Cardiothoracic Department, San Raffaele Scientific Institute and University , Milan , Italy ; Cardiovascular and Thoracic Department, AO Ospedale Niguarda Ca' Granda , Milan , Italy.
Cardiothoracic Department, San Raffaele Scientific Institute and University , Milan , Italy.
Front Immunol. 2014 Aug 18;5:399. doi: 10.3389/fimmu.2014.00399. eCollection 2014.
In large-vessel vasculitides, inflammatory infiltrates may cause thickening of the involved arterial vessel wall leading to progressive stenosis and occlusion. Dilatation, aneurysm formation, and thrombosis may also ensue. Activated macrophages and T lymphocytes are fundamental elements in vascular inflammation. The amount and density of the inflammatory infiltrate is directly linked to local disease activity. Additionally, patients with autoimmune disorders have an increased cardiovascular (CV) risk compared with age-matched healthy individuals as a consequence of accelerated atherosclerosis. Molecular imaging techniques targeting activated macrophages, neovascularization, or increased cellular metabolic activity can represent effective means of non-invasive detection of vascular inflammation. In the present review, novel non-invasive imaging tools that have been successfully tested in humans will be presented. These include contrast-enhanced ultrasonography, which allows detection of neovessels within the wall of inflamed arteries; contrast-enhanced CV magnetic resonance that can detect increased thickness of the arterial wall, usually associated with edema, or mural enhancement using T2 and post-contrast T1-weighted sequences, respectively; and positron emission tomography associated with radio-tracers such as [(18)F]-fluorodeoxyglucose and the new [(11)C]-PK11195 in combination with computed tomography angiography to detect activated macrophages within the vessel wall. Imaging techniques are useful in the diagnostic work-up of large- and medium-vessel vasculitides, to monitor disease activity and the response to treatments. Finally, molecular imaging targets can provide new clues about the pathogenesis and evolution of immune-mediated disorders involving arterial vessels.
在大血管血管炎中,炎症浸润可导致受累动脉血管壁增厚,导致进行性狭窄和闭塞。扩张、动脉瘤形成和血栓形成也可能随之发生。活化的巨噬细胞和 T 淋巴细胞是血管炎症的基本要素。炎症浸润的数量和密度与局部疾病活动直接相关。此外,由于动脉粥样硬化加速,自身免疫性疾病患者的心血管(CV)风险比年龄匹配的健康个体增加。针对活化的巨噬细胞、新生血管形成或细胞代谢活性增加的分子成像技术可以代表非侵入性检测血管炎症的有效手段。在本综述中,将介绍已在人体中成功测试的新型非侵入性成像工具。这些包括:超声造影,可检测到炎症动脉壁内的新生血管;对比增强心血管磁共振(CVMR),可检测到动脉壁厚度增加,通常与水肿相关,或分别使用 T2 和对比后 T1 加权序列检测壁增强;以及正电子发射断层扫描与放射性示踪剂(如 [(18)F]-氟脱氧葡萄糖)结合计算机断层血管造影术,以检测血管壁内的活化巨噬细胞。成像技术在大血管和中血管血管炎的诊断中有用,可用于监测疾病活动和治疗反应。最后,分子成像靶标可以为涉及动脉血管的免疫介导性疾病的发病机制和演变提供新的线索。