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Date publication

mai 2015

Journal

Nanomedicine : nanotechnology, biology, and medicine

Auteurs

Membres identifiés du Cancéropôle Est :
Dr BOUDON Julien


Tous les auteurs :
Jacobin-Valat MJ, Laroche-Traineau J, Larivière M, Mornet S, Sanchez S, Biran M, Lebaron C, Boudon J, Lacomme S, Cérutti M, Clofent-Sanchez G

Résumé

Atherosclerosis is an inflammatory disease associated with the formation of atheroma plaques likely to rupture in which platelets are involved both in atherogenesis and atherothrombosis. The rupture is linked to the molecular composition of vulnerable plaques, causing acute cardiovascular events. In this study we propose an original targeted contrast agent for molecular imaging of atherosclerosis. Versatile USPIO (VUSPIO) nanoparticles, enhancing contrast in MR imaging, were functionalised with a recombinant human IgG4 antibody, rIgG4 TEG4, targeting human activated platelets. The maintenance of immunoreactivity of the targeted VUSPIO against platelets was confirmed in vitro by flow cytometry, transmission electronic and optical microscopy. In the atherosclerotic ApoE(-/-) mouse model, high-resolution ex vivo MRI demonstrated the selective binding of TEG4-VUSPIO on atheroma plaques. It is noteworthy that the rationale for targeting platelets within atherosclerotic lesions is highlighted by our targeted contrast agent using a human anti-αIIbβ3 antibody as a targeting moiety.

Mots clés

Animals, Antibodies, Monoclonal, chemistry, Blood Platelets, Contrast Media, chemistry, Disease Models, Animal, Humans, Mice, Mice, Knockout, Molecular Imaging, methods, Nanoparticles, chemistry, Plaque, Atherosclerotic, metabolism, Platelet Glycoprotein GPIIb-IIIa Complex

Référence

Nanomedicine. 2015 May;11(4):927-37