دورية أكاديمية

Micro-dystrophin gene therapy demonstrates long-term cardiac efficacy in a severe Duchenne muscular dystrophy model

التفاصيل البيبلوغرافية
العنوان: Micro-dystrophin gene therapy demonstrates long-term cardiac efficacy in a severe Duchenne muscular dystrophy model
المؤلفون: Arden B. Piepho, Jeovanna Lowe, Laurel R. Cumby, Lisa E. Dorn, Dana M. Lake, Neha Rastogi, Megan D. Gertzen, Sarah L. Sturgill, Guy L. Odom, Mark T. Ziolo, Federica Accornero, Jeffrey S. Chamberlain, Jill A. Rafael-Fortney
المصدر: Molecular Therapy: Methods & Clinical Development, Vol 28, Iss , Pp 344-354 (2023)
بيانات النشر: Elsevier, 2023.
سنة النشر: 2023
المجموعة: LCC:Genetics
LCC:Cytology
مصطلحات موضوعية: muscular dystrophy, cardiomyopathy, gene therapy, fibrosis, DMD, utrophin, Genetics, QH426-470, Cytology, QH573-671
الوصف: Micro-dystrophin gene replacement therapies for Duchenne muscular dystrophy (DMD) are currently in clinical trials, but have not been thoroughly investigated for their efficacy on cardiomyopathy progression to heart failure. We previously validated Fiona/dystrophin-utrophin-deficient (dko) mice as a DMD cardiomyopathy model that progresses to reduced ejection fraction indicative of heart failure. Adeno-associated viral (AAV) vector delivery of an early generation micro-dystrophin prevented cardiac pathology and functional decline through 1 year of age in this new model. We now show that gene therapy using a micro-dystrophin optimized for skeletal muscle efficacy (AAV-μDys5), and which is currently in a clinical trial, is able to fully prevent cardiac pathology and cardiac strain abnormalities and maintain normal (>45%) ejection fraction through 18 months of age in Fiona/dko mice. Early treatment with AAV-μDys5 prevents inflammation and fibrosis in Fiona/dko hearts. Collagen in cardiac fibrotic scars becomes more tightly packed from 12 to 18 months in Fiona/dko mice, but the area of fibrosis containing tenascin C does not change. Increased tight collagen correlates with unexpected improvements in Fiona/dko whole-heart function that maintain impaired cardiac strain and strain rate. This study supports micro-dystrophin gene therapy as a promising intervention for preventing DMD cardiomyopathy progression.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2329-0501
العلاقة: http://www.sciencedirect.com/science/article/pii/S2329050123000116Test; https://doaj.org/toc/2329-0501Test
DOI: 10.1016/j.omtm.2023.02.001
الوصول الحر: https://doaj.org/article/112376132c914e0588ee19091b2c6a91Test
رقم الانضمام: edsdoj.112376132c914e0588ee19091b2c6a91
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23290501
DOI:10.1016/j.omtm.2023.02.001