Miniature and versatile genome regulation TnpB-ωRNA toolkits facilitate cancer immunotherapy
CRISPR‒Cas systems represent powerful tools for genome regulation. However, the large size of Cas proteins limits their efficient delivery via an adeno-associated virus (AAV), thereby restricting their clinical translation. Here, we engineer the IS200/IS605 transposon-encoded nuclease TnpB, along with its ωRNA scaffold, to create an enhanced TnpB system, which serves as a compact toolkit for gene activation, genome editing, and base editing. The gene activator enTnpBa increases expression by 2889-fold with a minimized 93 nt ωRNA and robustly activates endogenous genes in mammalian cells. We develop a single-AAV-based regimen for immune activation (AAV-ImmunAct) that delivers enTnpBa to activate CXCL9, IL-15, and IFN-γ. AAV-ImmunAct effectively enhances T cell migration and activation, increases killing of cancer cell lines and patient-derived organoids, and synergizes with anti-PD-1 therapy in humanized mice. Here, we establish enTnpB as a compact and versatile platform for genome regulation and a promising tool for cancer immunotherapy.
Authors
- Tianxin Lin (ORCID: https://orcid.org/0000-0003-3180-8697)
- Jianmei Zhong
- Chaoying Liu (ORCID: https://orcid.org/0000-0003-0484-9522)
- Meifeng Cen (ORCID: https://orcid.org/0009-0009-1908-9299)
- Jiahui Wu (ORCID: https://orcid.org/0009-0007-6778-6764)
- Hengji Zhan (ORCID: https://orcid.org/0000-0001-8574-9106)
- Zehua Chen (ORCID: https://orcid.org/0000-0003-2127-7829)
- Jianhui Zhang (ORCID: https://orcid.org/0000-0002-6362-4027)
- Baoqing He
- Kaiwen Jie
- Bolin Pan
- Junlin Lu
- Qiang Zhang
- Xu Chen
- Jiajian Lai
Institutions
- Sun Yat-sen University (CN)
- Sun Yat-sen Memorial Hospital (CN)
- Fifth Affiliated Hospital of Sun Yat-sen University (CN)
- University of Virginia (US)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-04-01
- DOI
- https://doi.org/10.1038/s41467-026-71327-w
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 0.00