Literature DB >> 30448197

Efficacy of Multi-exon Skipping Treatment in Duchenne Muscular Dystrophy Dog Model Neonates.

Kenji Rowel Q Lim1, Yusuke Echigoya2, Tetsuya Nagata3, Mutsuki Kuraoka3, Masanori Kobayashi4, Yoshitsugu Aoki3, Terence Partridge5, Rika Maruyama1, Shin'ichi Takeda6, Toshifumi Yokota7.   

Abstract

Duchenne muscular dystrophy (DMD) is caused by mutations in DMD, which codes for dystrophin. Because the progressive and irreversible degeneration of muscle occurs from childhood, earlier therapy is required to prevent dystrophic progression. Exon skipping by antisense oligonucleotides called phosphorodiamidate morpholino oligomers (PMOs), which restores the DMD reading frame and dystrophin expression, is a promising candidate for use in neonatal patients, yet the potential remains unclear. Here, we investigate the systemic efficacy and safety of early exon skipping in dystrophic dog neonates. Intravenous treatment of canine X-linked muscular dystrophy in Japan dogs with a 4-PMO cocktail resulted in ∼3%-27% in-frame exon 6-9 skipping and dystrophin restoration across skeletal muscles up to 14% of healthy levels. Histopathology was ameliorated with the reduction of fibrosis and/or necrosis area and centrally nucleated fibers, significantly in the diaphragm. Treatment induced cardiac multi-exon skipping, though dystrophin rescue was not detected. Functionally, treatment led to significant improvement in the standing test. Toxicity was not observed from blood tests. This is the first study to demonstrate successful multi-exon skipping treatment and significant functional improvement in dystrophic dogs. Early treatment was most beneficial for respiratory muscles, with implications for addressing pulmonary malfunction in patients.
Copyright © 2018 The American Society of Gene and Cell Therapy. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Becker muscular dystrophy; Duchenne muscular dystrophy; antisense therapy; dystrophin restoration; early exon skipping treatment; exon 6-8 skipping; morpholinos; multiple exon skipping; neonatal dystrophic dogs; systemic treatment

Mesh:

Substances:

Year:  2018        PMID: 30448197      PMCID: PMC6318815          DOI: 10.1016/j.ymthe.2018.10.011

Source DB:  PubMed          Journal:  Mol Ther        ISSN: 1525-0016            Impact factor:   11.454


  50 in total

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Authors:  Judith C T van Deutekom; Gert-Jan B van Ommen
Journal:  Nat Rev Genet       Date:  2003-10       Impact factor: 53.242

2.  Stability of cell-penetrating peptide-morpholino oligomer conjugates in human serum and in cells.

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Journal:  Bioconjug Chem       Date:  2007 Jan-Feb       Impact factor: 4.774

Review 3.  The delivery of therapeutic oligonucleotides.

Authors:  Rudolph L Juliano
Journal:  Nucleic Acids Res       Date:  2016-04-15       Impact factor: 16.971

4.  Antisense PMO found in dystrophic dog model was effective in cells from exon 7-deleted DMD patient.

Authors:  Takashi Saito; Akinori Nakamura; Yoshitsugu Aoki; Toshifumi Yokota; Takashi Okada; Makiko Osawa; Shin'ichi Takeda
Journal:  PLoS One       Date:  2010-08-18       Impact factor: 3.240

5.  Major clinical and histopathological characteristics of canine X-linked muscular dystrophy in Japan, CXMDJ.

Authors:  Yoshiki Shimatsu; Madoka Yoshimura; Katsutoshi Yuasa; Nobuyuki Urasawa; Masayuki Tomohiro; Masao Nakura; Manabu Tanigawa; Akinori Nakamura; Shin'ichi Takeda
Journal:  Acta Myol       Date:  2005-10

6.  Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-year follow-up.

Authors:  Luciano Merlini; Monia Gennari; Elisabetta Malaspina; Ilaria Cecconi; Annarita Armaroli; Saverio Gnudi; Beril Talim; Alessandra Ferlini; Alessandro Cicognani; Emilio Franzoni
Journal:  Muscle Nerve       Date:  2012-06       Impact factor: 3.217

7.  Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse.

Authors:  C J Mann; K Honeyman; A J Cheng; T Ly; F Lloyd; S Fletcher; J E Morgan; T A Partridge; S D Wilton
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-02       Impact factor: 11.205

8.  Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin-α2 chain-null congenital muscular dystrophy mice.

