Orthopaedic gene therapy using recombinant adeno-associated virus vectors

Arch Oral Biol. 2011 Jul;56(7):619-28. doi: 10.1016/j.archoralbio.2010.12.010. Epub 2011 Feb 26.

Abstract

Use of recombinant adeno-associated virus (rAAV) vectors is increasingly gaining popularity in gene therapy because of their desirable properties, including lack of pathogenicity, efficient transduction of dividing and non-dividing cells, and sustained maintenance of the viral genome. It is these features of rAAV vectors that made them the focus for gene-based therapy of skeletal tissue regeneration. This review outlines the biological characteristics of adeno-associated virus (AAV), states the biological processing as well as current advances of rAAV vectors, and describes the recent achievements of their applications in orthopaedic and craniofacial surgery.

Publication types

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

MeSH terms

  • Bone Diseases / therapy*
  • Bone Regeneration / genetics
  • Dependovirus / genetics*
  • Genetic Therapy / methods*
  • Genetic Vectors / genetics
  • Genetic Vectors / therapeutic use*
  • Genome, Viral / genetics
  • Humans
  • Orthopedic Procedures
  • Plasmids / genetics
  • Plasmids / therapeutic use
  • Transduction, Genetic / methods