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Propolis anti-inflammatory effects on MAGE-1 and retinoic acid-treated dendritic cells and on Th1 and T regulatory cells
被引:0
|作者:
Santiago, Karina Basso
[1
]
Conti, Bruno Jose
[1
]
Cardoso, Eliza de Oliveira
[1
]
Conte, Fernanda Lopes
[1
]
Tasca, Karen Ingrid
[1
]
Romagnoli, Graziela Gorete
[1
]
Golim, Marjorie de Assis
[2
]
Cruz, Maria Tereza
[3
]
Sforcin, Jose Mauricio
[1
]
机构:
[1] Sao Paulo State Univ UNESP, Inst Biosci, Botucatu, SP, Brazil
[2] Sao Paulo State Univ UNESP, Sch Med FMB, Botucatu, SP, Brazil
[3] Univ Coimbra, Fac Pharm, Ctr Neurosci & Cellular Biol, Coimbra, Portugal
基金:
巴西圣保罗研究基金会;
关键词:
Dendritic cells;
T CD4+cells;
MAGE-1;
Retinoic acid;
Propolis;
Immunomodulation;
P-COUMARIC ACID;
CYTOKINE PRODUCTION;
IMMUNOMODULATORY ACTIVITY;
BIOLOGICAL-PROPERTIES;
CHEMICAL-COMPOSITION;
ANTIGEN-PRESENTATION;
GREEN PROPOLIS;
EXPRESSION;
ACTIVATION;
IMMUNITY;
D O I:
10.1590/1678-9199-JVATITD-2022-0044
中图分类号:
R99 [毒物学(毒理学)];
学科分类号:
100405 ;
摘要:
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-alpha, IL-10, IL-6 and IL-1 beta) and lymphocytes (IFN-gamma and TGF-beta) were analyzed.Results: MAGE-1 and RA alone or in combination with propolis inhibited TNF-alpha 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-gamma production while propolis inhibited it, returning to basal levels. RA inhibited TGF-beta 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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页数:12
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