Curative levels of endogenous gene replacement achieved in non-human primate liver using programmable genomic integration
Jenny XieiD, Maike Thamsen Dunyak, Patrick HannaiD, Angela Xinyi Nan, Brett EstesiD, Jesse C. CochraneiD, Shuai WuiD, Jie WangiD, Connor McGinnis, Qiang WangiD, Rejina Pokharel, Dev PaudeliD, Jason ZhangiD, Dan LiiD, Parth H. Amin, Siddharth Narayan, Angela Hsia, Dane Z. HazelbakeriD, Xiarong Shi, Meredith Packer, Brian R. DukeiD, Ryan Dickerson, Charlotte PiardiD, Martin MeagheriD, Jason T. Gatlin, , Jonathan D. FinniD
Abstract
The ability to efficiently place a large piece of DNA in a specific genomic location has been a goal for the gene therapy field since its inception; however, despite significant advances in gene editing technology, this had yet to be achieved. Here we describe two methods of programmable genomic integration (PGI) that overcome some of the limitations of current approaches. Using a combination of clinically validated delivery technologies (LNP, AAV), we demonstrate the ability to specifically integrate large (>2 kb) DNA sequences into endogenous introns in the liver of non-human primates (NHP). PGI was effective across multiple genomic locations and transgenes, and insertion led to expression from the endogenous promoter. PGI was highly efficient, achieving expression in >50% of liver cells after a single course of treatment, which would be curative for most monogenic recessive liver diseases. This is the first report of clinically curative level of gene insertion at endogenous loci in NHP.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 6
- Organism
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Loss of transgene expression limits liver gene therapy in primates
Jenny A. Greig, Kelly M. Martins, … James M. Wilson·Nature BiotechnologyPeer-reviewed·Nov 6, 2023
- Treatment of a genetic liver disease in mice through transient prime editor expression
Tanja Rothgangl, András Tálas, … Gerald Schwank·Nature Biomedical EngineeringPeer-reviewed·May 20, 2025
- Therapeutic Knock-in Genome Editing Using Single AAV Vectors in Mouse Models of Inherited Liver Disease
Khishigjargal Batjargal, Tomoki Togashi, … Tsukasa Ohmori·bioRxiv·Jul 30, 2025
- Breaking Free: Development of Circular AAV Cargos for Targeted Seamless Integration in the Liver
Brett Estes, Nisha Gandhi, … Jenny Xie·Molecular Therapy — Methods & Clinical DevelopmentPeer-reviewed·May 14, 2025
- Low RT-based Genome Editing Fidelity in Mouse Hepatocytes: Challenges and Solutions
Maike Thamsen Dunyak, Patrick Hanna, … Jonathan D. Finn·bioRxiv·Oct 31, 2024
- Drag-and-drop genome insertion without DNA cleavage with CRISPR-directed integrases
E. I. Ioannidi, M. T. N. Yarnall, … O. O. Abudayyeh·bioRxiv·Nov 1, 2021