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.

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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
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article

A targeting lentiviral vector for generation of CAR-T cells in vivo

Maoxuan Liu, Zheng Fu, Muhadasi Tuerxunyiming, Ping Zhu et al.
Scientific Reports
CAR-T cell therapy research
article

A targeting lentiviral vector for generation of CAR-T cells in vivo

Maoxuan Liu, Zheng Fu, Muhadasi Tuerxunyiming, Ping Zhu, Jianguo Michael Yin, Qing Zhao
article en

Abstract

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.

Scientific ReportsVol. 16(1)
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)
Good health and well-being
Openalex Percentile: Top 20%
CAR-T cell therapy research
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