Gene therapy approaches to regenerating the musculoskeletal system

被引:171
作者
Evans, Christopher H. [1 ]
Huard, Johnny [2 ]
机构
[1] Mayo Clin, Rehabil Med Res Ctr, 200 First St SW, Rochester, MN 55905 USA
[2] Univ Pittsburgh, Stem Cell Res Ctr, Dept Orthopaed Surg, Pittsburgh, PA 15219 USA
关键词
MESENCHYMAL STEM-CELLS; BONE MORPHOGENETIC PROTEIN-2; ARTICULAR-CARTILAGE DEFECTS; GROWTH-FACTOR-I; RAAV-MEDIATED OVEREXPRESSION; SKELETAL-MUSCLE; RAT MODEL; TRANSFORMING GROWTH-FACTOR-BETA-1; HETEROTOPIC OSSIFICATION; INTERVERTEBRAL DISC;
D O I
10.1038/nrrheum.2015.28
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Injuries to the musculoskeletal system are common, debilitating and expensive. In many cases, healing is imperfect, which leads to chronic impairment. Gene transfer might improve repair and regeneration at sites of injury by enabling the local, sustained and potentially regulated expression of therapeutic gene products; such products include morphogens, growth factors and anti-inflammatory agents. Proteins produced endogenously as a result of gene transfer are nascent molecules that have undergone post-translational modification. In addition, gene transfer offers particular advantages for the delivery of products with an intracellular site of action, such as transcription factors and noncoding RNAs, and proteins that need to be inserted into a cell compartment, such as a membrane. Transgenes can be delivered by viral or nonviral vectors via in vivo or ex vivo protocols using progenitor or differentiated cells. The first gene transfer clinical trials for osteoarthritis and cartilage repair have already been completed. Various bone-healing protocols are at an advanced stage of development, including studies with large animals that could lead to human trials. Other applications in the repair and regeneration of skeletal muscle, intervertebral disc, meniscus, ligament and tendon are in preclinical development. In addition to scientific, medical and safety considerations, clinical translation is constrained by social, financial and logistical issues.
引用
收藏
页码:234 / 242
页数:9
相关论文
共 129 条
[1]   Suicide gene approach using a dual-expression lentiviral vector to enhance the safety of ex vivo gene therapy for bone repair [J].
Alaee, F. ;
Sugiyama, O. ;
Virk, M. S. ;
Tang, H. ;
Drissi, H. ;
Lichtler, A. C. ;
Lieberman, J. R. .
GENE THERAPY, 2014, 21 (02) :139-147
[2]   Conversion of Human Bone Marrow-Derived Mesenchymal Stem Cells into Tendon Progenitor Cells by Ectopic Expression of Scleraxis [J].
Alberton, Paolo ;
Popov, Cvetan ;
Praegert, Markus ;
Kohler, Julia ;
Shukunami, Chisa ;
Schieker, Matthias ;
Docheva, Denitsa .
STEM CELLS AND DEVELOPMENT, 2012, 21 (06) :846-858
[3]  
Baltzer AWA, 2000, CLIN ORTHOP RELAT R, pS120
[4]   A gene therapy approach to accelerating bone healing - Evaluation of gene expression in a New Zealand white rabbit model [J].
Baltzer, AWA ;
Lattermann, C ;
Whalen, JD ;
Braunstein, S ;
Robbins, PD ;
Evans, CH .
KNEE SURGERY SPORTS TRAUMATOLOGY ARTHROSCOPY, 1999, 7 (03) :197-202
[5]   Freeze-dried tendon Allografts as tissue-engineering scaffolds for gdf5 gene delivery [J].
Basile, Patrick ;
Dadali, Tulin ;
Jacobson, Justin ;
Hasslund, Sys ;
Ulrich-Vinther, Michael ;
Soballe, Kjeld ;
Nishio, Yasuhiko ;
Drissi, M. Hicham ;
Langstein, Howard N. ;
Mitten, David J. ;
O'Keefe, Regis J. ;
Schwarz, Edward M. ;
Awad, Hani A. .
MOLECULAR THERAPY, 2008, 16 (03) :466-473
[6]   Angiotensin II receptor blockade administered after injury improves muscle regeneration and decreases fibrosis in normal skeletal muscle [J].
Bedair, Hany S. ;
Karthikeyan, Tharun ;
Quintero, Andres ;
Li, Yong ;
Huard, Johnny .
AMERICAN JOURNAL OF SPORTS MEDICINE, 2008, 36 (08) :1548-1554
[7]   Adenoviral-mediated transfer of human BMP-6 gene accelerates healing in a rabbit ulnar osteotomy model [J].
Bertone, AL ;
Pittman, DD ;
Bouxsein, ML ;
Li, J ;
Clancy, B ;
Seeherman, HJ .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2004, 22 (06) :1261-1270
[8]   Delayed administration of adenoviral BMP-2 vector improves the formation of bone in osseous defects [J].
Betz, O. B. ;
Betz, V. M. ;
Nazarian, A. ;
Egermann, M. ;
Gerstenfeld, L. C. ;
Einhorn, T. A. ;
Vrahas, M. S. ;
Bouxsein, M. L. ;
Evans, C. H. .
GENE THERAPY, 2007, 14 (13) :1039-1044
[9]   Direct percutaneous gene delivery to enhance healing of segmental bone defects [J].
Betz, OB ;
Betz, VM ;
Nazarian, A ;
Pilapil, CG ;
Vrahas, MS ;
Bouxsein, ML ;
Gerstenfeld, LC ;
Einhorn, TA ;
Evans, CH .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2006, 88A (02) :355-365
[10]   Healing of segmental bone defects by direct percutaneous gene delivery: Effect of vector dose [J].
Betz, Volker M. ;
Betz, Oliver B. ;
Glatt, Vaida ;
Gerstenfeld, Louis C. ;
Einhorn, Thomas A. ;
Bouxsein, Mary L. ;
Vrahas, Mark S. ;
Evans, Christopher H. .
HUMAN GENE THERAPY, 2007, 18 (10) :907-915