Fernandes Iara Grigoletto, Oliveira Luana de M, Andrade Milena M de Souza, Alberca Ricardo W, Lima Júlia Cataldo, de Sousa Emanuella Sarmento Alho, Pietrobon Anna Julia, Pereira Nátalli Zanete, Castelo Branco Anna Cláudia Calvielli, Duarte Alberto José da Silva, Sato Maria Notomi
Laboratory of Dermatology and Immunodeficiencies, LIM-56, Tropical Medicine Institute of Sao Paulo, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo 05508-000, Brazil.
Department of Dermatology, Laboratory of Dermatology and Immunodeficiencies, LIM-56, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo 05508-000, Brazil.
Int J Mol Sci. 2025 Mar 6;26(5):2345. doi: 10.3390/ijms26052345.
Immunosenescence, a process with a dysfunctional immune response that may favor infection is associated with an increase in inflammatory responses mediated by proinflammatory cytokines, characteristic of inflammaging. Aging and immunosenescence have a relationship relating to oxidative stress and inflammaging. Therefore, natural antioxidant compounds could be candidates for the control of the oxidative process. Our purpose was to evaluate the effect of resveratrol (Resv) on the antioxidant, antiviral, and anti-inflammatory responses induced by toll-like receptors (TLRs) 3, 4, and 7/8 agonists stimulation on peripheral blood mononuclear cells (PBMCs) of elderly and healthy female individuals (63-82 years old) and young and healthy female individuals (21-31 years old). Our data show that Resv may upregulate antioxidant factor expression, such as catalase (CAT) and SIRT1, in response to TLR4 and TLR7/8 agonists, similarly in both young and aged groups. Moreover, the Resv anti-inflammatory effect was detected by inhibiting IL-1β, TNF-α, and IL-10 secretion levels, as well as by the chemokines CCL2 and CCL5, induced by TLR4 and TLR7/8 stimulation. Curiously, Resv decreased antiviral genes, such as MxA, STING, and IRF7 expression, possibly by reducing the inflammatory effects of interferon-induced genes. Taken together, our results demonstrate the ability of Resv to stimulate antioxidant factors, leading to a downmodulation of the inflammatory response induced by innate immune stimulation. These findings point out Resv as a strategy to control the upregulation of inflammatory response, even in elderly individuals.
免疫衰老,是一个免疫反应功能失调且可能易引发感染的过程,与促炎细胞因子介导的炎症反应增加相关,这是炎症衰老的特征。衰老与免疫衰老和氧化应激以及炎症衰老存在关联。因此,天然抗氧化化合物可能是控制氧化过程的候选物质。我们的目的是评估白藜芦醇(Resv)对老年(63 - 82岁)和年轻(21 - 31岁)健康女性外周血单个核细胞(PBMCs)中Toll样受体(TLRs)3、4和7/8激动剂刺激所诱导的抗氧化、抗病毒和抗炎反应的影响。我们的数据表明,Resv可能上调抗氧化因子的表达,如过氧化氢酶(CAT)和SIRT1,以响应TLR4和TLR7/8激动剂,在年轻组和老年组中情况相似。此外,通过抑制TLR4和TLR7/8刺激诱导的IL - 1β、TNF - α和IL - 10的分泌水平以及趋化因子CCL2和CCL5,检测到了Resv的抗炎作用。奇怪的是,Resv可能通过降低干扰素诱导基因的炎症效应,降低了抗病毒基因如Mx A、STING和IRF7的表达。综上所述,我们的结果证明了Resv刺激抗氧化因子的能力,导致先天免疫刺激所诱导的炎症反应下调。这些发现指出Resv是一种控制炎症反应上调的策略,即使在老年人中也是如此。