JOURNAL ARTICLE
REVIEW

Pompe disease gene therapy

Barry J Byrne, Darin J Falk, Christina A Pacak, Sushrusha Nayak, Roland W Herzog, Melissa E Elder, Shelley W Collins, Thomas J Conlon, Nathalie Clement, Brian D Cleaver, Denise A Cloutier, Stacy L Porvasnik, Saleem Islam, Mai K Elmallah, Anatole Martin, Barbara K Smith, David D Fuller, Lee Ann Lawson, Cathryn S Mah
Human Molecular Genetics 2011 April 15, 20 (R1): R61-8
21518733
Pompe disease is an autosomal recessive metabolic myopathy caused by the deficiency of the lysosomal enzyme acid alpha-glucosidase and results in cellular lysosomal and cytoplasmic glycogen accumulation. A wide spectrum of disease exists from hypotonia and severe cardiac hypertrophy in the first few months of life due to severe mutations to a milder form with the onset of symptoms in adulthood. In either condition, the involvement of several systems leads to progressive weakness and disability. In early-onset severe cases, the natural history is characteristically cardiorespiratory failure and death in the first year of life. Since the advent of enzyme replacement therapy (ERT), the clinical outcomes have improved. However, it has become apparent that a new natural history is being defined in which some patients have substantial improvement following ERT, while others develop chronic disability reminiscent of the late-onset disease. In order to improve on the current clinical outcomes in Pompe patients with diminished clinical response to ERT, we sought to address the cause and potential for the treatment of disease manifestations which are not amenable to ERT. In this review, we will focus on the preclinical studies that are relevant to the development of a gene therapy strategy for Pompe disease, and have led to the first clinical trial of recombinant adeno-associated virus-mediated gene-based therapy for Pompe disease. We will cover the preliminary laboratory studies and rationale for a clinical trial, which is based on the treatment of the high rate of respiratory failure in the early-onset patients receiving ERT.

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