The use of bone morphogenetic protein gene therapy in craniofacial bone repair

被引:67
作者
Alden, TD
Beres, EJ
Laurent, JS
Engh, JA
Das, S
London, SD
Jane, JA
Hudson, SB
Helm, GA
机构
[1] Univ Virginia, Dept Neurosurg, Hlth Sci Ctr, Charlottesville, VA 22908 USA
[2] Univ Virginia, Dept Biomed Engn, Charlottesville, VA 22908 USA
[3] Univ Virginia, Dept Otolaryngol Head & Neck Surg, Charlottesville, VA 22908 USA
关键词
BMP-2; BMP-9; gene therapy; osteogenesis; adenovirus;
D O I
10.1097/00001665-200011010-00005
中图分类号
R61 [外科手术学];
学科分类号
摘要
Bone morphogenetic proteins (BMPs) are capable of inducing endochondral bone formation when applied on biologic carriers in numerous mammalian in vivo assay systems. Bone morphogenetic protein gene therapy is also currently being developed to promote osteogenesis for clinical indications such as spinal fusions, craniofacial bone loss, and osteoporosis. In this study, critical-sized mandibular defects were treated with a control adenoviral vector (Ad-P-gal), a BMP-2 adenoviral vector (Ad-BMP-2), or a BMP-9 adenoviral vector (Ad-BMP-9). Gross tissue examination, radiographic analysis, and histologic analysis demonstrated significant bony healing in the BMP treated groups compared to controls. Osteogenesis was limited to the bony defect, without extension into the surrounding soft tissues. The study suggests that with further development, BMP gene therapy may be potentially useful for repair of bony defects in the craniofacial region.
引用
收藏
页码:24 / 30
页数:7
相关论文
共 61 条
[51]   REPAIR OF CRITICAL SIZE RAT CALVARIAL DEFECTS USING EXTRACELLULAR-MATRIX PROTEIN GELS [J].
SWEENEY, TM ;
OPPERMAN, LA ;
PERSING, JA ;
OGLE, RC .
JOURNAL OF NEUROSURGERY, 1995, 83 (04) :710-715
[52]  
TAGAKI K, 1982, CLIN ORTHOP RELAT R, V171, P224
[53]  
TIMMONS MJ, 1986, BRIT J PLAST SURG, V39, P176, DOI 10.1016/0007-1226(86)90078-0
[54]   Oromandibular reconstruction using microvascular composite flaps - Report of 210 cases [J].
Urken, ML ;
Buchbinder, D ;
Costantino, PD ;
Sinha, U ;
Okay, D ;
Lawson, W ;
Biller, HF .
ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 1998, 124 (01) :46-55
[55]  
Wurzler KK, 1998, J CRANIOFAC SURG, V9, P131
[56]   Role of viral antigens in destructive cellular immune responses to adenovirus vector-transduced cells in mouse lungs [J].
Yang, YP ;
Su, Q ;
Wilson, JM .
JOURNAL OF VIROLOGY, 1996, 70 (10) :7209-7212
[57]   THE HEALING OF SEGMENTAL BONE DEFECTS, INDUCED BY RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN (RHBMP-2) - A RADIOGRAPHIC, HISTOLOGICAL, AND BIOMECHANICAL STUDY IN RATS [J].
YASKO, AW ;
LANE, JM ;
FELLINGER, EJ ;
ROSEN, V ;
WOZNEY, JM ;
WANG, EA .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1992, 74A (05) :659-670
[58]   IN-VIVO EVALUATION OF THE SAFETY OF ADENOVIRUS-MEDIATED TRANSFER OF THE HUMAN CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR CDNA TO THE LUNG [J].
YEI, SP ;
MITTEREDER, N ;
WERT, S ;
WHITSETT, JA ;
WILMOTT, RW ;
TRAPNELL, BC .
HUMAN GENE THERAPY, 1994, 5 (06) :731-744
[59]  
Zellin G, 1997, J BIOMED MATER RES, V35, P181
[60]   Opposite effects of recombinant human transforming growth factor-β1 on bone regeneration in vivo:: Effects of exclusion of periosteal cells by microporous membrane [J].
Zellin, G ;
Beck, S ;
Hardwick, R ;
Linde, A .
BONE, 1998, 22 (06) :613-620