Department of Medical Biochemistry, Amsterdam Cardiovascular Sciences (ACS), Amsterdam University Medical Centers, University of Amsterdam, Meibergdreef 15, 1105 AZ, Amsterdam, The Netherlands.
Experimental Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.
J Cardiovasc Transl Res. 2021 Feb;14(1):13-22. doi: 10.1007/s12265-020-09994-3. Epub 2020 Mar 28.
Chronic inflammation drives the development of atherosclerosis. Despite optimal treatment of classical cardiovascular risk factors, a substantial portion of the population has elevated inflammatory biomarkers and develops atherosclerosis-related complications, indicating that a residual inflammatory risk drives atherosclerotic cardiovascular disease in these patients. Additional anti-inflammatory therapeutic strategies are therefore required. The co-stimulatory molecule CD40 and its ligand CD40L (CD154) have a central role in the regulation of the inflammatory response during the development of atherosclerosis by modulating the interaction between immune cells and between immune cells and non-immune cells. In this review, we discuss the role of the CD40-CD40L dyad in atherosclerosis, and we discuss recent studies on the therapeutic potential of novel CD40-CD40L targeting strategies in cardiovascular medicine.
慢性炎症驱动动脉粥样硬化的发展。尽管对经典心血管危险因素进行了最佳治疗,但仍有相当一部分人群的炎症生物标志物升高,并发生与动脉粥样硬化相关的并发症,这表明在这些患者中,残留的炎症风险会导致动脉粥样硬化性心血管疾病。因此,需要额外的抗炎治疗策略。共刺激分子 CD40 及其配体 CD40L(CD154)在动脉粥样硬化发展过程中通过调节免疫细胞与非免疫细胞之间的相互作用,在炎症反应的调节中发挥核心作用。在这篇综述中,我们讨论了 CD40-CD40L 二聚体在动脉粥样硬化中的作用,并讨论了最近关于新型 CD40-CD40L 靶向策略在心血管医学中治疗潜力的研究。