Gene therapy for tissue repair: approaches and prospects

被引:26
作者
Eming, SA
Morgan, JR
Berger, A
机构
[1] HARVARD UNIV,SCH MED,MASSACHUSETTS GEN HOSP,SHRINERS BURNS INST,SURG SERV,CAMBRIDGE,MA 02137
[2] KRANKENHAUS OSTSTADT,DEPT PLAST SURG,D-30659 HANNOVER,GERMANY
[3] UNIV HANNOVER,DEPT PLAST SURG,HANNOVER,GERMANY
来源
BRITISH JOURNAL OF PLASTIC SURGERY | 1997年 / 50卷 / 07期
关键词
D O I
10.1016/S0007-1226(97)91297-2
中图分类号
R61 [外科手术学];
学科分类号
摘要
Recent advances in molecular biology have resulted in the development of new technologies for the introduction and expression of genes in human somatic cells. This emerging field, known as gene therapy, is broadly defined as the transfer of genetic material to cells/tissues in order to achieve a therapeutic effect for inherited as well as acquired diseases. We and others are exploring the potential application of this technology to tissue repair. One primary focus has been to transfer genes encoding wound healing growth factors, a broad class of proteins which control local events in tissues such as cell proliferation, cell migration and the formation of extracellular matrix. Using several different strategies for gene transfer, wound healing growth factor genes have been introduced and expressed in cells and tissues in vitro as well as in vivo. Various experimental models of wound healing and tissue repair have been used to evaluate the efficacy of this new and exciting approach to tissue repair.
引用
收藏
页码:491 / 500
页数:10
相关论文
共 91 条
[1]  
Amadio P. C., 1992, WOUND HEALING BIOCH, P384
[2]   GENE-EXPRESSION IN IMPLANTED RAT HEPATOCYTES FOLLOWING RETROVIRAL-MEDIATED GENE-TRANSFER [J].
ANDERSON, KD ;
THOMPSON, JA ;
DIPIETRO, JM ;
MONTGOMERY, KT ;
REID, LM ;
ANDERSON, WF .
SOMATIC CELL AND MOLECULAR GENETICS, 1989, 15 (03) :215-227
[3]   IN-VIVO TRANSFER AND EXPRESSION OF A HUMAN EPIDERMAL GROWTH-FACTOR GENE ACCELERATES WOUND REPAIR [J].
ANDREE, C ;
SWAIN, WF ;
PAGE, CP ;
MACKLIN, MD ;
SLAMA, J ;
HATZIS, D ;
ERIKSSON, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (25) :12188-12192
[4]   INTRAARTICULAR EXPRESSION OF BIOLOGICALLY-ACTIVE INTERLEUKIN-1 RECEPTOR-ANTAGONIST PROTEIN BY EX-VIVO GENE-TRANSFER [J].
BANDARA, G ;
MUELLER, GM ;
GALEALAURI, J ;
TINDAL, MH ;
GEORGESCU, HI ;
SUCHANEK, MK ;
HUNG, GL ;
GLORIOSO, JC ;
ROBBINS, PD ;
EVANS, CH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (22) :10764-10768
[5]   TRANSPLANTATION OF TRANSDUCED CHONDROCYTES PROTECTS ARTICULAR-CARTILAGE FROM INTERLEUKIN 1-INDUCED EXTRACELLULAR-MATRIX DEGRADATION [J].
BARAGI, VM ;
RENKIEWICZ, RR ;
JORDAN, H ;
BONADIO, J ;
HARTMAN, JW ;
ROESSLER, BJ .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (05) :2454-2460
[6]   SYSTEMIC DELIVERY OF RECOMBINANT PROTEINS BY GENETICALLY MODIFIED MYOBLASTS [J].
BARR, E ;
LEIDEN, JM .
SCIENCE, 1991, 254 (5037) :1507-1509
[7]  
BENN SI, IN PRESS J CLIN INVE
[8]   Adenoviral-mediated herpes simplex virus-thymidine kinase gene transfer in vivo for treatment of experimental human melanoma [J].
Bonnekoh, B ;
Greenhalgh, DA ;
Bundman, DS ;
Kosai, K ;
Chen, SH ;
Finegold, MJ ;
Krieg, T ;
Woo, SLC ;
Roop, DR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 106 (06) :1163-1168
[9]   TREATMENT OF DEEP CARTILAGE DEFECTS IN THE KNEE WITH AUTOLOGOUS CHONDROCYTE TRANSPLANTATION [J].
BRITTBERG, M ;
LINDAHL, A ;
NILSSON, A ;
OHLSSON, C ;
ISAKSSON, O ;
PETERSON, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (14) :889-895
[10]   FUNCTIONAL RETROVIRAL VECTOR FOR GENE-THERAPY OF XERODERMA-PIGMENTOSUM GROUP-D PATIENTS [J].
CARREAU, M ;
QUILLIET, X ;
EVENO, E ;
SALVETTI, A ;
DANOS, O ;
HEARD, JM ;
MEZZINA, M ;
SARASIN, A .
HUMAN GENE THERAPY, 1995, 6 (10) :1307-1315