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.

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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
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article

Miniature and versatile genome regulation TnpB-ωRNA toolkits facilitate cancer immunotherapy

Tianxin Lin, Jianmei Zhong, Chaoying Liu, Meifeng Cen et al.
Nature Communications
CRISPR and Genetic Engineering
article

Miniature and versatile genome regulation TnpB-ωRNA toolkits facilitate cancer immunotherapy

Tianxin Lin, Jianmei Zhong, Chaoying Liu, Meifeng Cen, Jiahui Wu, Hengji Zhan, Zehua Chen, Jianhui Zhang, Baoqing He, Kaiwen Jie, Bolin Pan, Junlin Lu, Qiang Zhang, Xu Chen, Jiajian Lai
article en

Abstract

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.

Nature Communications
Sun Yat-sen University (CN), Sun Yat-sen Memorial Hospital (CN), Fifth Affiliated Hospital of Sun Yat-sen University (CN), University of Virginia (US)
Openalex Percentile: Top 27%
CRISPR and Genetic Engineering
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