Assessment of different virus-mediated approaches for retinal gene therapy of Usher 1B

Adv Exp Med Biol. 2014:801:725-31. doi: 10.1007/978-1-4614-3209-8_91.

Abstract

Usher syndrome type 1B, which is characterized by congenital deafness and progressive retinal degeneration, is caused by the loss of the function of MYO7A. Prevention of the retinal degeneration should be possible by delivering functional MYO7A to retinal cells. Although this approach has been used successfully in clinical trials for Leber congenital amaurosis (LCA2), it remains a challenge for Usher 1B because of the large size of the MYO7A cDNA. Different viral vectors have been tested for use in MYO7A gene therapy. Here, we review approaches with lentiviruses, which can accommodate larger genes, as well as attempts to use adeno-associated virus (AAV), which has a smaller packaging capacity. In conclusion, both types of viral vector appear to be effective. Despite concerns about the ability of lentiviruses to access the photoreceptor cells, a phenotype of the photoreceptors of Myo7a-mutant mice can be corrected. And although MYO7A cDNA is significantly larger than the nominal carrying capacity of AAV, AAV-MYO7A in single vectors also corrected Myo7a-mutant phenotypes in photoreceptor and RPE cells. Interestingly, however, a dual AAV vector approach was found to be much less effective.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Dependovirus / genetics*
  • Genetic Therapy / methods*
  • Genetic Vectors
  • Humans
  • Lentivirus / genetics*
  • Mice
  • Mice, Knockout
  • Myosin VIIa
  • Myosins / genetics*
  • Usher Syndromes / genetics
  • Usher Syndromes / therapy*

Substances

  • MYO7A protein, human
  • Myo7a protein, mouse
  • Myosin VIIa
  • Myosins

Supplementary concepts

  • Usher syndrome, type 1B