Laboratorio di Immunologia, Istituto per l'Endocrinologia e l'Oncologia Sperimentale "G. Salvatore," Consiglio Nazionale delle Ricerche, Napoli, Italy.
Unità di Neuroimmunologia, IRCCS-Fondazione Santa Lucia, Roma, Italy.
J Immunol. 2024 Jun 15;212(12):1859-1866. doi: 10.4049/jimmunol.2400079.
Immunometabolism has been demonstrated to control immune tolerance and the pathogenic events leading to autoimmunity. Compelling experimental evidence also suggests that intracellular metabolic programs influence differentiation, phenotype, proliferation, and effector functions of anti-inflammatory CD4+CD25+Foxp3+ regulatory T (Treg) cells. Indeed, alterations in intracellular metabolism associate with quantitative and qualitative impairments of Treg cells in several pathological conditions. In this review, we summarize the most recent advances linking how metabolic pathways control Treg cell homeostasis and their alterations occurring in autoimmunity. Also, we analyze how metabolic manipulations could be employed to restore Treg cell frequency and function with the aim to create novel therapeutic opportunities to halt immune-mediated disorders.
免疫代谢已被证明可以控制免疫耐受和导致自身免疫的发病事件。令人信服的实验证据还表明,细胞内代谢程序会影响抗炎性 CD4+CD25+Foxp3+调节性 T(Treg)细胞的分化、表型、增殖和效应功能。事实上,在几种病理情况下,细胞内代谢的改变与 Treg 细胞的定量和定性损伤有关。在这篇综述中,我们总结了将代谢途径如何控制 Treg 细胞动态平衡及其在自身免疫中发生改变的最新进展。此外,我们还分析了代谢操作如何被用来恢复 Treg 细胞的频率和功能,以期为阻止免疫介导的疾病创造新的治疗机会。