In vivo correction of cystic fibrosis mediated by PNA nanoparticles

Author:

Piotrowski-Daspit Alexandra S.1ORCID,Barone Christina2,Lin Chun-Yu1,Deng Yanxiang1ORCID,Wu Douglas1,Binns Thomas C.13ORCID,Xu Emily4ORCID,Ricciardi Adele S.1ORCID,Putman Rachael1ORCID,Garrison Alannah2ORCID,Nguyen Richard2,Gupta Anisha5ORCID,Fan Rong1ORCID,Glazer Peter M.56ORCID,Saltzman W. Mark178ORCID,Egan Marie E.28ORCID

Affiliation:

1. Department of Biomedical Engineering, Yale University, New Haven, CT 06511, USA.

2. Department of Pediatrics, Yale School of Medicine, New Haven, CT 06520, USA.

3. Department of Laboratory Medicine, Yale School of Medicine, New Haven, CT 06520, USA.

4. Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06511, USA.

5. Department of Therapeutic Radiology, Yale School of Medicine, New Haven, CT 06520, USA.

6. Department of Genetics, Yale School of Medicine, New Haven, CT 06520, USA.

7. Department of Chemical and Environmental Engineering, Yale University, New Haven, CT 06511, USA.

8. Department of Cellular and Molecular Physiology, Yale School of Medicine, New Haven, CT 06520, USA.

Abstract

Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene. We sought to correct the multiple organ dysfunction of the F508del CF-causing mutation using systemic delivery of peptide nucleic acid gene editing technology mediated by biocompatible polymeric nanoparticles. We confirmed phenotypic and genotypic modification in vitro in primary nasal epithelial cells from F508del mice grown at air-liquid interface and in vivo in F508del mice following intravenous delivery. In vivo treatment resulted in a partial gain of CFTR function in epithelia as measured by in situ potential differences and Ussing chamber assays and correction of CFTR in both airway and GI tissues with no off-target effects above background. Our studies demonstrate that systemic gene editing is possible, and more specifically that intravenous delivery of PNA NPs designed to correct CF-causing mutations is a viable option to ameliorate CF in multiple affected organs.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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