TANGO With SCN1A: Can This Molecular Dance Defeat Dravet Syndrome?

Antisense Oligonucleotides Increase Scn1a Expression and Reduce Seizures and SUDEP Incidence in a Mouse Model of Dravet Syndrome Han Z, Chen C, Christiansen A, et al. Sci Transl Med. 2020;12(558):eaaz6100. doi: PMID:32848094. Dravet syndrome (DS) is an intractable developmental and epileptic encephalopathy caused largely by de novo variants in the SCN1A gene, resulting in haploinsufficiency of the voltage-gated sodium channel alpha subunit Na(V)1.1. Here, we used Targeted Augmentation of Nuclear Gene Output (TANGO) technology, which modulates naturally occurring, nonproductive splicing events to increase target gene and protein expression and ameliorate disease phenotype in a mouse model. We identified antisense oligonucleotides (ASOs) that specifically increase the expression of productive Scn1a transcript in human cell lines, as well as in mouse brain. We show that a single intracerebroventricular dose of a lead ASO at postnatal day 2 or 14 reduced the incidence of electrographic seizures and sudden unexpected death in epilepsy in the F1:129S-Scn1a(+/-) x C57BL/6J mouse model of DS. Increased expression of productive Scn1a transcript and Na(V)1.1 protein was confirmed in brains of treated mice. Our results suggest that TANGO may provide a unique, gene-specific approach for the treatment of DS.

Automated summary

The study utilized TANGO technology to increase the expression of the Scn1a gene and found that antisense oligonucleotides reduced seizures and sudden unexpected death in a mouse model of Dravet syndrome. This research provides a potential gene-specific approach for the treatment of DS.