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Updated: Aug 5, 2026
![Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F62334.jpg&w=3840&q=50)
Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
Published on: February 17, 2022
Engineering Soluble Recombinant BCMA for Ide-Cel Labeling
Ly Phuong Vy Nguyen1, Christelle Oblet1, Alice Barbarin2
1INSERM U1262, UMR CNRS 7276, Université de Limoges, Limoges, France.
Abstract:
Chimeric antigen receptor (CAR)-T-based strategies target the B-cell maturation antigen (BCMA) expressed on the surface of malignant plasma cells in patients with multiple myeloma (MM). Idecabtagene vicleucel (ide-cel), an anti-BCMA CAR-T therapy, has shown promising results in the treatment of relapsed or refractory multiple myeloma (R/RMM). Notably, the extent of CAR-T cell expansion correlates with objective response rates and complete responses, indicating that monitoring CAR-T cells is critical for predicting clinical outcomes in these patients. Although several tools are available to monitor CAR-T cells in patient blood samples, they remain costly, prompting us to develop novel fluorescent and soluble BCMA reagents for CAR-T cell labeling. BCMA is a type III transmembrane protein, and we found that a recombinant construct consisting of the BCMA extracellular domain fused to green fluorescent protein (GFP) failed to traffic through the Golgi apparatus and was not secreted. Incorporation of the interferon-α2 signal peptide restored intracellular trafficking and enabled efficient secretion of soluble BCMA-GFP and BCMA-mCherry fusion proteins. These reagents specifically labeled anti-BCMA CAR-T cells. Overall, our results establish a cost-effective method to generate soluble BCMA probes and provide accessible tools for monitoring CAR-T cells in translational settings.
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