Marengo Marita, Migliori Massimiliano, Merlotti Guido, Fabbrini Paolo, Panichi Vincenzo, Cantaluppi Vincenzo
Nephrology and Dialysis Unit, ASL CN1, Cuneo, Italy.
Nephrology and Dialysis Unit, "Versilia" Hospital, Camaiore, Italy.
Blood Purif. 2023;52 Suppl 1(Suppl 1):27-42. doi: 10.1159/000530808. Epub 2023 Jun 16.
Despite the recent advances in dialysis technology, mortality rate of chronic uremic patients still remains excessively high: of note, in comparison to age- and sex-matched healthy controls, this frail population shows a higher incidence of infections, cancer, cognitive decline, and, in particular, major adverse cardiovascular events (MACE) that represent nowadays the first cause of mortality. Several traditional and nontraditional factors contribute to this increased risk for MACE and accelerated cellular senescence: among these, inflammation has been shown to play a key role. The costimulatory pathway CD40-CD40 Ligand (CD40L) is harmfully activated during inflammation and uremia-associated clinical complications: in particular, the soluble form of CD40L (sCD40L) can bind to the CD40 receptor triggering a cascade of detrimental pathways in immune and nonimmune cells. In this narrative review, we summarize the current concepts of the biological role of the CD40-CD40L pathway in uremia-associated organ dysfunction, focusing on the above-described main causes of mortality. Moreover, we discuss the interaction of the CD40-CD40L pathway with extracellular vesicles, microparticles recently identified as new uremic toxins. The biological effects of sCD40L in MACE, cognitive decline, infections, and cancer will be also briefly commented. Last, based on recent studies and ongoing clinical trials, we herein describe the modulatory activity of adsorptive dialysis membranes in polymethylmethacrylate on CD40-CD40L detrimental activation.
尽管透析技术最近取得了进展,但慢性尿毒症患者的死亡率仍然过高:值得注意的是,与年龄和性别匹配的健康对照组相比,这一脆弱人群感染、癌症、认知衰退的发生率更高,尤其是主要不良心血管事件(MACE),目前已成为首要死因。多种传统和非传统因素导致了MACE风险增加和细胞衰老加速:其中,炎症已被证明起关键作用。共刺激通路CD40 - CD40配体(CD40L)在炎症和尿毒症相关临床并发症期间被有害激活:特别是,可溶性CD40L(sCD40L)可与CD40受体结合,在免疫和非免疫细胞中触发一系列有害途径。在这篇叙述性综述中,我们总结了CD40 - CD40L通路在尿毒症相关器官功能障碍中的生物学作用的当前概念,重点关注上述主要死因。此外,我们讨论了CD40 - CD40L通路与细胞外囊泡、最近被确定为新的尿毒症毒素的微粒之间的相互作用。还将简要评论sCD40L在MACE、认知衰退、感染和癌症中的生物学效应。最后,基于最近的研究和正在进行的临床试验,我们在此描述聚甲基丙烯酸甲酯吸附性透析膜对CD40 - CD40L有害激活的调节活性。