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Propolis anti-inflammatory effects on MAGE-1 and retinoic acid-treated dendritic cells and on Th1 and T regulatory cells

BACKGROUND: Propolis exhibits huge potential in the pharmaceutical industry. In the present study, its effects were investigated on dendritic cells (DCs) stimulated with a tumor antigen (MAGE-1) and retinoic acid (RA) and on T lymphocytes to observe a possible differential activation of T lymphocyte...

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Autores principales: Santiago, Karina Basso, Conti, Bruno José, Cardoso, Eliza de Oliveira, Conte, Fernanda Lopes, Tasca, Karen Ingrid, Romagnoli, Graziela Gorete, Golim, Marjorie de Assis, Cruz, Maria Tereza, Sforcin, José Maurício
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP) 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851646/
https://www.ncbi.nlm.nih.gov/pubmed/36721426
http://dx.doi.org/10.1590/1678-9199-JVATITD-2022-0044
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author Santiago, Karina Basso
Conti, Bruno José
Cardoso, Eliza de Oliveira
Conte, Fernanda Lopes
Tasca, Karen Ingrid
Romagnoli, Graziela Gorete
Golim, Marjorie de Assis
Cruz, Maria Tereza
Sforcin, José Maurício
author_facet Santiago, Karina Basso
Conti, Bruno José
Cardoso, Eliza de Oliveira
Conte, Fernanda Lopes
Tasca, Karen Ingrid
Romagnoli, Graziela Gorete
Golim, Marjorie de Assis
Cruz, Maria Tereza
Sforcin, José Maurício
author_sort Santiago, Karina Basso
collection PubMed
description BACKGROUND: Propolis exhibits huge potential in the pharmaceutical industry. In the present study, its effects were investigated on dendritic cells (DCs) stimulated with a tumor antigen (MAGE-1) and retinoic acid (RA) and on T lymphocytes to observe a possible differential activation of T lymphocytes, driving preferentially to Th1 or Treg cells. METHODS: Cell viability, lymphocyte proliferation, gene expression (T-bet and FoxP3), and cytokine production by DCs (TNF-α, IL-10, IL-6 and IL-1β) and lymphocytes (IFN-γ and TGF-β) were analyzed. RESULTS: MAGE-1 and RA alone or in combination with propolis inhibited TNF-α production and induced a higher lymphoproliferation compared to control, while MAGE-1 + propolis induced IL-6 production. Propolis in combination with RA induced FoxP3 expression. MAGE-1 induced IFN-γ production while propolis inhibited it, returning to basal levels. RA inhibited TGF-β production, what was counteracted by propolis. CONCLUSION: Propolis affected immunological parameters inhibiting pro-inflammatory cytokines and favoring the regulatory profile, opening perspectives for the control of inflammatory conditions.
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spelling pubmed-98516462023-01-30 Propolis anti-inflammatory effects on MAGE-1 and retinoic acid-treated dendritic cells and on Th1 and T regulatory cells Santiago, Karina Basso Conti, Bruno José Cardoso, Eliza de Oliveira Conte, Fernanda Lopes Tasca, Karen Ingrid Romagnoli, Graziela Gorete Golim, Marjorie de Assis Cruz, Maria Tereza Sforcin, José Maurício J Venom Anim Toxins Incl Trop Dis Research BACKGROUND: Propolis exhibits huge potential in the pharmaceutical industry. In the present study, its effects were investigated on dendritic cells (DCs) stimulated with a tumor antigen (MAGE-1) and retinoic acid (RA) and on T lymphocytes to observe a possible differential activation of T lymphocytes, driving preferentially to Th1 or Treg cells. METHODS: Cell viability, lymphocyte proliferation, gene expression (T-bet and FoxP3), and cytokine production by DCs (TNF-α, IL-10, IL-6 and IL-1β) and lymphocytes (IFN-γ and TGF-β) were analyzed. RESULTS: MAGE-1 and RA alone or in combination with propolis inhibited TNF-α production and induced a higher lymphoproliferation compared to control, while MAGE-1 + propolis induced IL-6 production. Propolis in combination with RA induced FoxP3 expression. MAGE-1 induced IFN-γ production while propolis inhibited it, returning to basal levels. RA inhibited TGF-β production, what was counteracted by propolis. CONCLUSION: Propolis affected immunological parameters inhibiting pro-inflammatory cytokines and favoring the regulatory profile, opening perspectives for the control of inflammatory conditions. Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP) 2023-01-13 /pmc/articles/PMC9851646/ /pubmed/36721426 http://dx.doi.org/10.1590/1678-9199-JVATITD-2022-0044 Text en https://creativecommons.org/licenses/by/4.0/© The Author(s). 2022 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (https://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Santiago, Karina Basso
Conti, Bruno José
Cardoso, Eliza de Oliveira
Conte, Fernanda Lopes
Tasca, Karen Ingrid
Romagnoli, Graziela Gorete
Golim, Marjorie de Assis
Cruz, Maria Tereza
Sforcin, José Maurício
Propolis anti-inflammatory effects on MAGE-1 and retinoic acid-treated dendritic cells and on Th1 and T regulatory cells
title Propolis anti-inflammatory effects on MAGE-1 and retinoic acid-treated dendritic cells and on Th1 and T regulatory cells
title_full Propolis anti-inflammatory effects on MAGE-1 and retinoic acid-treated dendritic cells and on Th1 and T regulatory cells
title_fullStr Propolis anti-inflammatory effects on MAGE-1 and retinoic acid-treated dendritic cells and on Th1 and T regulatory cells
title_full_unstemmed Propolis anti-inflammatory effects on MAGE-1 and retinoic acid-treated dendritic cells and on Th1 and T regulatory cells
title_short Propolis anti-inflammatory effects on MAGE-1 and retinoic acid-treated dendritic cells and on Th1 and T regulatory cells
title_sort propolis anti-inflammatory effects on mage-1 and retinoic acid-treated dendritic cells and on th1 and t regulatory cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851646/
https://www.ncbi.nlm.nih.gov/pubmed/36721426
http://dx.doi.org/10.1590/1678-9199-JVATITD-2022-0044
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