Characterization of a novel conditional knockout mouse model to assess efficacy of mRNA therapy in the context of severe OTC deficiency
- PMID: 39799396
- PMCID: PMC11897776
- DOI: 10.1016/j.ymthe.2025.01.010
Characterization of a novel conditional knockout mouse model to assess efficacy of mRNA therapy in the context of severe OTC deficiency
Abstract
Ornithine transcarbamylase deficiency (OTCD) is the most common urea-cycle disorder, characterized by hyperammonemia and accompanied by a high unmet patient need. mRNA therapies have been shown to be efficacious in hypomorphic Sparse-fur abnormal skin and hair (Spf-ash) mice, a model of late-onset disease. However, studying the efficacy of ornithine transcarbamylase (OTC) mRNA therapy in traditional knockout mice, a model for severe early-onset OTCD, is hampered by the rapid lethality of the model and poor lipid nanoparticle (LNP) uptake into neonatal mouse liver. We developed a novel tamoxifen-inducible mouse to study the effect of mRNA therapy in the context of complete or near-complete OTC loss in adult animals. Characterization of the model showed that it is highly reproducible, 100% penetrant, and phenocopies hallmarks of human disease, with animals exhibiting decreased body weight, hyperammonemia, and brain edema. Delivery of OTC mRNA increased survival, maintained body weight, delayed the onset of hyperammonemia, and reduced brain edema. Therefore, this model provides a platform to study LNP-mediated mRNA therapies for the treatment of late-onset OTCD.
Keywords: LNP-mediated delivery; OTC; OTCD; conditional knockout; mRNA therapy; mouse model; ornithine transcarbamylase deficiency.
Copyright © 2025 The American Society of Gene and Cell Therapy. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of interests J.Z., S.L., L.Y., A.F., A.-R.G., M.P., M.S., S.N., M.Z., and P.F.F. are employees and shareholders of Moderna, Inc. R.W., T.P., E.J., and P.G.V.M. are former employees of Moderna, Inc.
References
-
- Tuchman M., Lee B., Lichter-Konecki U., Summar M.L., Yudkoff M., Cederbaum S.D., Kerr D.S., Diaz G.A., Seashore M.R., Lee H.-S., et al. Cross-sectional multicenter study of patients with urea cycle disorders in the United States. Mol. Genet. Metab. 2008;94:397–402. doi: 10.1016/j.ymgme.2008.05.004. - DOI - PMC - PubMed
-
- Summar M.L., Koelker S., Freedenberg D., Le Mons C., Haberle J., Lee H.-S., Kirmse B., European Registry and Network for Intoxication Type Metabolic Diseases. Members of the Urea Cycle Disorders Consortium The incidence of urea cycle disorders. Mol. Genet. Metab. 2013;110:179–180. doi: 10.1016/j.ymgme.2013.07.008. - DOI - PMC - PubMed
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