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Hum Immunol ; 84(9): 471-483, 2023 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-37331910

RESUMO

AIMS: A hyperinflammatory condition is brought on by the development of Coronavirus disease 2019 (COVID-19), which is characterized by an elevation of T helper (Th) 17 cells, high levels of pro-inflammatory cytokines, and a depletion of regulatory T (Treg) cells. METHODS: In this research, we examined the effect of nano-curcumin and catechin on the TCD4+, TCD8+, Th17, and Treg cells and their associated factors in COVID-19 patients. For this purpose, 160 (50 patients excluded during the study) COVID-19 patients were divided into four groups: placebo, nano-curcumin, catechin, and nano-curcumin + catechin. The frequency of TCD4+, TCD8+, Th17, and Treg cells, the gene expression of transcription factors (STAT3, RORt, and FoxP3) relevant to Th17 and Treg, as well as the serum levels of cytokines (IL-6, IL17, IL1-b, IL-10, and TGF-), were all evaluated intra- and inter-group, before and after treatment, in all groups. RESULTS: Our study showed that TCD4 + and TCD8 + cells were significantly higher in the nano-curcumin + catechin group compared to the control group, whereas Th17 was lower than the initial value. Furthermore, compared to the placebo-received group, cytokines and transcription factors associated with Th17 were significantly lower in the nano-curcumin + catechin group. Additionally, combined therapy increased Treg cells and transcription factors compared to the placebo group. CONCLUSION: Overall, our results show that combining nano-curcumin with catechin has a more notable impact on the enhancement of TCD4+, TCD8+, and Treg cells, as well as a decrease in Th17 cells and their mediators, suggesting a promising combination therapy in reducing the inflammatory conditions of COVID-19 infected patients.


Assuntos
COVID-19 , Catequina , Curcumina , Humanos , COVID-19/metabolismo , Curcumina/uso terapêutico , Curcumina/metabolismo , Curcumina/farmacologia , Catequina/uso terapêutico , Catequina/metabolismo , Catequina/farmacologia , Citocinas/metabolismo , Linfócitos T Reguladores/metabolismo , Células Th17/metabolismo , Fatores de Transcrição/metabolismo , Fatores de Transcrição/farmacologia
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