A targeting lentiviral vector for generation of CAR-T cells in vivo
Chimeric antigen receptor (CAR) T cell therapy has demonstrated remarkable therapeutic efficacy in treating cancer and autoimmune diseases. However, current CAR-T cell therapy requires ex vivo T cell engineering, which is both time-consuming and cost-prohibitive, adding complexity to the overall treatment. In this study, using an engineered Sindbis virus envelope, we developed a lentiviral vector system with high specificity for targeting human T cell line and primary T cells, but not targeting other immune cell subsets. Notably, this T cell-specific lentiviral vector does not require additional anti-CD3/CD28 stimulation for primary T cell activation during infection in vitro. Furthermore, the lentiviral vector successfully delivered a CD19-targeting CAR molecule to human primary T cells in vivo. The in vivo generated CD19-CAR-T cells efficiently mediated B cell lymphoma clearance. Overall, our study provides a promising tool for the development of in vivo T cell engineering approaches.
Authors
- Maoxuan Liu (ORCID: https://orcid.org/0000-0002-0953-9673)
- Zheng Fu
- Muhadasi Tuerxunyiming
- Ping Zhu
- Jianguo Michael Yin
- Qing Zhao
Institutions
- Xuzhou Medical College (CN)
- Second People’s Hospital of Huai’an (CN)
- Shenzhen Institutes of Advanced Technology (CN)
- Viva Biotech (China) (CN)
- Hangzhou City University
- Xi’an Jiaotong-Liverpool University (CN)
- Zhejiang University (CN)
- Nanjing Medical University (CN)
Publication Details
- Journal
- Scientific Reports
- Published
- 2026-03-17
- DOI
- https://doi.org/10.1038/s41598-025-17342-1
- Primary Topic
- CAR-T cell therapy research
- Type
- article
- Field-Weighted Citation Impact
- 0.00