Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania.
Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania;
J Nucl Med. 2021 Jul 1;62(7):896-902. doi: 10.2967/jnumed.120.245407. Epub 2021 May 7.
Over the past decade, there has been a growing recognition of the links between intracellular metabolism and immune cell activation, that is, immunometabolism, and its consequences in atherogenesis. However, most immunometabolic investigations have been conducted in cultured cells through pharmacologic or genetic manipulations of selected immunologic or metabolic pathways, limiting their extrapolation to the complex microenvironment of plaques. In vivo metabolic imaging is ideally situated to address this gap and to determine the clinical implications of immunometabolic alterations for diagnosis and management of patients. Indeed, F-FDG has been widely used in clinical studies with promising results for risk stratification of atherosclerosis and monitoring the response to therapeutic interventions, though the biologic basis of its uptake in plaques has been evolving. Herein, we describe recent advances in understanding of immunometabolism of atherosclerosis with an emphasis on macrophages, and we review promising metabolic imaging approaches using F-FDG and other PET radiotracers.
在过去的十年中,人们越来越认识到细胞内代谢与免疫细胞激活之间的联系,即免疫代谢,及其在动脉粥样硬化形成中的后果。然而,大多数免疫代谢研究都是通过对选定的免疫或代谢途径进行药理学或遗传操作在培养细胞中进行的,这限制了它们对斑块复杂微环境的推断。体内代谢成像非常适合解决这一差距,并确定免疫代谢改变对诊断和治疗患者的临床意义。事实上,氟代脱氧葡萄糖(F-FDG)已广泛应用于临床研究,其在动脉粥样硬化风险分层和监测治疗干预反应方面的结果令人鼓舞,尽管其在斑块中的摄取的生物学基础一直在发展。在此,我们描述了对动脉粥样硬化免疫代谢的理解的最新进展,重点是巨噬细胞,并综述了使用 F-FDG 和其他正电子发射断层扫描(PET)放射性示踪剂的有前途的代谢成像方法。