Lavine Kory J, Sultan Deborah, Luehmann Hannah, Detering Lisa, Zhang Xiaohui, Heo Gyu Seong, Zhang Xiuli, Hoelscher Michelle, Harrison Kitty, Combadière Christophe, Laforest Richard, Kreisel Daniel, Woodard Pamela K, Brody Steven L, Gropler Robert J, Liu Yongjian
Department of Medicine, Washington University School of Medicine, St. Louis, MO USA.
Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO USA.
Nat Cardiovasc Res. 2023 Oct;2(10):874-880. Epub 2023 Sep 21.
Among the diverse populations of myeloid cells that reside within the healthy and diseased heart, C-C chemokine receptor 2 (CCR2) is specifically expressed on inflammatory populations of monocytes and macrophages that contribute to the development and progression of heart failure. Here, we evaluated a peptide-based imaging probe (Cu-DOTA-ECL1i) that specifically recognizes CCR2 monocytes and macrophages for human cardiac imaging. Compared to healthy controls, Cu-DOTA-ECL1i heart uptake was increased in subjects following acute myocardial infarction, predominately localized within the infarct area, and was associated with impaired myocardial wall motion. These findings establish the feasibility of molecular imaging of CCR2 expression to visualize inflammatory monocytes and macrophages in the injured human heart.
在健康和患病心脏中存在的多种髓样细胞群体中,C-C趋化因子受体2(CCR2)在炎症性单核细胞和巨噬细胞群体上特异性表达,这些细胞有助于心力衰竭的发生和发展。在此,我们评估了一种基于肽的成像探针(Cu-DOTA-ECL1i),其可特异性识别CCR2单核细胞和巨噬细胞用于人体心脏成像。与健康对照相比,急性心肌梗死后受试者的Cu-DOTA-ECL1i心脏摄取增加,主要定位于梗死区域,并与心肌壁运动受损相关。这些发现确立了对CCR2表达进行分子成像以可视化受损人心脏中炎症性单核细胞和巨噬细胞的可行性。