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PET and SPECT Imaging of Macrophages in the Tumor Stroma: An Update
Shaobo Li1,2, Alex Maes3,4, Tijl Vermassen2,5,6
1Department of Diagnostic Sciences, Ghent University, Corneel Heymanslaan 10, 9000 Ghent, Belgium.
Abstract:
Tumor-associated macrophages (TAMs) are pivotal immune cells within the tumor stroma, whose dynamic alterations significantly impact tumor progression and therapeutic responses. Conventional methods for TAM detection, such as biopsy, are invasive and incapable of whole-body dynamic monitoring. In contrast, positron emission tomography (PET) and single-photon emission computed tomography (SPECT) offer a non-invasive imaging approach by targeting TAM-specific biomarkers like CD206, TSPO, and CCR2. This review comprehensively summarizes the advancements in TAM-targeted imaging probes, including cell surface markers, metabolic/functional markers, and multifunctional nanoprobe, while assessing their potential in tumor immune surveillance and tumor targeting therapeutic applications. While current probes, including 68Ga-NOTA-anti-CD206 and 64Cu-Macrin, have exhibited high specificity and theragnostic potential in preclinical and early clinical trials, challenges such as target heterogeneity, off-target effects, and clinical translation persist. Moving forward, the advancement of multi-target probes, optimization of pharmacokinetics, and incorporation of multimodal imaging technologies are anticipated to further enhance the impact of TAM-targeted imaging in precision medicine and tumor immunotherapy, fostering the refinement of personalized treatment strategies and improving patient outcomes.
Insights
Non-invasive imaging using PET and SPECT can track tumor-associated macrophages (TAMs) by targeting biomarkers. Advancements in TAM-targeted probes show promise for tumor immune surveillance and therapy, aiding personalized medicine.
Area of Science:
- Oncology
- Immunology
- Medical Imaging
Background:
- Tumor-associated macrophages (TAMs) are crucial immune cells influencing tumor progression and treatment outcomes.
- Traditional TAM detection methods like biopsy are invasive and lack whole-body dynamic monitoring capabilities.
- Positron emission tomography (PET) and single-photon emission computed tomography (SPECT) offer non-invasive imaging alternatives.
Purpose of the Study:
- To review advancements in TAM-targeted imaging probes for non-invasive tumor immune surveillance.
- To assess the potential of these probes in tumor targeting and therapeutic applications.
- To highlight challenges and future directions in TAM-targeted imaging for precision medicine.
Main Methods:
- Comprehensive review of literature on TAM-targeted imaging probes.
- Analysis of probes targeting cell surface markers (e.g., CD206), metabolic/functional markers (e.g., TSPO, CCR2), and multifunctional nanoprobes.
- Evaluation of theragnostic potential in preclinical and early clinical studies.
Main Results:
- Various TAM-specific biomarkers (CD206, TSPO, CCR2) are targeted by advanced imaging probes.
- Probes like 68Ga-NOTA-anti-CD206 and 64Cu-Macrin demonstrate high specificity and theragnostic potential.
- Challenges include target heterogeneity, off-target effects, and clinical translation hurdles.
Conclusions:
- TAM-targeted imaging offers a non-invasive approach for monitoring tumor immunity and guiding therapy.
- Further development of multi-target probes and multimodal imaging is essential for clinical translation.
- Optimized TAM imaging will enhance precision medicine and personalize cancer treatment strategies.
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