QR-1011 restores defective ABCA4 splicing caused by multiple severe ABCA4 variants underlying Stargardt disease

• Published in: Scientific reports Vol. 14; no. 1; p. 684
• Main Authors: Kaltak, Melita, de Bruijn, Petra, van Leeuwen, Willemijn, Platenburg, Gerard, Cremers, Frans P. M., Collin, Rob W. J., Swildens, Jim
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 06.01.2024; Nature Publishing Group; Nature Portfolio
• Subjects: 631/208/1792; 631/61/201; 631/61/2299; Antisense oligonucleotides; Disease; Dystrophy; Epithelium; Humanities and Social Sciences; Metabolites; multidisciplinary; Mutation; Organoids; Photoreceptors; Proteins; Retina; Retinal pigment epithelium; Science; Science (multidisciplinary); Splicing
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-51203-7

Stargardt disease type 1 (STGD1), the most common form of hereditary macular dystrophy, can be caused by biallelic combinations of over 2200 variants in the ABCA4 gene. This leads to reduced or absent ABCA4 protein activity, resulting in toxic metabolite accumulation in the retina and damage of the retinal pigment epithelium and photoreceptors. Approximately 21% of all ABCA4 variants that contribute to disease influence ABCA4 pre-mRNA splicing. This emphasizes the need for therapies to restore disrupted ABCA4 splicing and halt STGD1 progression. Previously, QR-1011, an antisense oligonucleotide (AON), successfully corrected splicing abnormalities and restored normal ABCA4 protein translation in human retinal organoids carrying the prevalent disease-causing variant c.5461−10T>C in ABCA4 . Here, we investigated whether QR-1011 could also correct splicing in four less common non-canonical splice site (NCSS) variants flanking ABCA4  exon 39: c.5461−8T>G, c.5461−6T>C, c.5584+5G>A and c.5584+6T>C. We administered QR-1011 and three other AONs to midigene-transfected cells and demonstrate that QR-1011 had the most pronounced effect on splicing compared to the others. Moreover, QR-1011 significantly increased full-length ABCA4 transcript levels for c.5461−8T>G and c.5584+6T>C. Splicing restoration could not be achieved in the other two variants, suggesting their more severe effect on splicing. Overall, QR-1011, initially developed for a single ABCA4 variant, exhibited potent splice correction capabilities for two additional severe NCSS variants nearby. This suggests the possibility of a broader therapeutic impact of QR-1011 extending beyond its original target and highlights the potential for treating a larger population of STGD1 patients affected by multiple severe ABCA4 variants with a single AON.