| Literature DB >> 34808387 |
Margherita Bersani1, Mafalda Rizzuti2, Elisa Pagliari1, Manuela Garbellini3, Domenica Saccomanno2, Hong M Moulton4, Nereo Bresolin5, Giacomo P Comi6, Stefania Corti5, Monica Nizzardo7.
Abstract
Spinal muscular atrophy (SMA) is a motor neuron disease and the leading genetic cause of infant mortality. Recently approved SMA therapies have transformed a deadly disease into a survivable one, but these compounds show a wide spectrum of clinical response and effective rescue only in the early stages of the disease. Therefore, safe, symptomatic-suitable, non-invasive treatments with high clinical impact across different phenotypes are urgently needed. We conjugated antisense oligonucleotides with Morpholino (MO) chemistry, which increase SMN protein levels, to cell-penetrating peptides (CPPs) for better cellular distribution. Systemically administered MOs linked to r6 and (RXRRBR)2XB peptides crossed the blood-brain barrier and increased SMN protein levels remarkably, causing striking improvement of survival, neuromuscular function, and neuropathology, even in symptomatic SMA animals. Our study demonstrates that MO-CPP conjugates can significantly expand the therapeutic window through minimally invasive systemic administration, opening the path for clinical applications of this strategy.Entities:
Keywords: antisense oligonucleotides; cell-penetrating peptides; spinal muscular atrophy; symptomatic treatment; systemic treatment
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Year: 2021 PMID: 34808387 PMCID: PMC8899506 DOI: 10.1016/j.ymthe.2021.11.012
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454