Tumor Priming by Ultrasound Mechanogenetics for with SynNotch CAR T Therapy
Chi Woo YooniD, Chunyang Song, Dung Ngo Minh Nguyen, Linshan ZhuiD, Phuong HoiD, Ziliang HuangiD, Gengxi LuiD, Ali Zamat, Alexa LewisiD, Ruimin CheniD, Yushun ZengiD, Nan Sook Lee, Christina A. M. JamiesoniD, Koping Kirk ShungiD, Qifa ZhouiD, Yingxiao WangiD
Abstract
Cell-based cancer immunotherapy holds potential as a therapeutic approach, yet its application for solid tumor treatment remains challenging. We created a system where focused ultrasound (FUS) is able to remotely stimulate gene expressions in a specific tissue area through mechanical induction, gated by a chemical inducer to minimize the background noise. This system, known as CaDox, integrates FUS-triggered mechanical and calcium stimulation with doxycycline-responsive genetic circuits, which allows the localized expression of the clinically validated and specific antigen CD19 within a subpopulation of cancer cells upon FUS stimulation. These CD19-expressing cells can then function as "training centers" that activate synNotch chimeric antigen receptor (CAR) T cells to generate CARs that recognize a less specific but widespread antigen in cancer cells, thereby attacking and suppress the whole cancer cell population nearby at the tumor site. We validated the functionality of this CaDox system in vitro, in organoids, and in vivo, demonstrating its potential for various cell types and as a versatile platform for precisely controllable immunotherapy. Our combinatorial approach thus offers a FUS-controlled remote and non-invasive priming of solid tumors for effective and safe CAR T immunotherapy via the induced production of clinically validated antigens.
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