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Effects of probiotics on the enhancement of the innate mucosal immune response against pathogenic bacteria

BACKGROUND AND OBJECTIVES: Probiotics have been widely used for host immune system enhancement but with limited knowledge regarding the immunomodulation mechanisms by which they assist the mucosal innate immune response. We investigated the effects of probiotics on the modulation of the innate mucos...

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Autores principales: Darma, Andy, Athiyyah, Alpha Fardah, Ranuh, Reza Gunadi, Endaryanto, Anang, Budiono, Budiono, Sudarmo, Subijanto Marto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867706/
https://www.ncbi.nlm.nih.gov/pubmed/33604000
http://dx.doi.org/10.18502/ijm.v12i5.4606
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author Darma, Andy
Athiyyah, Alpha Fardah
Ranuh, Reza Gunadi
Endaryanto, Anang
Budiono, Budiono
Sudarmo, Subijanto Marto
author_facet Darma, Andy
Athiyyah, Alpha Fardah
Ranuh, Reza Gunadi
Endaryanto, Anang
Budiono, Budiono
Sudarmo, Subijanto Marto
author_sort Darma, Andy
collection PubMed
description BACKGROUND AND OBJECTIVES: Probiotics have been widely used for host immune system enhancement but with limited knowledge regarding the immunomodulation mechanisms by which they assist the mucosal innate immune response. We investigated the effects of probiotics on the modulation of the innate mucosal immune response particularly in association with Toll-like receptor (TLR)-2, TLR-4 and nuclear factor-kappa B (NF-κB) p65 and p105. MATERIALS AND METHODS: We randomized 24 male BALB/c mice into four groups. Two groups were administered probiotics for 21 consecutive days; one of these groups was challenged with Lipopolysaccharide (LPS) on day 15. The third group was challenged with only LPS. The fourth group remained untreated. All mice were sacrificed after 21 days. An immunohistochemistry procedure on the ileum was performed and monoclonal antibodies specific for TLR-2, TLR-4 and NF-κB p65 and p105 were used for the analysis of innate lymphoid cells. RESULTS: In the LPS-only treated group, there was a significant decrease in p105, indicating an alternative transcription pathway for the process of pro-inflammatory cytokine production. In the probiotics-only treated group there was significant enhancement of TLR-2 and TLR-4 and NF-κB p65 and p105. When mice treated with probiotics were exposed to LPS, there was a significant decrease in NF-κB p65 and p105, indicating employment of the classical pathway for pro-inflammatory cytokine production. CONCLUSION: Probiotics can enhance the innate mucosal immune response in healthy mice and can maintain the homeostasis of the gut mucosal immune response against LPS through the activation of the classical NF-κB pathway.
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spelling pubmed-78677062021-02-17 Effects of probiotics on the enhancement of the innate mucosal immune response against pathogenic bacteria Darma, Andy Athiyyah, Alpha Fardah Ranuh, Reza Gunadi Endaryanto, Anang Budiono, Budiono Sudarmo, Subijanto Marto Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: Probiotics have been widely used for host immune system enhancement but with limited knowledge regarding the immunomodulation mechanisms by which they assist the mucosal innate immune response. We investigated the effects of probiotics on the modulation of the innate mucosal immune response particularly in association with Toll-like receptor (TLR)-2, TLR-4 and nuclear factor-kappa B (NF-κB) p65 and p105. MATERIALS AND METHODS: We randomized 24 male BALB/c mice into four groups. Two groups were administered probiotics for 21 consecutive days; one of these groups was challenged with Lipopolysaccharide (LPS) on day 15. The third group was challenged with only LPS. The fourth group remained untreated. All mice were sacrificed after 21 days. An immunohistochemistry procedure on the ileum was performed and monoclonal antibodies specific for TLR-2, TLR-4 and NF-κB p65 and p105 were used for the analysis of innate lymphoid cells. RESULTS: In the LPS-only treated group, there was a significant decrease in p105, indicating an alternative transcription pathway for the process of pro-inflammatory cytokine production. In the probiotics-only treated group there was significant enhancement of TLR-2 and TLR-4 and NF-κB p65 and p105. When mice treated with probiotics were exposed to LPS, there was a significant decrease in NF-κB p65 and p105, indicating employment of the classical pathway for pro-inflammatory cytokine production. CONCLUSION: Probiotics can enhance the innate mucosal immune response in healthy mice and can maintain the homeostasis of the gut mucosal immune response against LPS through the activation of the classical NF-κB pathway. Tehran University of Medical Sciences 2020-10 /pmc/articles/PMC7867706/ /pubmed/33604000 http://dx.doi.org/10.18502/ijm.v12i5.4606 Text en Copyright© 2020 The Authors. This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license, (https://creativecommons.org/licenses/by-nc/4.0/) Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Article
Darma, Andy
Athiyyah, Alpha Fardah
Ranuh, Reza Gunadi
Endaryanto, Anang
Budiono, Budiono
Sudarmo, Subijanto Marto
Effects of probiotics on the enhancement of the innate mucosal immune response against pathogenic bacteria
title Effects of probiotics on the enhancement of the innate mucosal immune response against pathogenic bacteria
title_full Effects of probiotics on the enhancement of the innate mucosal immune response against pathogenic bacteria
title_fullStr Effects of probiotics on the enhancement of the innate mucosal immune response against pathogenic bacteria
title_full_unstemmed Effects of probiotics on the enhancement of the innate mucosal immune response against pathogenic bacteria
title_short Effects of probiotics on the enhancement of the innate mucosal immune response against pathogenic bacteria
title_sort effects of probiotics on the enhancement of the innate mucosal immune response against pathogenic bacteria
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867706/
https://www.ncbi.nlm.nih.gov/pubmed/33604000
http://dx.doi.org/10.18502/ijm.v12i5.4606
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