In Vivo Efficacy and Safety Evaluations of Therapeutic Splicing Correction Using U1 snRNA in the Mouse Retina.
Sebastian SwirskiOliver MayMalte AhlersBernd WissingerMartin GreschnerChristoph JüschkeJohn NeidhardtPublished in: Cells (2023)
Efficacy and safety considerations constitute essential steps during development of in vivo gene therapies. Herein, we evaluated efficacy and safety of splice factor-based treatments to correct mutation-induced splice defects in an Opa1 mutant mouse line. We applied adeno-associated viruses to the retina. The viruses transduced retinal cells with an engineered U1 snRNA splice factor designed to correct the Opa1 splice defect. We found the treatment to be efficient in increasing wild-type Opa1 transcripts. Correspondingly, Opa1 protein levels increased significantly in treated eyes. Measurements of retinal morphology and function did not reveal therapy-related side-effects supporting the short-term safety of the treatment. Alterations of potential off-target genes were not detected. Our data suggest that treatments of splice defects applying engineered U1 snRNAs represent a promising in vivo therapeutic approach. The therapy increased wild-type Opa1 transcripts and protein levels without detectable morphological, functional or genetic side-effects in the mouse eye. The U1 snRNA-based therapy can be tailored to specific disease gene mutations, hence, raising the possibility of a wider applicability of this promising technology towards treatment of different inherited retinal diseases.
Keyphrases
- wild type
- diabetic retinopathy
- optical coherence tomography
- genome wide
- gene expression
- copy number
- electronic health record
- combination therapy
- machine learning
- dna methylation
- stem cells
- mesenchymal stem cells
- replacement therapy
- big data
- protein protein
- cell death
- transcription factor
- oxidative stress
- newly diagnosed
- soft tissue
- genetic diversity