Why the study?
Significant delivery barriers remain for CRISPR-Cas9 application in the clinic, particularly for in vivo and extrahepatic applications.
A novel lung-tropic lipid nanoparticle enables highly specific in vivo CRISPR-Cas9 gene editing in lung tissue without hepatic off-target effects, advancing extrahepatic gene therapy delivery.
Lung-tropic LNPs achieved efficient CRISPR editing in murine lungs without hepatic off-targets; leaves open translation to human extrahepatic applications.
In the past 10 years, CRISPR-Cas9 has revolutionized the gene-editing field due to its modularity, simplicity, and efficacy. It has been applied for the creation of in vivo models, to further understand human biology, and toward the curing of genetic diseases. However, there remain significant delivery barriers for CRISPR-Cas9 application in the clinic, especially for in vivo and extrahepatic applications. In this work, high-throughput molecular barcoding techniques were used alongside traditional screening methodologies to simultaneously evaluate LNP formulations encapsulating ribonucleoproteins (RNPs) for in vitro gene-editing efficiency and in vivo biodistribution. This resulted in the identification of a lung-tropic LNP formulation, which shows efficient gene editing in endothelial and epithelial cells within the lung, targeting both model reporter and clinically relevant genomic targets. Further, this LNP shows no off-target indel formation in the liver, making it a highly specific extrahepatic delivery system for lung-editing applications.
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Haley et al. (2025) studied this question.
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