In situ T cell transfection methods overcome the complexity and high costs associated with conventional chimeric antigen receptor (CAR)-T therapy. However, the in situ CAR-T cell approach operates within the patient's complex immune environment and bypasses preinfusion ex vivo cellular quality controls, necessitating advanced imaging techniques to track immune cell migration and function. Positron emission tomography (PET) can detect biochemical processes in patients and, when combined with a radiotracer specific for the engineered cells, can monitor CAR-T cell trafficking. Herein, we develop an approach for in situ T cell generation, tracking, and functional assessment using anti-CD5-conjugated lipid nanoparticles for codelivering CD19 CAR mRNA (mCAR19) and a prostate-specific membrane antigen mRNA (mPSMA) tag. With interleukin-7 (IL-7) preconditioning and repeated administration, this approach achieves tumor-free survival in 75% of B cell lymphoma-bearing mice (similar efficacy to ex vivo approaches), and through PET imaging of (68)Ga-PSMA-617, the generation and tumor infiltration of in situ-engineered PSMA-tagged CD19 CAR-T cells is validated.
Development of an in situ CAR-T cell protocol through optical and PSMA-targeted PET imaging.
通过光学和PSMA靶向PET成像开发原位CAR-T细胞方案
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作者:Zhang Nisi, Seo Jai Woong, Robinson Elise, Rivera-Rodriguez Angelie, Wang James, Guo Yutong, Czerwinski Debra K, Kim Ha Rin, Tumbale Spencer K, Raie Marina N, Jan Basit L, Engudar Gokce, Sallets Adrienne, Minn Il, Pomper Martin G, Levy Ronald, Ferrara Katherine W
| 期刊: | Proceedings of the National Academy of Sciences of the United States of America | 影响因子: | 9.100 |
| 时间: | 2025 | 起止号: | 2025 Jun 17; 122(24):e2504950122 |
| doi: | 10.1073/pnas.2504950122 | 研究方向: | 细胞生物学 |
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