Institute of Pharmacology and Experimental Therapeutics, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Coimbra Institute for Clinical and Biomedical Research (iCBR), Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Front Immunol. 2024 Mar 15;15:1360065. doi: 10.3389/fimmu.2024.1360065. eCollection 2024.
Mounting evidence progressively appreciates the vital interplay between immunity and metabolism in a wide array of immunometabolic chronic disorders, both autoimmune and non-autoimmune mediated. The immune system regulates the functioning of cellular metabolism within organs like the brain, pancreas and/or adipose tissue by sensing and adapting to fluctuations in the microenvironment's nutrients, thereby reshaping metabolic pathways that greatly impact a pro- or anti-inflammatory immunophenotype. While it is agreed that the immune system relies on an adequate nutritional status to function properly, we are only just starting to understand how the supply of single or combined nutrients, all of them termed immunonutrients, can steer immune cells towards a less inflamed, tolerogenic immunophenotype. Polyphenols, a class of secondary metabolites abundant in Mediterranean foods, are pharmacologically active natural products with outstanding immunomodulatory actions. Upon binding to a range of receptors highly expressed in immune cells (e.g. AhR, RAR, RLR), they act in immunometabolic pathways through a mitochondria-centered multi-modal approach. , polyphenols activate nutrient sensing via stress-response pathways, essential for immune responses. , they regulate mammalian target of rapamycin (mTOR)/AMP-activated protein kinase (AMPK) balance in immune cells and are well-tolerated caloric restriction mimetics. , polyphenols interfere with the assembly of NLR family pyrin domain containing 3 (NLRP3) in endoplasmic reticulum-mitochondria contact sites, inhibiting its activation while improving mitochondrial biogenesis and autophagosome-lysosome fusion. , polyphenols impact chromatin remodeling and coordinates both epigenetic and metabolic reprogramming. This work moves beyond the well-documented antioxidant properties of polyphenols, offering new insights into the multifaceted nature of these compounds. It proposes a mechanistical appraisal on the regulatory pathways through which polyphenols modulate the immune response, thereby alleviating chronic low-grade inflammation. Furthermore, it draws parallels between pharmacological interventions and polyphenol-based immunonutrition in their modes of immunomodulation across a wide spectrum of socioeconomically impactful immunometabolic diseases such as Multiple Sclerosis, Diabetes (type 1 and 2) or even Alzheimer's disease. Lastly, it discusses the existing challenges that thwart the translation of polyphenols-based immunonutritional interventions into long-term clinical studies. Overcoming these limitations will undoubtedly pave the way for improving precision nutrition protocols and provide personalized guidance on tailored polyphenol-based immunonutrition plans.
越来越多的证据表明,在广泛的免疫代谢慢性疾病中,包括自身免疫和非自身免疫介导的疾病,免疫和代谢之间存在着至关重要的相互作用。免疫系统通过感知和适应微环境中营养物质的波动来调节大脑、胰腺和/或脂肪组织等器官中细胞代谢的功能,从而重塑代谢途径,极大地影响促炎或抗炎免疫表型。虽然人们已经认识到免疫系统依赖于充足的营养状态来正常运作,但我们才刚刚开始了解单一或组合营养素(统称为免疫营养素)的供应如何使免疫细胞向炎症程度较低、耐受性更强的免疫表型转变。多酚是一类在地中海食物中含量丰富的次生代谢物,是具有出色免疫调节作用的药理活性天然产物。多酚通过与免疫细胞中高度表达的一系列受体(如 AhR、RAR、RLR)结合,通过以线粒体为中心的多模式途径作用于免疫代谢途径。一方面,多酚通过应激反应途径激活营养感应,这对免疫反应至关重要。另一方面,它们调节免疫细胞中的哺乳动物雷帕霉素靶蛋白(mTOR)/AMP 激活蛋白激酶(AMPK)平衡,并且是耐受良好的热量限制模拟物。此外,多酚干扰内质网-线粒体接触部位富含 N 端亮氨酸重复域 3(NLRP3)的 NLR 家族吡啶结构域的组装,抑制其激活,同时改善线粒体生物发生和自噬体-溶酶体融合。最后,多酚影响染色质重塑,并协调表观遗传和代谢重编程。这项工作超越了多酚众所周知的抗氧化特性,为这些化合物的多面性提供了新的见解。它提出了一种关于多酚调节免疫反应的调节途径的机制评估,从而缓解慢性低度炎症。此外,它在广泛的具有社会经济影响的免疫代谢疾病(如多发性硬化症、1 型和 2 型糖尿病甚至阿尔茨海默病)中,比较了药理学干预和基于多酚的免疫营养在免疫调节模式方面的相似之处。最后,它讨论了阻碍多酚基免疫营养干预转化为长期临床研究的现有挑战。克服这些限制无疑将为改善精准营养方案铺平道路,并提供基于定制多酚的免疫营养计划的个性化指导。