Gene Therapy for Duchenne Muscular Dystrophy

A gene therapy clinical trial may open up new possibilities for the treatment of Duchenne muscular dystrophy. Pictured: A conceptual illustration of a DNA helix.

Published in NeuroLogic - NeuroLogic Winter 2021

Though long-established treatments for Duchenne muscular dystrophy (DMD), such as corticosteroids, and newer treatments, such as exon-skipping therapies, can extend the time it takes for the disease’s grim symptoms to take hold, no available therapy can halt the condition’s progression, or — more optimistically — reverse it, explains Johns Hopkins neurologist Jessica Nance.

However, a clinical trial taking place soon at Johns Hopkins may have potential to bring this lofty goal to fruition, by using gene therapy to help repair the source of disease.


Nance explains that DMD is caused by deletions, duplications, point mutations or premature stop codons in the gene that makes dystrophin, a protein that stabilizes muscle cell membranes and supports the contractile apparatus. Without this protein, damage builds up over time, leading to muscle scarring, inflammation and eventually atrophy. Boys with this X-linked condition often progress on a neurotypical track for the first few years of their lives. But around the age of 4, Nance says, the lack of dystrophin begins to cause noticeable symptoms, causing gains in motor milestones to recede.

Prompting muscle cells to produce this missing protein would effectively cure the condition. Unfortunately, the gene that encodes dystrophin is large, making it difficult to fit inside current gene therapy vectors. However, says Nance, the new trial uses a workaround that partially fixes this problem: The dystrophin gene is trimmed down into “micro-dystrophin,” leaving only the essential pieces.

In June 2020, researchers at Nationwide Children’s Hospital in Columbus, Ohio, reported promising results from a phase 1/2 trial of this same gene therapy in a group of four young DMD patients, none of whom had yet started on corticosteroid therapy. After administering a single intravenous dose, this open-label trial followed participants for a year to assess safety, micro-dystrophin expression in muscle biopsies and functional outcomes in motor skills.

Not only was this therapy well tolerated, says Nance, but biopsy results showed that participants were producing micro-dystrophin and had begun doing the unimaginable — regaining lost motor function.

She hopes to see the same, she says, when she and her colleagues begin the next phase of the trial at Johns Hopkins in early 2021. They plan to recruit up to five boys under the age of 8. Although this trial will be randomized at first, study subjects on the placebo will eventually receive gene therapy if results continue to show potential.

“DMD has always been a terrible diagnosis to deliver,” she says. “But these conversations are starting to change because of the hope that new therapies may provide. This trial moving forward could be a big step toward getting meaningful treatment for these kids.”

Developing Implantable and Wearable Technology to Treat Spinal Cord Injury

Johns Hopkins neurosurgeons and biomedical engineers work to create wearable and implantable devices enabling continuous, postoperative treatment of acute, subacute and chronic spinal cord injury. The effort is funded by a $13.48 million grant from the Defense Advanced Research Projects Agency.

A medical illustration shows the back of the skull with an electrical implant placed where the neck and spine meet.

Individualized Care Through Translocation Testing

Johns Hopkins is among the few centers in the U.S. that identify tumors’ unique features using on-site fusion tests.

A conceptual image illustrates a DNA change in amber on a chromosome, an opaque blue X, on a black background.

Innovations in Care for Patients with Pediatric Epilepsy

For difficult epilepsy cases, Johns Hopkins experts use the latest, less invasive diagnostic and treatment tools.

A patient with electrodes attached to his head plays music on a drum pad as a doctor a child life specialist watch, smiling.