Grigorescu Andra, Riza Anca-Lelia, Streata Ioana, Netea Mihai G
Human Genomics Laboratory, University of Medicine and Pharmacy of Craiova, Craiova, Romania.
Department of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
Am J Physiol Cell Physiol. 2025 Aug 1;329(2):C456-C470. doi: 10.1152/ajpcell.00153.2025. Epub 2025 Jun 16.
Trained immunity (TRIM) is the process through which the innate immune system undergoes memory-like epigenetic and metabolic reprogramming following an earlier infectious challenge. Trained immunity can be induced, in a similar fashion to microbial structures, by various endogenous compounds: oxidized low-density lipoproteins, lipoprotein(a), glucose and uric acid, and monosodium urate. Lipids, glucose, and protein metabolic dysfunction have the potential to perpetuate a proinflammatory feedback loop through the induction of maladaptive trained immunity programs, as shown in cardiovascular diseases, diabetes, and hyperuricemia. Molecular mechanisms leading to TRIM are susceptible to homeostatic disruptions of advanced age, and maladaptive TRIM may be the link between immune aging and age-associated pathologies. The present review discusses the current knowledge on metabolic pathways in adaptive and maladaptive trained immunity and its deleterious consequences of inappropriate activation during aging. Finally, we discuss how several dietary patterns modulate immunometabolism and influence trained immunity in aging.
训练有素的免疫(TRIM)是指先天免疫系统在早期感染挑战后经历类似记忆的表观遗传和代谢重编程的过程。与微生物结构类似,多种内源性化合物可诱导训练有素的免疫,这些化合物包括:氧化型低密度脂蛋白、脂蛋白(a)、葡萄糖、尿酸和尿酸钠。脂质、葡萄糖和蛋白质代谢功能障碍有可能通过诱导适应不良的训练有素的免疫程序,使促炎反馈回路持续存在,如在心血管疾病、糖尿病和高尿酸血症中所见。导致TRIM的分子机制易受衰老导致的体内平衡破坏的影响,而适应不良的TRIM可能是免疫衰老与年龄相关病理之间的联系。本综述讨论了关于适应性和适应不良的训练有素免疫中的代谢途径的现有知识,以及其在衰老过程中不适当激活的有害后果。最后,我们讨论了几种饮食模式如何调节免疫代谢并影响衰老过程中的训练有素的免疫。