Gene therapy applications for fracture-healing

被引:46
作者
Carofino, Bradley C.
Lieberman, Jay R.
机构
关键词
D O I
10.2106/JBJS.G.01546
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Biologic therapies to promote fracture-healing such as use of bone morphogenetic proteins (BMPs) are being increasingly employed in multiple clinical scenarios. However, it has been challenging to design therapies that deliver sufficient quantities of protein over a sustained time period. A potential solution is the application of gene therapy that transfers genetic information to host cells at the fracture site, resulting in the continuous and localized production of the desired proteins. This approach has demonstrated tremendous potential in preclinical animal models of fracture-healing. This article will review the current state of gene therapy approaches to fracture-healing with an emphasis on potential clinical applications.
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页码:99 / 110
页数:12
相关论文
共 100 条
[61]   Immune response to recombinant adenovirus in humans: Capsid components from viral input are targets for vector-specific cytotoxic T lymphocytes [J].
Molinier-Frenkel, V ;
Gawery-Segard, H ;
Mentali, M ;
Le Boulaire, C ;
Ribault, S ;
Boulanger, P ;
Tursz, T ;
Guillet, JG ;
Farace, F .
JOURNAL OF VIROLOGY, 2000, 74 (16) :7678-7682
[62]   Exogenously regulated stem cell-mediated gene therapy for bone regeneration [J].
Moutsatsos, IK ;
Turgeman, G ;
Zhou, SH ;
Kurkalli, BG ;
Pelled, G ;
Tzur, L ;
Kelley, P ;
Stumm, N ;
Mi, S ;
Müller, R ;
Zilberman, Y ;
Gazit, D .
MOLECULAR THERAPY, 2001, 3 (04) :449-461
[63]  
Musgrave Douglas S, 2002, J Am Acad Orthop Surg, V10, P6
[64]   Human skeletal muscle cells in ex vivo gene therapy to deliver bone morphogenetic protein-2 [J].
Musgrave, DS ;
Pruchnic, R ;
Bosch, P ;
Ziran, BH ;
Whalen, J ;
Huard, J .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2002, 84B :120-127
[65]   Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector [J].
Naldini, L ;
Blomer, U ;
Gage, FH ;
Trono, D ;
Verma, IM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (21) :11382-11388
[66]   In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector [J].
Naldini, L ;
Blomer, U ;
Gallay, P ;
Ory, D ;
Mulligan, R ;
Gage, FH ;
Verma, IM ;
Trono, D .
SCIENCE, 1996, 272 (5259) :263-267
[67]   Combination of porous hydroxyapatite and cationic liposomes as a vector for BMP-2 gene therapy [J].
Ono, I ;
Yamashita, T ;
Jin, HY ;
Ito, Y ;
Hamada, H ;
Akasaka, Y ;
Nakasu, M ;
Ogawa, T ;
Jimbow, K .
BIOMATERIALS, 2004, 25 (19) :4709-4718
[68]   VEGF improves, whereas sFlt1 inhibits, BMP2-induced bone formation and bone healing through modulation of angiogenesis [J].
Peng, HR ;
Usas, A ;
Olshanski, A ;
Ho, AM ;
Gearhart, B ;
Cooper, GM ;
Huard, J .
JOURNAL OF BONE AND MINERAL RESEARCH, 2005, 20 (11) :2017-2027
[69]   Noggin improves bone healing elicited by muscle stem cells expressing inducible BMP4 [J].
Peng, HR ;
Usas, A ;
Hannallah, D ;
Olshanski, A ;
Cooper, GM ;
Huard, J .
MOLECULAR THERAPY, 2005, 12 (02) :239-246
[70]  
Peng HR, 2004, MOL THER, V9, P885, DOI 10.1016/j.ymthe.2004.02.023