Ontology highlight
ABSTRACT: 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.
SUBMITTER: Santiago KB
PROVIDER: S-EPMC9851646 | biostudies-literature | 2023
REPOSITORIES: biostudies-literature
Santiago Karina Basso KB Conti Bruno José BJ Cardoso Eliza de Oliveira EO Conte Fernanda Lopes FL Tasca Karen Ingrid KI Romagnoli Graziela Gorete GG Golim Marjorie de Assis MA Cruz Maria Tereza MT Sforcin José Maurício JM
The journal of venomous animals and toxins including tropical diseases 20230113
<h4>Background</h4>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.<h4>Methods</h4>Cell viability, lymphocyte proliferation, gene expression (T-bet and FoxP3), and cytokine production by DCs (TNF-α, IL-10, IL-6 an ...[more]