Lipid Nanoparticles for <i>In Vivo</i> Lung Delivery of CRISPR-Cas9 Ribonucleoproteins Allow Gene Editing of Clinical Targets

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 <i>in vivo</i> 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 <i>in vivo</i> 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 <i>in vitro</i> gene-editing efficiency and <i>in vivo</i> 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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Publication Details

Journal
ACS Nano
Published
2025-04-04
DOI
https://doi.org/10.1021/acsnano.4c16617
Citations
13
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
10.48

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article

Lipid Nanoparticles for In Vivo Lung Delivery of CRISPR-Cas9 Ribonucleoproteins Allow Gene Editing of Clinical Targets

Christian G. Figueroa‐Espada, Alvin J. Mukalel, Hannah C. Geisler, Rebecca M. Haley et al.
13 citations
ACS Nano
CRISPR and Genetic Engineering
10.48
article

Lipid Nanoparticles for In Vivo Lung Delivery of CRISPR-Cas9 Ribonucleoproteins Allow Gene Editing of Clinical Targets

Christian G. Figueroa‐Espada, Alvin J. Mukalel, Hannah C. Geisler, Rebecca M. Haley, Beverly L. Davidson, Ryann A. Joseph, Jesse A. Weber, Michael J. Mitchell, Rakan El‐Mayta, Adele S. Ricciardi, Rohan Palanki, Marshall S. Padilla, Matthew T. Jester
article en
13 citations

Abstract

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 <i>in vivo</i> 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 <i>in vivo</i> 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 <i>in vitro</i> gene-editing efficiency and <i>in vivo</i> 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.

ACS NanoVol. 19(14)
Children's Hospital of Philadelphia (US), California University of Pennsylvania (US), Penn Center for AIDS Research (US)
Foundation for the National Institutes of Health, American Cancer Society, Burroughs Wellcome Fund, Cystic Fibrosis Foundation, University of Pennsylvania, Abramson Cancer Center, National Heart, Lung, and Blood Institute, National Cancer Institute, National Institute of Dental and Craniofacial Research, Division of Chemical, Bioengineering, Environmental, and Transport Systems, National Center for Advancing Translational Sciences
Zero hunger
Openalex Percentile: Top 1%
CRISPR and Genetic Engineering
10.48
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