Systemic delivery of full-length dystrophin in Duchenne muscular dystrophy mice
Yuan Zhou,
Chen Zhang,
Weidong Xiao,
Roland W. Herzog and
Renzhi Han ()
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Yuan Zhou: Indiana University School of Medicine
Chen Zhang: Indiana University School of Medicine
Weidong Xiao: Indiana University School of Medicine
Roland W. Herzog: Indiana University School of Medicine
Renzhi Han: Indiana University School of Medicine
Nature Communications, 2024, vol. 15, issue 1, 1-14
Abstract:
Abstract Current gene therapy for Duchenne muscular dystrophy (DMD) utilizes adeno-associated virus (AAV) to deliver micro-dystrophin (µDys), which does not provide full protection for striated muscles as it lacks many important functional domains of full-length (FL) dystrophin. Here we develop a triple vector system to deliver FL-dystrophin into skeletal and cardiac muscles. We split FL-dystrophin into three fragments linked to two orthogonal pairs of split intein, allowing efficient assembly of FL-dystrophin. The three fragments packaged in myotropic AAV (MyoAAV4A) restore FL-dystrophin expression in both skeletal and cardiac muscles in male mdx4cv mice. Dystrophin-glycoprotein complex components are also restored at the sarcolemma of dystrophic muscles. MyoAAV4A-delivered FL-dystrophin significantly improves muscle histopathology, contractility, and overall strength comparable to µDys, but unlike µDys, it also restores defective cavin 4 localization and associated signaling in mdx4cv heart. Therefore, our data support the feasibility of a mutation-independent FL-dystrophin gene therapy for DMD, warranting further clinical development.
Date: 2024
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DOI: 10.1038/s41467-024-50569-6
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