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.
Original language | English |
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Pages (from-to) | 433-436 |
Number of pages | 4 |
Journal | Journal of Nuclear Medicine |
Volume | 61 |
Issue number | 3 |
DOIs | |
State | Published - 1 Mar 2020 |
Keywords
- CSF1R inhibitor
- HDL
- Immunotherapy
- PET/CT imaging
- Tumor-Associated macrophages