A Brief Review of Duchenne Muscular Dystrophy Treatment Options, with an Emphasis on Two Novel Strategies.
Ahlke HeydemannMaria SiemionowPublished in: Biomedicines (2023)
Despite the full cloning of the Dystrophin cDNA 35 years ago, no effective treatment exists for the Duchenne Muscular Dystrophy (DMD) patients who have a mutation in this gene. Many treatment options have been considered, investigated preclinically and some clinically, but none have circumvented all barriers and effectively treated the disease without burdening the patients with severe side-effects. However, currently, many novel therapies are in the pipelines of research labs and pharmaceutical companies and many of these have progressed to clinical trials. A brief review of these promising therapies is presented, followed by a description of two novel technologies that when utilized together effectively treat the disease in the mdx mouse model. One novel technology is to generate chimeric cells from the patient's own cells and a normal donor. The other technology is to systemically transplant these cells into the femur via the intraosseous route.
Keyphrases
- peritoneal dialysis
- duchenne muscular dystrophy
- end stage renal disease
- induced apoptosis
- clinical trial
- mouse model
- cell cycle arrest
- muscular dystrophy
- chronic kidney disease
- stem cells
- gene expression
- early onset
- newly diagnosed
- randomized controlled trial
- cell therapy
- ejection fraction
- copy number
- pi k akt
- prognostic factors
- mass spectrometry
- open label
- postmenopausal women
- combination therapy
- bone mineral density
- mesenchymal stem cells
- cell proliferation
- replacement therapy
- transcription factor
- patient reported
- atomic force microscopy