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Immuno-PET Imaging of Atherosclerotic Plaques with [89Zr]Zr-Anti-CD40 mAb-Proof of Concept.
Poels, Kikkie; Schreurs, Maxime; Jansen, Matthijs; Vugts, Danielle J; Seijkens, Tom T P; van Dongen, Guus A M S; Lutgens, Esther; Beaino, Wissam.
Afiliação
  • Poels K; Department of Medical Biochemistry, Amsterdam Cardiovascular Sciences (ACS), Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
  • Schreurs M; Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Unversiteit, 1081 HV Amsterdam, The Netherlands.
  • Jansen M; Department of Medical Biochemistry, Amsterdam Cardiovascular Sciences (ACS), Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
  • Vugts DJ; Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Unversiteit, 1081 HV Amsterdam, The Netherlands.
  • Seijkens TTP; Department of Medical Biochemistry, Amsterdam Cardiovascular Sciences (ACS), Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
  • van Dongen GAMS; Department of Medical Oncology, Antoni van Leeuwenhoek-Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
  • Lutgens E; Department of Radiology and Nuclear Medicine, Amsterdam UMC, Vrije Unversiteit, 1081 HV Amsterdam, The Netherlands.
  • Beaino W; Department of Medical Biochemistry, Amsterdam Cardiovascular Sciences (ACS), Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
Biology (Basel) ; 11(3)2022 Mar 06.
Article em En | MEDLINE | ID: mdl-35336782
ABSTRACT
Non-invasive imaging of atherosclerosis can help in the identification of vulnerable plaque lesions. CD40 is a co-stimulatory molecule present on various immune and non-immune cells in the plaques and is linked to inflammation and plaque instability. We hypothesize that a 89Zr-labeled anti-CD40 monoclonal antibody (mAb) tracer has the potential to bind to cells present in atherosclerotic lesions and that CD40 Positron Emission Tomography (PET) can contribute to the detection of vulnerable atherosclerotic plaque lesions. To study this, wild-type (WT) and ApoE-/- mice were fed a high cholesterol diet for 14 weeks to develop atherosclerosis. Mice were injected with [89Zr]Zr-anti-CD40 mAb and the aortic uptake was evaluated and quantified using PET/Computed Tomography (CT) imaging. Ex vivo biodistribution was performed post-PET imaging and the uptake in the aorta was assessed with autoradiography and compared with Oil red O staining to determine the tracer potential to detect atherosclerotic plaques. On day 3 and 7 post injection, analysis of [89Zr]Zr-anti-CD40 mAb PET/CT scans showed a more pronounced aortic signal in ApoE-/- compared to WT mice with an increased aorta-to-blood uptake ratio. Autoradiography revealed [89Zr]Zr-anti-CD40 mAb uptake in atherosclerotic plaque areas in ApoE-/- mice, while no signal was found in WT mice. Clear overlap was observed between plaque areas as identified by Oil red O staining and autoradiography signal of [89Zr]Zr-anti-CD40 mAb in ApoE-/- mice. In this proof of concept study, we showed that PET/CT with [89Zr]Zr-anti-CD40 mAb can detect atherosclerotic plaques. As CD40 is associated with plaque vulnerability, [89Zr]Zr-anti-CD40 mAb has the potential to become a tracer to detect vulnerable atherosclerotic plaques.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article