<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-30T03:03:41Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/9326" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/9326</identifier><datestamp>2024-09-27T09:09:36Z</datestamp><setSpec>com_20.500.12105_19604</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19605</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Mason, Christian A</subfield>
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      <subfield code="a">Kossatz, Susanne</subfield>
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      <subfield code="a">Carter, Lukas M</subfield>
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      <subfield code="a">Pirovano, Giacomo</subfield>
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      <subfield code="a">Brand, Christian</subfield>
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      <subfield code="a">Guru, Navjot</subfield>
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      <subfield code="a">Perez-Medina, Carlos</subfield>
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      <subfield code="a">Lewis, Jason S</subfield>
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      <subfield code="a">Mulder, Willem J M</subfield>
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      <subfield code="a">Reiner, Thomas</subfield>
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      <subfield code="a">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.</subfield>
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      <subfield code="a">J Nucl Med. 2020; 61(3):433-436</subfield>
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      <subfield code="a">10.2967/jnumed.119.230466</subfield>
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      <subfield code="a">Journal of nuclear medicine : official publication, Society of Nuclear Medicine</subfield>
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      <subfield code="a">31420495</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/9326</subfield>
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      <subfield code="a">CSF1R inhibitor</subfield>
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      <subfield code="a">HDL</subfield>
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      <subfield code="a">Tumor-associated macrophages</subfield>
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      <subfield code="a">An 89Zr-HDL PET Tracer Monitors Response to a CSF1R Inhibitor</subfield>
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