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Updated: Sep 3, 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
3D ex vivo platform for high-throughput immunotherapy screening in relapsed/refractory lymphoma patients
Fabien Gava1,2,3,4,5, Paul Marcoux1,2,3,4, Neus Serrat6,7
1Univ Toulouse, INSERM, CRCT Toulouse France.
Abstract:
Relapsed/refractory (R/R) B-cell lymphomas (B-NHL) remain incurable, with limited predictive biomarkers to guide immunotherapy. Preclinical platforms that faithfully preserve the immune context and the viability of patient samples are critically needed for relevant high-throughput drug testing. Here, we present a 3D ex vivo platform for immunotherapy screening that generates patient-derived lymphoma spheroids (PDLS) a scaffold- and matrix-free 3D model derived from peripheral blood or lymph node biopsies of patients, including R/R follicular lymphoma, transformed follicular lymphoma, or diffuse large B-cell lymphoma. PDLS maintain the cellular composition, T-cell activation, and immune escape profiles of the original tumors, supporting multiplexed screening of single-agent and combination therapies within clinically relevant time frames. This scalable model recapitulates immune-tumor cell interactions, provides rapid assessment of immunotherapy efficacy, and bridges preclinical research with clinical application in aggressive B-cell lymphomas. By integrating spatial profiling and single-cell RNA sequencing, PDLS can further evolve into patient-specific 3D tumor avatars that support precision oncology approaches in aggressive B-NHL.
