Gene transfer in tissue repair: status, challenges and future directions

被引:27
作者
Eming, SA
Krieg, T
Davidson, JM
机构
[1] Univ Cologne, Dept Dermatol, D-50931 Cologne, Germany
[2] Vanderbilt Univ, Sch Med, Dept Pathol, Nashville, TN 37212 USA
[3] VA Med Ctr, Nashville, TN USA
关键词
gene transfer; growth factors; wound healing;
D O I
10.1517/14712598.4.9.1373
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Wound repair involves a complex interaction of various cell types, extracellular matrix molecules and soluble mediators. Details on signals controlling wound cell activities are beginning to emerge. In recent years this knowledge has been applied to a number of therapeutic strategies in soft tissue repair. Key challenges include re-adjusting the adult repair process in order to augment diseased healing processes, and providing the basis for a regenerative rather than a reparative wound environment. In particular, the local delivery of pluripotent growth factor molecules to the injured tissue has been intensively investigated over the past decade. Limited success of clinical trials indicates that an important aspect of the growth factor wound-healing paradigm is the effective delivery of these polypeptides to the wound site. A molecular genetic approach in which genetically modified cells synthesise and deliver the desired growth factor in a time-regulated manner is a powerful means to overcome the limitations associated with the (topical) application of recombinant growth factor proteins. This article summarises repair mechanisms and their failure, and gives an overview of techniques and studies applied to gene transfer in tissue repair. It also provides perspectives on potential targets for gene transfer technology.
引用
收藏
页码:1373 / 1386
页数:14
相关论文
共 129 条
[51]   Acceleration of cartilage repair by genetically modified chondrocytes over expressing bone morphogenetic protein-7 [J].
Hidaka, C ;
Goodrich, LR ;
Chen, CT ;
Warren, RF ;
Crystal, RG ;
Nixon, AJ .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2003, 21 (04) :573-583
[52]   Gene intervention in ligament and tendon: current status, challenges, future directions [J].
Hildebrand, KA ;
Frank, CB ;
Hart, DA .
GENE THERAPY, 2004, 11 (04) :368-378
[53]   Wound fluid from venous leg ulcers degrades plasminogen and reduces plasmin generation by keratinocytes [J].
Hoffman, R ;
Starkey, S ;
Coad, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1998, 111 (06) :1140-1144
[54]   Transcriptional targeting of adenoviral gene delivery info migrating wound keratinocytes using FiRE, a growth factor-inducible regulatory element [J].
Jaakkola, P ;
Ahonen, M ;
Kähäri, VM ;
Jalkanen, M .
GENE THERAPY, 2000, 7 (19) :1640-1647
[55]   Therapeutic success and efficacy of nonviral liposomal cDNA gene transfer to the skin in vivo is dose dependent [J].
Jeschke, MG ;
Richter, G ;
Herndon, DN ;
Geissler, EK ;
Hartl, M ;
Hofstätter, F ;
Jauch, KW ;
Perez-Polo, JR .
GENE THERAPY, 2001, 8 (23) :1777-1784
[56]   Cellular immune response to adenoviral vector infected cells does not require de novo viral gene expression:: Implications for gene therapy [J].
Kafri, T ;
Morgan, D ;
Krahl, T ;
Sarvetnick, N ;
Sherman, L ;
Verma, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (19) :11377-11382
[57]   Therapeutic gene delivery to the skin [J].
Khavari, PA .
MOLECULAR MEDICINE TODAY, 1997, 3 (12) :533-538
[58]  
KHAVARI PA, 1997, ADV CLIN RES, V5, P27
[59]   HIGH-VELOCITY MICROPROJECTILES FOR DELIVERING NUCLEIC-ACIDS INTO LIVING CELLS [J].
KLEIN, TM ;
WOLF, ED ;
WU, R ;
SANFORD, JC .
NATURE, 1987, 327 (6117) :70-73
[60]   Gene therapy with viral vectors [J].
Kootstra, NA ;
Verma, IM .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2003, 43 :413-439