Pharmacologic transgene control systems for gene therapy

被引:66
作者
Weber, Wilfried [1 ]
Fussenegger, Martin [1 ]
机构
[1] ETH, Inst Chem & Bioengn, Swiss Fed Inst Technol, CH-8093 Zurich, Switzerland
关键词
geneswitch; inducible expression; vival vector; gene regulation;
D O I
10.1002/jgm.903
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
Pharmacologic transgene-expression dosing is considered essential for future gene therapy scenarios. Genetic interventions require precise transcription or translation fine-tuning of therapeutic transgenes to enable their titration into the therapeutic window, to adapt them to daily changing dosing regimes of the patient, to integrate them seamlessly into the patient's transcriptome orchestra, and to terminate their expression after successful therapy. In recent years, decisive progress has been achieved in designing high-precision trigger-inducible mammalian transgene control modalities responsive to clinically licensed and inert heterologous molecules or to endogenous physiologic signals. Availability of a portfolio of compatible transcription control systems has enabled assembly of higher-order control circuitries providing simultaneous or independent control of several transgenes and the design of (semi-) synthetic gene networks, which emulate digital expression switches, regulatory transcription cascades, epigenetic expression imprinting, and cellular transcription memories. This review provides an overview of cutting-edge developments in transgene control systems, of the design of synthetic gene networks, and of the delivery of such systems for the prototype treatment of prominent human disease phenotypes. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:535 / 556
页数:22
相关论文
共 206 条
[1]   Ligand-dependent regulation of vascular endothelial growth factor and erythropoietin expression by a plasmid-based autoinducible GeneSwitch system [J].
Abruzzese, RV ;
Godin, D ;
Mehta, V ;
Perrard, JL ;
French, M ;
Nelson, W ;
Howell, G ;
Coleman, M ;
O'Malley, BW ;
Nordstrom, JL .
MOLECULAR THERAPY, 2000, 2 (03) :276-287
[2]   Second-generation tetracycline-regulatable promoter: repositioned tet operator elements optimize transactivator synergy while shorter minimal promoter offers tight basal leakiness [J].
Agha-Mohammadi, S ;
O'Malley, M ;
Etemad, A ;
Wang, Z ;
Xiao, X ;
Lotze, MT .
JOURNAL OF GENE MEDICINE, 2004, 6 (07) :817-828
[3]   A novel tetracycline-dependent transactivator with E2F4 transcriptional activation domain [J].
Akagi, Kiwamu ;
Kanai, Masayuki ;
Saya, Hideyuki ;
Kozu, Tomoko ;
Berns, Anton .
NUCLEIC ACIDS RESEARCH, 2001, 29 (04) :23
[4]   DNA electrotransfer:: its principles and an updated review of its therapeutic applications [J].
André, F ;
Mir, LM .
GENE THERAPY, 2004, 11 (Suppl 1) :S33-S42
[5]   Tetracycline-inducible interleukin-10 gene transfer mediated by an adeno-associated virus:: Application to experimental arthritis [J].
Apparailly, F ;
Millet, V ;
Noël, D ;
Jacquet, C ;
Sany, J ;
Jorgensen, C .
HUMAN GENE THERAPY, 2002, 13 (10) :1179-1188
[6]   Design of a novel mammalian screening system for the detection of bioavailable, non-cytotoxic streptogramin antibiotics [J].
Aubel, D ;
Morris, R ;
Lennon, B ;
Rimann, M ;
Kaufmann, H ;
Folcher, M ;
Bailey, JE ;
Thompson, CJ ;
Fussenegger, M .
JOURNAL OF ANTIBIOTICS, 2001, 54 (01) :44-55
[7]   Constitutive and regulated expression of processed insulin following in vivo hepatic gene transfer [J].
Auricchio, A ;
Gao, GP ;
Yu, QC ;
Raper, S ;
Rivera, VM ;
Clackson, T ;
Wilson, JM .
GENE THERAPY, 2002, 9 (14) :963-971
[8]   Pharmacological regulation of protein expression from adeno-associated viral vectors in the eye [J].
Auricchio, A ;
Rivera, VM ;
Clackson, T ;
O'Connor, EE ;
Maguire, AM ;
Tolentino, MJ ;
Bennett, J ;
Wilson, JM .
MOLECULAR THERAPY, 2002, 6 (02) :238-242
[9]   Regulated and liver-specific tamarin alpha interferon gene delivery by a helper-dependent adenoviral vector [J].
Aurisicchio, L ;
De Tomassi, A ;
La Monica, N ;
Ciliberto, G ;
Traboni, C ;
Palombo, F .
JOURNAL OF VIROLOGY, 2005, 79 (11) :6772-6780
[10]   Combinations of the alpha-helix-turn-alpha-helix motif of TetR with respective residues from LacI or 434Cro: DNA recognition, inducer binding, and urea-dependent denaturation [J].
Backes, H ;
Berens, C ;
Helbl, V ;
Walter, S ;
Schmid, FX ;
Hillen, W .
BIOCHEMISTRY, 1997, 36 (18) :5311-5322