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Gene therapies for Mucopolysaccharidoses.

Alessandro RossiNicola Brunetti-Pierri
Published in: Journal of inherited metabolic disease (2023)
Current specific treatments for mucopolysaccharidoses (MPSs) include enzyme replacement therapy (ERT) and hematopoietic stem cell transplantation (HSCT). Both treatments are hampered by several limitations, including lack of efficacy on brain and skeletal manifestations, need for lifelong injections, and high costs. Therefore, more effective treatments are needed. Gene therapy in MPSs is aimed at obtaining high levels of the therapeutic enzyme in multiple tissues either by engrafted gene-modified hematopoietic stem progenitor cells (ex vivo) or by direct infusion of a viral vector expressing the therapeutic gene (in vivo). This review focuses on the most recent clinical progress in gene therapies for MPSs. The various gene therapy approaches with their strengths and limitations are discussed. This article is protected by copyright. All rights reserved.
Keyphrases
  • gene therapy
  • copy number
  • replacement therapy
  • genome wide
  • genome wide identification
  • acute myeloid leukemia
  • smoking cessation
  • resting state
  • functional connectivity
  • multiple sclerosis
  • genome wide analysis