Tumour priming by ultrasound mechanogenetics for CAR T therapy

Cell-based cancer immunotherapy holds potential as a therapeutic approach, yet its application for solid tumour treatment remains challenging. Here we report a focused-ultrasound-based approach that mechanically induces the localized expression of CD19 antigen within a subpopulation of cells within solid tumours, which function as local 'training centres' to activate chimeric antigen receptor T cells. Activated chimeric antigen receptor T cells attack the whole cancer cell population near the tumour site, thus achieving cancer suppression. The system achieves targeted gene expression by integrating focused-ultrasound-triggered mechanical stimulation and the subsequent calcium response of cancer cells with a doxycycline-gated AND-logic genetic circuit, both of which need to be active for effective induction of CD19 expression. We validate the functionality of the approach in vitro, in organoids and in vivo, achieving direct control of user-designed gene expressions through FUS-mediated mechanical stimulation without the need of any cofactor, demonstrating the approach's potential as a versatile platform for precisely controllable immunotherapy. Overall, our combinatorial approach offers a focused-ultrasound-controlled remote and non-invasive priming of solid tumours for effective and safe chimeric antigen receptor T cell immunotherapy via the induced production of clinically validated antigens.

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Publication Details

Journal
Nature Materials
Published
2025-10-31
DOI
https://doi.org/10.1038/s41563-025-02391-8
Citations
1
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
1.05

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article

Tumour priming by ultrasound mechanogenetics for CAR T therapy

Yushun Zeng, Gengxi Lu, Longwei Liu, Christina Jamieson et al.
1 citations
Nature Materials
CAR-T cell therapy research
1.05
article

Tumour priming by ultrasound mechanogenetics for CAR T therapy

Yushun Zeng, Gengxi Lu, Longwei Liu, Christina Jamieson, Bingfei Yu, Priyankan Datta, Yunjia Qu, Yingxiao Wang, Linshan Zhu, Qifa Zhou, Ziliang Huang, Ruimin Chen, Yuxuan Wang, Phuong Ho, Xi Yu, Fan Wei, Ali Zamat, Alexa Lewis, Chunyang Song, K. Kirk Shung, Chi Woo Yoon, Dung Ngo Minh Nguyen, Nan Sook Lee
article en
1 citations

Abstract

Cell-based cancer immunotherapy holds potential as a therapeutic approach, yet its application for solid tumour treatment remains challenging. Here we report a focused-ultrasound-based approach that mechanically induces the localized expression of CD19 antigen within a subpopulation of cells within solid tumours, which function as local 'training centres' to activate chimeric antigen receptor T cells. Activated chimeric antigen receptor T cells attack the whole cancer cell population near the tumour site, thus achieving cancer suppression. The system achieves targeted gene expression by integrating focused-ultrasound-triggered mechanical stimulation and the subsequent calcium response of cancer cells with a doxycycline-gated AND-logic genetic circuit, both of which need to be active for effective induction of CD19 expression. We validate the functionality of the approach in vitro, in organoids and in vivo, achieving direct control of user-designed gene expressions through FUS-mediated mechanical stimulation without the need of any cofactor, demonstrating the approach's potential as a versatile platform for precisely controllable immunotherapy. Overall, our combinatorial approach offers a focused-ultrasound-controlled remote and non-invasive priming of solid tumours for effective and safe chimeric antigen receptor T cell immunotherapy via the induced production of clinically validated antigens.

Nature MaterialsVol. 25(2)
University of Southern California (US), University of California San Diego (US), Southern California Eye Institute (US), La Jolla Bioengineering Institute (US)
Parker Institute for Cancer Immunotherapy, National Institutes of Health, University of California, San Diego, National Cancer Institute
Openalex Percentile: Top 16%
CAR-T cell therapy research
1.05
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