Department of Molecular Cardiology, Heinrich Heine University Düsseldorf, Universitätsstraße 1, 40225, Düsseldorf, Germany.
MAGMA. 2014 Feb;27(1):101-6. doi: 10.1007/s10334-013-0391-6. Epub 2013 Jul 4.
OBJECTIVE: This paper introduces a new approach permitting for the first time a specific, non-invasive diagnosis of myocarditis by visualizing the infiltration of immune cells into the myocardium. MATERIALS AND METHODS: The feasibility of this approach is shown in a murine model of viral myocarditis. Our study uses biochemically inert perfluorocarbons (PFCs) known to be taken up by circulating monocytes/macrophages after intravenous injection. RESULTS: In vivo (19)F MRI at 9.4 T demonstrated that PFC-loaded immune cells infiltrate into inflamed myocardial areas. Because of the lack of any fluorine background in the body, detected (19)F signals of PFCs are highly specific as confirmed ex vivo by flow cytometry and histology. CONCLUSION: Since PFCs are a family of compounds previously used clinically as blood substitutes, the technique described in our paper holds the potential as a new imaging modality for the diagnosis of myocarditis in man.
目的:本文提出了一种新方法,首次通过可视化免疫细胞浸润心肌来实现对心肌炎的特异性、非侵入性诊断。
材料和方法:该方法的可行性在病毒性心肌炎的小鼠模型中得到了验证。我们的研究使用了已知在静脉注射后被循环单核细胞/巨噬细胞摄取的生化惰性全氟碳化合物(PFC)。
结果:在 9.4T 的体内(19)F MRI 中显示,负载 PFC 的免疫细胞浸润到炎症心肌区域。由于体内没有任何氟背景,因此通过流式细胞术和组织学证实,检测到的 PFC 的(19)F 信号具有高度特异性。
结论:由于 PFC 是一类先前在临床上用作血液替代品的化合物,因此本文所述的技术有可能成为人类心肌炎诊断的一种新的成像方式。
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