Publication: An 89Zr-HDL PET Tracer Monitors Response to a CSF1R Inhibitor
| dc.contributor.author | Mason, Christian A | |
| dc.contributor.author | Kossatz, Susanne | |
| dc.contributor.author | Carter, Lukas M | |
| dc.contributor.author | Pirovano, Giacomo | |
| dc.contributor.author | Brand, Christian | |
| dc.contributor.author | Guru, Navjot | |
| dc.contributor.author | Perez-Medina, Carlos | |
| dc.contributor.author | Lewis, Jason S | |
| dc.contributor.author | Mulder, Willem J M | |
| dc.contributor.author | Reiner, Thomas | |
| dc.contributor.funder | National Institutes of Health (Estados Unidos) | |
| dc.date.accessioned | 2020-03-25T10:51:36Z | |
| dc.date.available | 2020-03-25T10:51:36Z | |
| dc.date.issued | 2020-03 | |
| dc.description.abstract | The 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.peerreviewed | Sí | es_ES |
| dc.description.sponsorship | We 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.number | 3 | es_ES |
| dc.format.page | 433-436 | es_ES |
| dc.format.volume | 61 | es_ES |
| dc.identifier.citation | J Nucl Med. 2020; 61(3):433-436 | es_ES |
| dc.identifier.doi | 10.2967/jnumed.119.230466 | es_ES |
| dc.identifier.e-issn | 1535-5667 | es_ES |
| dc.identifier.issn | 0161-5505 | es_ES |
| dc.identifier.journal | Journal of nuclear medicine : official publication, Society of Nuclear Medicine | es_ES |
| dc.identifier.pubmedID | 31420495 | es_ES |
| dc.identifier.uri | http://hdl.handle.net/20.500.12105/9326 | |
| dc.language.iso | eng | es_ES |
| dc.publisher | Society of Nuclear Medicine and Molecular Imaging (SNMMI) | es_ES |
| dc.relation.publisherversion | https://doi.org/10.2967/jnumed.119.230466 | es_ES |
| dc.repisalud.institucion | CNIC | es_ES |
| dc.repisalud.orgCNIC | CNIC::Grupos de investigación | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Atribución 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.subject | CSF1R inhibitor | es_ES |
| dc.subject | HDL | es_ES |
| dc.subject | PET/CT imaging | es_ES |
| dc.subject | Immunotherapy | es_ES |
| dc.subject | Tumor-associated macrophages | es_ES |
| dc.title | An 89Zr-HDL PET Tracer Monitors Response to a CSF1R Inhibitor | es_ES |
| dc.type | journal article | es_ES |
| dc.type.hasVersion | VoR | es_ES |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 83f5958f-fd59-4a29-90b6-e4d6e25a24e4 | |
| relation.isAuthorOfPublication.latestForDiscovery | 83f5958f-fd59-4a29-90b6-e4d6e25a24e4 |
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