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Non-Invasive Imaging of Vascular Inflammation

机译:血管炎症的非侵入性成像

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摘要

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 [18F]-fluorodeoxyglucose and the new [11C]-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.
机译:在大血管血管炎中,炎性浸润可引起受累动脉血管壁增厚,导致进行性狭窄和闭塞。可能还会出现扩张,动脉瘤形成和血栓形成。活化的巨噬细胞和T淋巴细胞是血管炎症的基本要素。炎性浸润的数量和密度与局部疾病活动直接相关。此外,与年龄相匹配的健康个体相比,自身免疫性疾病的患者由于动脉粥样硬化加速而具有更高的心血管(CV)风险。针对活化的巨噬细胞,新血管形成或增加的细胞代谢活性的分子成像技术可以代表无创检测血管炎症的有效手段。在当前的审查中,将介绍已在人类中成功测试的新型非侵入性成像工具。这些包括超声造影,可以检测到发炎动脉壁内的新血管;对比增强的CV磁共振,可以分别使用T2和对比后的T1加权序列检测通常与水肿或壁厚增加有关的动脉壁厚度;以及与[ 18 F]-氟脱氧葡萄糖等放射性示踪剂相关的正电子发射断层扫描和新型[ 11 C] -PK11195结合计算机断层摄影血管造影以检测活化的巨噬细胞在血管壁内。成像技术可用于大血管和中脉血管炎的诊断检查,以监测疾病活动和对治疗的反应。最后,分子成像靶标可以为涉及动脉血管的免疫介导的疾病的发病机理和进化提供新线索。

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