Immune responses, not promoter inactivation, are responsible for decreased long-term expression following plasmid gene transfer into skeletal muscle

被引:47
作者
Wells, KE
Maule, J
Kingston, R
Foster, K
McMahon, J
Damien, E
Poole, A
Wells, DJ
机构
[1] CHARING CROSS & WESTMINSTER MED SCH,DEPT PHARMACOL,GENE TARGETING UNIT,LONDON W6 8RF,ENGLAND
[2] CHARING CROSS & WESTMINSTER MED SCH,DEPT CLIN NEUROSCI,LONDON W6 8RF,ENGLAND
[3] UNIV LONDON ROYAL VET COLL,DEPT VET BASIC SCI,LONDON NW1 0TU,ENGLAND
基金
英国医学研究理事会;
关键词
gene therapy; plasmid DNA; skeletal muscle; cytotoxic T-cells; immunology;
D O I
10.1016/S0014-5793(97)00329-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Long-term high-level in vivo gene expression appears to depend on the promoter chosen to drive the gene of choice, In many cases the promoter appears to 'switch off' some time after in vivo gene transfer, We demonstrate that, following intramuscular injection of beta-galactosidase reporter plasmids, promoter 'switch off is due to elimination of fibres expressing the transferred reporter gene by activation of a Th1 (cytotoxic) immune response, This finding, in the absence of stimulation of the immune system by viral vector proteins, has implications not only for gene transfer experiments but for the future of muscle-directed gene therapy. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:164 / 168
页数:5
相关论文
共 26 条
[1]   REMOVAL OF ENDOTOXIN FROM PROTEIN SOLUTIONS BY PHASE-SEPARATION USING TRITON X-114 [J].
AIDA, Y ;
PABST, MJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 1990, 132 (02) :191-195
[2]   INDUCTION OF CHRONIC RELAPSING EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS IN BIOZZI MICE [J].
BAKER, D ;
ONEILL, JK ;
GSCHMEISSNER, SE ;
WILCOX, CE ;
BUTTER, C ;
TURK, JL .
JOURNAL OF NEUROIMMUNOLOGY, 1990, 28 (03) :261-270
[3]   A VERY STRONG ENHANCER IS LOCATED UPSTREAM OF AN IMMEDIATE EARLY GENE OF HUMAN CYTOMEGALO-VIRUS [J].
BOSHART, M ;
WEBER, F ;
JAHN, G ;
DORSCHHASLER, K ;
FLECKENSTEIN, B ;
SCHAFFNER, W .
CELL, 1985, 41 (02) :521-530
[4]   CELLULAR AND HUMORAL IMMUNE-RESPONSES TO ADENOVIRAL VECTORS CONTAINING FACTOR-IX GENE - TOLERIZATION OF FACTOR-IX AND VECTOR ANTIGENS ALLOWS FOR LONG-TERM EXPRESSION [J].
DAI, YF ;
SCHWARZ, EM ;
GU, DL ;
ZHANG, WW ;
SARVETNICK, N ;
VERMA, IM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (05) :1401-1405
[5]  
DANKO I, 1994, GENE THER, V1, P114
[6]   PLASMID DNA IS SUPERIOR TO VIRAL VECTORS FOR DIRECT GENE-TRANSFER INTO ADULT-MOUSE SKELETAL-MUSCLE [J].
DAVIS, HL ;
DEMENEIX, BA ;
QUANTIN, B ;
COULOMBE, J ;
WHALEN, RG .
HUMAN GENE THERAPY, 1993, 4 (06) :733-740
[7]   Systematic analysis of repeated gene delivery into animal lungs with a recombinant adenovirus vector [J].
Dong, JY ;
Wang, DH ;
VanGinkel, FW ;
Pascual, DW ;
Frizzell, RA .
HUMAN GENE THERAPY, 1996, 7 (03) :319-331
[8]   EFFICIENCY OF IN-VIVO GENE-TRANSFER USING MURINE RETROVIRAL VECTORS IS STRAIN-DEPENDENT IN MICE [J].
FASSATI, A ;
WELLS, DJ ;
WALSH, FS ;
DICKSON, G .
HUMAN GENE THERAPY, 1995, 6 (09) :1177-1183
[9]  
Flecknell P., 1987, LAB ANIMAL ANAESTHES
[10]  
GAVIN MA, 1993, J IMMUNOL, V151, P3971