Literature DB >> 31591596

Non-immunogenic utrophin gene therapy for the treatment of muscular dystrophy animal models.

Yafeng Song1, Leon Morales1, Alock S Malik1, Andrew F Mead1, Christopher D Greer1, Marilyn A Mitchell1, Mihail T Petrov1, Leonard T Su1, Margaret E Choi1, Shira T Rosenblum1, Xiangping Lu1, Daniel J VanBelzen1, Ranjith K Krishnankutty1, Frederick J Balzer1, Emanuele Loro2, Robert French1, Kathleen J Propert3, Shangzhen Zhou4, Benjamin W Kozyak1,5, Peter P Nghiem6, Tejvir S Khurana2, Joe N Kornegay6, Hansell H Stedman7,8.   

Abstract

The essential product of the Duchenne muscular dystrophy (DMD) gene is dystrophin1, a rod-like protein2 that protects striated myocytes from contraction-induced injury3,4. Dystrophin-related protein (or utrophin) retains most of the structural and protein binding elements of dystrophin5. Importantly, normal thymic expression in DMD patients6 should protect utrophin by central immunologic tolerance. We designed a codon-optimized, synthetic transgene encoding a miniaturized utrophin (µUtro), deliverable by adeno-associated virus (AAV) vectors. Here, we show that µUtro is a highly functional, non-immunogenic substitute for dystrophin, preventing the most deleterious histological and physiological aspects of muscular dystrophy in small and large animal models. Following systemic administration of an AAV-µUtro to neonatal dystrophin-deficient mdx mice, histological and biochemical markers of myonecrosis and regeneration are completely suppressed throughout growth to adult weight. In the dystrophin-deficient golden retriever model, µUtro non-toxically prevented myonecrosis, even in the most powerful muscles. In a stringent test of immunogenicity, focal expression of µUtro in the deletional-null German shorthaired pointer model produced no evidence of cell-mediated immunity, in contrast to the robust T cell response against similarly constructed µDystrophin (µDystro). These findings support a model in which utrophin-derived therapies might be used to treat clinical dystrophin deficiency, with a favorable immunologic profile and preserved function in the face of extreme miniaturization.

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Year:  2019        PMID: 31591596      PMCID: PMC7274039          DOI: 10.1038/s41591-019-0594-0

Source DB:  PubMed          Journal:  Nat Med        ISSN: 1078-8956            Impact factor:   53.440


  1 in total

1.  In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes.

Authors:  P R Clemens; S Kochanek; Y Sunada; S Chan; H H Chen; K P Campbell; C T Caskey
Journal:  Gene Ther       Date:  1996-11       Impact factor: 5.250

  1 in total
  27 in total

Review 1.  Correction of muscular dystrophies by CRISPR gene editing.

Authors:  Francesco Chemello; Rhonda Bassel-Duby; Eric N Olson
Journal:  J Clin Invest       Date:  2020-06-01       Impact factor: 14.808

2.  Micro-utrophin Therapy for Duchenne Muscular Dystrophy.

Authors:  Dongsheng Duan
Journal:  Mol Ther       Date:  2019-10-22       Impact factor: 11.454

3.  Validation of DE50-MD dogs as a model for the brain phenotype of Duchenne muscular dystrophy.

Authors:  Abbe H Crawford; John C W Hildyard; Sophie A M Rushing; Dominic J Wells; Maria Diez-Leon; Richard J Piercy
Journal:  Dis Model Mech       Date:  2022-03-02       Impact factor: 5.758

4.  Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation.

Authors:  G Diane Shelton; Katie M Minor; Ling T Guo; Steven G Friedenberg; Jonah N Cullen; Jeffrey M Hord; David Venzke; Mary E Anderson; Megan Devereaux; Sally J Prouty; Caryl Handelman; Kevin P Campbell; James R Mickelson
Journal:  Neuromuscul Disord       Date:  2021-07-28       Impact factor: 4.296

5.  Multifunctional Natural Polymer Nanoparticles as Antifibrotic Gene Carriers for CKD Therapy.

Authors:  Adam C Midgley; Yongzhen Wei; Dashuai Zhu; Fangli Gao; Hongyu Yan; Anila Khalique; Wenya Luo; Huan Jiang; Xiangsheng Liu; Jiasen Guo; Chuangnian Zhang; Guowei Feng; Kai Wang; Xueyuan Bai; Wen Ning; Chao Yang; Qiang Zhao; Deling Kong
Journal:  J Am Soc Nephrol       Date:  2020-08-07       Impact factor: 10.121

Review 6.  Modulating gene regulation to treat genetic disorders.

Authors:  Navneet Matharu; Nadav Ahituv
Journal:  Nat Rev Drug Discov       Date:  2020-10-05       Impact factor: 84.694

7.  Functional enhancer elements drive subclass-selective expression from mouse to primate neocortex.

Authors:  John K Mich; Lucas T Graybuck; Erik E Hess; Joseph T Mahoney; Yoshiko Kojima; Yi Ding; Saroja Somasundaram; Jeremy A Miller; Brian E Kalmbach; Cristina Radaelli; Bryan B Gore; Natalie Weed; Victoria Omstead; Yemeserach Bishaw; Nadiya V Shapovalova; Refugio A Martinez; Olivia Fong; Shenqin Yao; Marty Mortrud; Peter Chong; Luke Loftus; Darren Bertagnolli; Jeff Goldy; Tamara Casper; Nick Dee; Ximena Opitz-Araya; Ali Cetin; Kimberly A Smith; Ryder P Gwinn; Charles Cobbs; Andrew L Ko; Jeffrey G Ojemann; C Dirk Keene; Daniel L Silbergeld; Susan M Sunkin; Viviana Gradinaru; Gregory D Horwitz; Hongkui Zeng; Bosiljka Tasic; Ed S Lein; Jonathan T Ting; Boaz P Levi
Journal:  Cell Rep       Date:  2021-03-30       Impact factor: 9.423

Review 8.  U7 snRNA: A tool for gene therapy.

Authors:  Ankur Gadgil; Katarzyna Dorota Raczyńska
Journal:  J Gene Med       Date:  2021-02-23       Impact factor: 4.565

Review 9.  Visceral myopathy: clinical syndromes, genetics, pathophysiology, and fall of the cytoskeleton.

Authors:  Sohaib Khalid Hashmi; Rachel Helen Ceron; Robert O Heuckeroth
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2021-03-17       Impact factor: 4.871

Review 10.  Challenges at the Crossroads: Myopathy Trials in 2020 Hindsight.

Authors:  Christopher Greer; Benjamin Kozyak; Hansell Stedman
Journal:  Mol Ther       Date:  2021-01-14       Impact factor: 11.454

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