Toward Next-Gen Cell Therapy for Pediatric Patients: Neonatal Hepatocytes Tolerate Electroporation-Mediated Gene Editing and Engraft in the Liver
. Quantitative histological analysis revealed comparable liver repopulation levels between recipients of gene-edited neonatal cells and adult cells after hepatoxicity-mediated selection, providing a benchmark for electroporation-mediated gene editing in neonatal hepatocytes, and supporting the development of genetically corrected neonatal hepatocyte products as a crucial long-term or bridge-to-transplant therapeutic strategy for pediatric liver disease.
Authors
- Abishek Dhungana
- Olumide Adebayo (ORCID: https://orcid.org/0000-0001-5163-3498)
- Renee N. Cottle (ORCID: https://orcid.org/0000-0002-7971-2865)
- Menam Pokhrel (ORCID: https://orcid.org/0000-0002-8602-2256)
- J. Mark Gibson
- Benjamin Bessah Arthur
- Daniel Hossack
Institutions
- Greenwood Genetic Center (US)
- Clemson University (US)
Publication Details
- Journal
- The CRISPR Journal
- Published
- 2026-04-01
- DOI
- https://doi.org/10.1177/25731599261430830
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 0.00