Authors:  Yoshitsugu Aoki; Tetsuya Nagata; Toshifumi Yokota; Akinori Nakamura; Matthew J A Wood; Terence Partridge; Shin'ichi Takeda
Journal:  Hum Mol Genet       Date:  2013-07-23       Impact factor: 6.150

9.  Cellular trafficking determines the exon skipping activity of Pip6a-PMO in mdx skeletal and cardiac muscle cells.

Authors:  Taavi Lehto; Alejandra Castillo Alvarez; Sarah Gauck; Michael J Gait; Thibault Coursindel; Matthew J A Wood; Bernard Lebleu; Prisca Boisguerin
Journal:  Nucleic Acids Res       Date:  2013-12-23       Impact factor: 16.971

Review 10.  Current and emerging treatment strategies for Duchenne muscular dystrophy.

Authors:  Jean K Mah
Journal:  Neuropsychiatr Dis Treat       Date:  2016-07-22       Impact factor: 2.570

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  8 in total

1.  Exons 45-55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD Gene.

Authors:  Yusuke Echigoya; Kenji Rowel Q Lim; Dyanna Melo; Bo Bao; Nhu Trieu; Yoshitaka Mizobe; Rika Maruyama; Kamel Mamchaoui; Jun Tanihata; Yoshitsugu Aoki; Shin'ichi Takeda; Vincent Mouly; William Duddy; Toshifumi Yokota
Journal:  Mol Ther       Date:  2019-07-26       Impact factor: 11.454

2.  Antisense Oligonucleotide Treatment in a Humanized Mouse Model of Duchenne Muscular Dystrophy and Highly Sensitive Detection of Dystrophin Using Western Blotting.

Authors:  Rika Maruyama; Toshifumi Yokota
Journal:  Methods Mol Biol       Date:  2021

Review 3.  Pharmacology and toxicology of eteplirsen and SRP-5051 for DMD exon 51 skipping: an update.

Authors:  Omar Sheikh; Toshifumi Yokota
Journal:  Arch Toxicol       Date:  2021-11-19       Impact factor: 5.153

Review 4.  Restoring Protein Expression in Neuromuscular Conditions: A Review Assessing the Current State of Exon Skipping/Inclusion and Gene Therapies for Duchenne Muscular Dystrophy and Spinal Muscular Atrophy.

Authors:  Omar Sheikh; Toshifumi Yokota
Journal:  BioDrugs       Date:  2021-06-07       Impact factor: 5.807

5.  A Genotype-Phenotype Correlation Study of Exon Skip-Equivalent In-Frame Deletions and Exon Skip-Amenable Out-of-Frame Deletions across the DMD Gene to Simulate the Effects of Exon-Skipping Therapies: A Meta-Analysis.

Authors:  Saeed Anwar; Merry He; Kenji Rowel Q Lim; Rika Maruyama; Toshifumi Yokota
Journal:  J Pers Med       Date:  2021-01-14

6.  Development of DG9 peptide-conjugated single- and multi-exon skipping therapies for the treatment of Duchenne muscular dystrophy.

Authors:  Kenji Rowel Q Lim; Stanley Woo; Dyanna Melo; Yiqing Huang; Kasia Dzierlega; Md Nur Ahad Shah; Tejal Aslesh; Rohini Roy Roshmi; Yusuke Echigoya; Rika Maruyama; Hong M Moulton; Toshifumi Yokota
Journal:  Proc Natl Acad Sci U S A       Date:  2022-03-01       Impact factor: 12.779

7.  A gene-edited mouse model of limb-girdle muscular dystrophy 2C for testing exon skipping.

Authors:  Alexis R Demonbreun; Eugene J Wyatt; Katherine S Fallon; Claire C Oosterbaan; Patrick G Page; Michele Hadhazy; Mattia Quattrocelli; David Y Barefield; Elizabeth M McNally
Journal:  Dis Model Mech       Date:  2019-11-04       Impact factor: 5.758

Review 8.  Evaluating the potential of novel genetic approaches for the treatment of Duchenne muscular dystrophy.

Authors:  Vratko Himič; Kay E Davies
Journal:  Eur J Hum Genet       Date:  2021-02-09       Impact factor: 4.246

  8 in total

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