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Published on: February 17, 2022
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Visualizing CAR-T cell Immunotherapy Using 3 Tesla Fluorine-19 MRI.
Veronica P Dubois1,2, Olivia C Sehl1,2, Paula J Foster1,2
1Robarts Research Institute, London, ON, Canada.
Molecular Imaging and Biology
|November 17, 2021
Summary
Fluorine-19 (19F) magnetic resonance imaging (MRI) successfully visualized perfluorocarbon (PFC)-labeled chimeric antigen receptor (CAR) T cells in a leukemia mouse model. PFC labeling did not impact CAR T-cell effectiveness, showing promise for tracking cell therapies.
Area of Science:
- Oncology
- Immunotherapy
- Biomedical Imaging
Background:
- Chimeric antigen receptor (CAR) T cell therapy shows promise for hematological malignancies but faces challenges with patient response, side effects, and solid tumor treatment.
- An effective imaging tool is needed to track CAR T-cell location, predict treatment success, and identify off-target toxicities.
Purpose of the Study:
- To visualize perfluorocarbon (PFC)-labeled CAR T-cells in a mouse leukemia model using 3 Tesla 19F MRI.
- To compare the in vivo cytotoxicity of PFC-labeled CAR T-cells versus unlabeled CAR T-cells.
Main Methods:
- NSG mice with established leukemia received intratumoral injections of PFC-labeled CAR T-cells, unlabeled CAR T-cells, PFC-labeled untransduced T-cells, or saline.
- 19F MRI was used to detect PFC-labeled CAR T-cells at multiple time points post-injection.
- Bioluminescence imaging (BLI) monitored tumor progression in all groups.
Main Results:
- 19F MRI successfully detected PFC-labeled CAR T-cells in tumors up to 7 days post-injection.
- Both PFC-labeled and unlabeled CAR T-cells significantly reduced tumor burden compared to controls (p < 0.05).
- No significant difference in cytotoxicity was observed between PFC-labeled and unlabeled CAR T-cells.
Conclusions:
- Clinical field strength 19F MRI can effectively visualize PFC-labeled CAR T-cells in vivo for up to 7 days.
- PFC labeling does not compromise the in vivo efficacy of CAR T-cells.
- This imaging approach holds potential for tracking CAR T-cell therapies in preclinical studies and future clinical applications, particularly for localized CAR T-cell injections.

