Cited by 151Bone Tissue Engineering MaterialsVirus-based gene therapy researchBone Metabolism and Diseases

Bone tissue engineering by gene delivery

KOFRON, M, LAURENCIN, C·2006·Advanced Drug Delivery Reviews

Abstract

Recombinant human bone morphogenetic protein-2 and -7 were recently granted United States Food and Drug Administration approval for select clinical applications in bone repair. While significant progress has been made in the delivery of recombinant osteogenic factor to promote bone healing, the short half-life and instability of the protein requires the delivery of milligram quantities of factor or multiple dosages. The potential of gene therapy for bone regeneration is the delivery of physiological levels of therapeutic protein using natural cellular mechanisms. Experimental investigations have demonstrated this approach uses lower dosages of factor to yield bone healing equivalent to that achieved via the administration of recombinant factor or use of bone grafts. The current states of gene delivery for bone tissue engineering applications and challenges to be met are presented in this review. Over the past couple of years, studies have continued to examine the delivery of the osteogenic factor bone morphogenetic protein using gene therapies. The importance of angiogenesis to bone formation has prompted the development of vascular endothelial growth factor gene expression systems for bone regeneration. Viral vectors, in combination with allograft bone, have been investigated to improve existing surgical care. Newly constructed vectors with reduced immunogenicity and regulated gene expression systems provide a greater degree of control over the timing and level of gene expre…

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Crossref · 10.1016/j.addr.2006.03.008

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  • Autologous and allogeneic bone grafts are the most frequently employed clinical techniques for bone repair but have limitations including donor-site defects, immune rejection, and surgical pain.

    “Autologous and allogeneic bone grafts are the most frequently employed clinical techniques [129,130]. However, there are still some limitations to these treatments, such as the risk of creating new defects at the donor site, potential immune rejection, and the pain associated with surgical procedures [131,132].”

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Authors
KOFRON, M., & LAURENCIN, C.
Affiliations
University of Virginia (US)
Corresponding author
LAURENCIN, C
Venue
Advanced Drug Delivery Reviews
Publisher
Elsevier BV
Published
2006-07-07
Volume
58
Issue
4
Pages
555-576
ISSN
0169-409X (ISSN-L)
OpenAlex
W2158773351
Cited by
151
References
1
Citations by year
2025: 2 · 2024: 7 · 2023: 7 · 2022: 6 · 2021: 6 · 2020: 4 · 2019: 7 · 2018: 2 · 2017: 6 · 2016: 9 · 2015: 9 · 2014: 11 · 2013: 7 · 2012: 13
FWCI
7.92
Type
journal article
Language
en
Open access
closed
Locations
  • Advanced Drug Delivery Reviews (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
Keywords
bone tissue engineering, gene delivery, gene therapy, BMP-2, bone morphogenetic protein-7, bone regeneration, angiogenesis, vascular endothelial growth factor, viral vectors, bone allografts, regulated gene expression, osteogenesis imperfecta, hereditary bone disease, bone defects, fracture
MeSH terms
Animals, Bone Diseases, Bone Regeneration, Genetic Vectors, Growth Substances, Humans, Genetic Therapy, Gene Transfer Techniques, Tissue Engineering, Stem Cell Transplantation

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