Publication:
An 89Zr-HDL PET Tracer Monitors Response to a CSF1R Inhibitor

dc.contributor.authorMason, Christian A
dc.contributor.authorKossatz, Susanne
dc.contributor.authorCarter, Lukas M
dc.contributor.authorPirovano, Giacomo
dc.contributor.authorBrand, Christian
dc.contributor.authorGuru, Navjot
dc.contributor.authorPerez-Medina, Carlos
dc.contributor.authorLewis, Jason S
dc.contributor.authorMulder, Willem J M
dc.contributor.authorReiner, Thomas
dc.contributor.funderNational Institutes of Health (Estados Unidos)
dc.date.accessioned2020-03-25T10:51:36Z
dc.date.available2020-03-25T10:51:36Z
dc.date.issued2020-03
dc.description.abstractThe immune function within the tumor microenvironment has become a prominent therapeutic target, with tumor-associated macrophages (TAMs) playing a critical role in immune suppression. We propose an 89Zr-labeled high-density lipoprotein (89Zr-HDL) nanotracer as a means of monitoring response to immunotherapy. Methods: Female MMTV-PyMT mice were treated with pexidartinib, a colony-stimulating factor 1 receptor (CSF1R) inhibitor, to reduce TAM density. The accumulation of 89Zr-HDL within the tumor was assessed using PET/CT imaging and autoradiography, whereas TAM burden was determined using immunofluorescence. Results: A significant reduction in 89Zr-HDL accumulation was observed in PET/CT images, with 2.9% ± 0.3% and 3.7% ± 0.2% injected dose/g for the pexidartinib- and vehicle-treated mice, respectively. This reduction was corroborated ex vivo and correlated with decreased TAM density. Conclusion: These results support the potential use of 89Zr-HDL nanoparticles as a PET tracer to quickly monitor the response to CSF1R inhibitors and other therapeutic strategies targeting TAMs.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipWe thank the Small Animal Imaging Core, the Radiochemistry and Molecular Imaging Probes Core, and the Molecular Cytology Core at Memorial Sloan Kettering Cancer Center. This work was supported by National Institutes of Health grants R01 CA204441, P30 CA008748 and R01 CA220234. The authors thank the Tow Foundation and Memorial Sloan Kettering Cancer Center's Center for Molecular Imaging & Nanotechnology (CMINT), the Imaging and Radiation Sciences Program and the MSK Molecularly Targeted Intraoperative Imaging Fund.es_ES
dc.format.number3es_ES
dc.format.page433-436es_ES
dc.format.volume61es_ES
dc.identifier.citationJ Nucl Med. 2020; 61(3):433-436es_ES
dc.identifier.doi10.2967/jnumed.119.230466es_ES
dc.identifier.e-issn1535-5667es_ES
dc.identifier.issn0161-5505es_ES
dc.identifier.journalJournal of nuclear medicine : official publication, Society of Nuclear Medicinees_ES
dc.identifier.pubmedID31420495es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/9326
dc.language.isoenges_ES
dc.publisherSociety of Nuclear Medicine and Molecular Imaging (SNMMI)es_ES
dc.relation.publisherversionhttps://doi.org/10.2967/jnumed.119.230466es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigaciónes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectCSF1R inhibitores_ES
dc.subjectHDLes_ES
dc.subjectPET/CT imaginges_ES
dc.subjectImmunotherapyes_ES
dc.subjectTumor-associated macrophageses_ES
dc.titleAn 89Zr-HDL PET Tracer Monitors Response to a CSF1R Inhibitores_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication83f5958f-fd59-4a29-90b6-e4d6e25a24e4
relation.isAuthorOfPublication.latestForDiscovery83f5958f-fd59-4a29-90b6-e4d6e25a24e4

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