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Quantitative Imaging of Tumor-Associated Macrophages and Their Response to Therapy Using 64Cu-Labeled Macrin
Hye-Yeong Kim1,2, Ran Li1, Thomas S C Ng1
1Center for Systems Biology , Massachusetts General Hospital Research Institute , Boston , Massachusetts 02114 , United States.
Abstract:
Tumor-associated macrophages (TAMs) are widely implicated in cancer progression, and TAM levels can influence drug responses, particularly to immunotherapy and nanomedicines. However, it has been difficult to quantify total TAM numbers and their dynamic spatiotemporal distribution in a non-invasive and translationally relevant manner. Here, we address this need by developing a pharmacokinetically optimized, 64Cu-labeled polyglucose nanoparticle (Macrin) for quantitative positron emission tomography (PET) imaging of macrophages in tumors. By combining PET with high-resolution in vivo confocal microscopy and ex vivo imaging of optically cleared tissue, we found that Macrin was taken up by macrophages with >90% selectivity. Uptake correlated with the content of macrophages in both healthy tissue and tumors ( R2 > 0.9) and showed striking heterogeneity in the TAM content of an orthotopic and immunocompetent mouse model of lung carcinoma. In a proof-of-principle application, we imaged Macrin to monitor the macrophage response to neo-adjuvant therapy, using a panel of chemotherapeutic and γ-irradiation regimens. Multiple treatments elicited 180-650% increase in TAMs. Imaging identified especially TAM-rich tumors thought to exhibit enhanced permeability and retention of nanotherapeutics. Indeed, these TAM-rich tumors accumulated >700% higher amounts of a model poly(d,l-lactic- co-glycolic acid)- b-polyethylene glycol (PLGA-PEG) therapeutic nanoparticle compared to TAM-deficient tumors, suggesting that imaging may guide patient selection into nanomedicine trials. In an orthotopic breast cancer model, chemoradiation enhanced TAM and Macrin accumulation in tumors, which corresponded to the improved delivery and efficacy of two model nanotherapies, PEGylated liposomal doxorubicin and a TAM-targeted nanoformulation of the toll-like receptor 7/8 agonist resiquimod (R848). Thus, Macrin imaging offers a selective and translational means to quantify TAMs and inform therapeutic decisions.
Insights
We developed Macrin, a novel nanoparticle for PET imaging, to quantify tumor-associated macrophages (TAMs). This imaging tool accurately tracks macrophage levels and distribution, aiding in nanomedicine treatment decisions.
Area of Science:
- Biomedical Imaging
- Nanotechnology
- Cancer Biology
Background:
- Tumor-associated macrophages (TAMs) significantly impact cancer progression and drug response.
- Quantifying TAMs non-invasively remains a challenge for treatment optimization.
- Current methods lack translational relevance for dynamic TAM assessment.
Purpose of the Study:
- To develop a quantitative positron emission tomography (PET) imaging agent for macrophages in tumors.
- To assess the utility of this agent in monitoring TAMs during therapy.
- To correlate TAM imaging with nanotherapeutic delivery and efficacy.
Main Methods:
- Development of a 64Cu-labeled polyglucose nanoparticle (Macrin) for PET imaging.
- Combination of PET with in vivo confocal microscopy and ex vivo imaging.
- Validation in orthotopic mouse models of lung and breast carcinoma.
Main Results:
- Macrin demonstrated >90% selectivity for macrophage uptake.
- Macrin uptake strongly correlated with macrophage content in healthy tissues and tumors.
- Imaging revealed significant, therapy-induced increases in TAMs (180-650%).
- TAM-rich tumors showed >700% higher accumulation of therapeutic nanoparticles.
- Macrin imaging correlated with improved nanotherapy delivery and efficacy.
Conclusions:
- Macrin provides a selective and translational method for quantifying TAMs via PET imaging.
- Macrin imaging can monitor therapeutic responses and predict nanomedicine accumulation.
- This approach may guide patient selection for nanomedicine clinical trials.
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