4.6 Article

Nanobody-Facilitated Multiparametric PET/MRI Phenotyping of Atherosclerosis

期刊

JACC-CARDIOVASCULAR IMAGING
卷 12, 期 10, 页码 2015-2026

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jcmg.2018.07.027

关键词

atherosclerosis; molecular imaging; nanobody; PET/MRI

资金

  1. National Institutes of Health [R01 EB009638, P01 HL131478, R01 HL125703, R01 HL118440, P30 CA008748]
  2. American Heart Association [16SDG31390007, 17PRE33660729]
  3. Netherlands Organization for Scientific Research Nederlandse Organisatie voor Wetenschappelijk Onderzoek Vidi
  4. De Drie Lichten Foundation in the Netherlands
  5. Center for Molecular Imaging and Nanotechnology

向作者/读者索取更多资源

OBJECTIVES This study sought to develop an integrative positron emission tomography (PET) with magnetic resonance imaging (MRI) procedure for accurate atherosclerotic plague phenotyping, facilitated by clinically approved and nanobody radiotracers. BACKGROUND Noninvasive characterization of atherosclerosis remains a challenge in clinical practice. The limitations of current diagnostic methods demonstrate that, in addition to atherosclerotic plaque morphology and composition, disease activity needs to be evaluated. METHODS We screened 3 nanobody radiotracers targeted to different biomarkers of atherosclerosis progression, namely vascular cell adhesion molecule (VCAM)-1, lectin-like oxidized low-density lipoprotein receptor (LOX)-1, and macrophage mannose receptor (MMR). The nanobodies, initially radiolabeled with copper-64 ( Cu-64), were extensively evaluated in Apoe(-/-) mice and atherosclerotic rabbits using a combination of in vivo PET/MRI readouts and ex vivo radioactivity counting, autoradiography, and histological analyses. RESULTS The 3 nanobody radiotracers accumulated in atherosclerotic plaques and displayed short circulation times due to fast renal clearance. The MMR nanobody was selected for labeling with gallium-68 (Ga-88), a short-lived radioisotope with high clinical relevance, and used in an ensuing atherosclerosis progression PET/MRI study. Macrophage burden was longitudinally studied by Ga-68-MMR-PET, plaque burden by T2-weighted MRI, and neovascutarization by dynamic contrast-enhanced (DCE) MRI. Additionally, inflammation and microcalcifications were evaluated by fluorine-18 (F-18)-labeled fluorodeoxyglucose (F-18-FDG) and 18 F-sodium fluoride (F-18-NaF) PET, respectively. We observed an increase in all the aforementioned measures as disease progressed, and the imaging signatures correlated with histopathologicat features. CONCLUSIONS We have evaluated nanobody-based radiotracers in rabbits and developed an integrative PET/MRI protocol that allows noninvasive assessment of different processes relevant to atherosclerosis progression. This approach allows the multiparametric study of atherosclerosis and can aid in early stage anti-atherosclerosis drug trials. (C) 2019 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.

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