/PMC6048560/ /pubmed/30042761 http://dx.doi.org/10.3389/fimmu.2018.01546 Text en Copyright © 2018 Ludwig, Broere, Manurung, Lambers, van der Zee and van Eden. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Ludwig, Irene S.
Broere, Femke
Manurung, Sarmauli
Lambers, Tim T.
van der Zee, Ruurd
van Eden, Willem
Lactobacillus rhamnosus GG-Derived Soluble Mediators Modulate Adaptive Immune Cells
title Lactobacillus rhamnosus GG-Derived Soluble Mediators Modulate Adaptive Immune Cells
title_full Lactobacillus rhamnosus GG-Derived Soluble Mediators Modulate Adaptive Immune Cells
title_fullStr Lactobacillus rhamnosus GG-Derived Soluble Mediators Modulate Adaptive Immune Cells
title_full_unstemmed Lactobacillus rhamnosus GG-Derived Soluble Mediators Modulate Adaptive Immune Cells
title_short Lactobacillus rhamnosus GG-Derived Soluble Mediators Modulate Adaptive Immune Cells
title_sort lactobacillus rhamnosus gg-derived soluble mediators modulate adaptive immune cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048560/
https://www.ncbi.nlm.nih.gov/pubmed/30042761
http://dx.doi.org/10.3389/fimmu.2018.01546
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