Nature Communications · 2024 · 29 citations · 64 references
Life SciencesBiotechnologyOncologyEpigenomicsGenome EditingMolecular OncologyCancer BiotechnologyChimeric Antigen Receptor T-cell TherapyCrispr-based EngineeringCrispr-cas SystemsEpigenome EditingTherapeutic Genome EditingAdeno-associated Viral TransgenesisAdeno-associated Viral VectorsClustered Regularly Interspaced Short Palindromic Repeats DeliveryCrispr ActivationCrispr RegulationCrispr-based Epigenome EditingCrispr-cas Genome EditingT-cell Therapy
There remains a critical need for the precise control of CRISPR (clustered regularly interspaced short palindromic repeats)-based technologies. Here, we engineer a set of inducible CRISPR-based tools controllable by focused ultrasound (FUS), which can penetrate deep and induce localized hyperthermia for transgene activation. We demonstrate the capabilities of FUS-inducible CRISPR, CRISPR activation (CRISPRa), and CRISPR epigenetic editor (CRISPRee) in modulating the genome and epigenome. We show that FUS-CRISPR-mediated telomere disruption primes solid tumours for chimeric antigen receptor (CAR)-T cell therapy. We further deliver FUS-CRISPR in vivo using adeno-associated viruses (AAVs), followed by FUS-induced telomere disruption and the expression of a clinically validated antigen in a subpopulation of tumour cells, functioning as “training centers” to activate synthetic Notch (synNotch) CAR-T cells to produce CARs against a universal tumour antigen to exterminate neighboring tumour cells. The FUS-CRISPR(a/ee) toolbox hence allows the noninvasive and spatiotemporal control of genomic/epigenomic reprogramming for cancer treatment. There remains a critical need for precise control of CRISPR-based technologies. Here, the authors develop a focused ultrasound (FUS)-controllable CRISPR toolbox, allowing the noninvasive and spatiotemporal control of genomic/epigenomic reprogramming for cancer treatment combined with CAR-T therapy.
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