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Application of Antisense Conjugates for the Treatment of Myotonic Dystrophy Type 1.
Stoodley, Jessica; Vallejo-Bedia, Francisco; Seone-Miraz, David; Debasa-Mouce, Manuel; Wood, Matthew J A; Varela, Miguel A.
Afiliación
  • Stoodley J; Department of Paediatrics, Institute of Developmental and Regenerative Medicine (IDRM), University of Oxford, Roosevelt Dr, Oxford OX3 7TY, UK.
  • Vallejo-Bedia F; MDUK Oxford Neuromuscular Centre, Oxford OX3 7TY, UK.
  • Seone-Miraz D; Department of Paediatrics, Institute of Developmental and Regenerative Medicine (IDRM), University of Oxford, Roosevelt Dr, Oxford OX3 7TY, UK.
  • Debasa-Mouce M; MDUK Oxford Neuromuscular Centre, Oxford OX3 7TY, UK.
  • Wood MJA; Department of Paediatrics, Institute of Developmental and Regenerative Medicine (IDRM), University of Oxford, Roosevelt Dr, Oxford OX3 7TY, UK.
  • Varela MA; MDUK Oxford Neuromuscular Centre, Oxford OX3 7TY, UK.
Int J Mol Sci ; 24(3)2023 Jan 31.
Article en En | MEDLINE | ID: mdl-36769018
Myotonic dystrophy type 1 (DM1) is one of the most common muscular dystrophies and can be potentially treated with antisense therapy decreasing mutant DMPK, targeting miRNAs or their binding sites or via a blocking mechanism for MBNL1 displacement from the repeats. Unconjugated antisense molecules are able to correct the disease phenotype in mouse models, but they show poor muscle penetration upon systemic delivery in DM1 patients. In order to overcome this challenge, research has focused on the improvement of the therapeutic window and biodistribution of antisense therapy using bioconjugation to lipids, cell penetrating peptides or antibodies. Antisense conjugates are able to induce the long-lasting correction of DM1 pathology at both molecular and functional levels and also efficiently penetrate hard-to-reach tissues such as cardiac muscle. Delivery to the CNS at clinically relevant levels remains challenging and the use of alternative administration routes may be necessary to ameliorate some of the symptoms experienced by DM1 patients. With several antisense therapies currently in clinical trials, the outlook for achieving a clinically approved treatment for patients has never looked more promising.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Distrofias Musculares / Distrofia Miotónica Límite: Animals Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Distrofias Musculares / Distrofia Miotónica Límite: Animals Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article Pais de publicación: Suiza