The induction of inflammation by adenovirus vectors used for gene therapy

被引:29
作者
Cotter, MJ [1 ]
Muruve, DA [1 ]
机构
[1] Univ Calgary, Calgary, AB T2N 4N1, Canada
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2005年 / 10卷
关键词
adenovirus vectors; gene therapy; treatment; gene; innate immunity; inflammation; chemokines; cytokines; signal transduction; review;
D O I
10.2741/1603
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
The ability to repair or enhance an individual's genetic make-up provides the sublime opportunity to ameliorate or eliminate many clinical disorders that affect mankind. Gene therapy is thus a revolutionary clinical strategy that may potentially treat an array of genetic and non-genetic diseases, as well as a novel method for drug delivery and vaccination. To these ends, adenovirus vectors are currently the most promising means to deliver specific genes of interest into target cells of the patient. A major limitation of the use of adenovirus vectors in clinical trials, however, is the rapidly induced inflammatory response against these infectious particles. This review aims to describe the cellular and molecular mechanisms involved in the adenovirus-mediated inflammatory response.
引用
收藏
页码:1098 / 1105
页数:8
相关论文
共 51 条
[21]   Adenovirus endocytosis via αv integrins requires phosphoinositide-3-OH kinase [J].
Li, EG ;
Stupack, D ;
Klemke, R ;
Cheresh, DA ;
Nemerow, GR .
JOURNAL OF VIROLOGY, 1998, 72 (03) :2055-2061
[22]  
Li Y, 2002, EUR J IMMUNOL, V32, P3443, DOI 10.1002/1521-4141(200212)32:12<3443::AID-IMMU3443>3.0.CO
[23]  
2-F
[24]   Recombinant adenoviruses with large deletions generated by cre-mediated excision exhibit different biological properties compared with first-generation vectors in vitro and in vivo [J].
Lieber, A ;
He, CY ;
Kirillova, I ;
Kay, MA .
JOURNAL OF VIROLOGY, 1996, 70 (12) :8944-8960
[25]   The role of Kupffer cell activation and viral gene expression in early liver toxicity after infusion of recombinant adenovirus vectors [J].
Lieber, A ;
He, CY ;
Meuse, L ;
Schowalter, D ;
Kirillova, I ;
Winther, B ;
Kay, MA .
JOURNAL OF VIROLOGY, 1997, 71 (11) :8798-8807
[26]   The role of capsid-endothelial interactions in the innate immune response to adenovirus vectors [J].
Liu, Q ;
Zaiss, AK ;
Colarusso, P ;
Patel, K ;
Haljan, G ;
Wickham, TJ ;
Muruve, DA .
HUMAN GENE THERAPY, 2003, 14 (07) :627-643
[27]   Pulmonary inflammation induced by incomplete or inactivated adenoviral particles [J].
McCoy, RD ;
Davidson, BL ;
Roessler, BJ ;
Huffnagle, GB ;
Janich, SL ;
Laing, TJ ;
Simon, RH .
HUMAN GENE THERAPY, 1995, 6 (12) :1553-1560
[28]   Adenoviral gene therapy leads to rapid induction of multiple chemokines and acute neutrophil-dependent hepatic injury in vivo [J].
Muruve, DA ;
Barnes, MJ ;
Stillman, IE ;
Libermann, TA .
HUMAN GENE THERAPY, 1999, 10 (06) :965-976
[29]   Role of αv integrins in adenovirus cell entry and gene delivery [J].
Nemerow, GR ;
Stewart, PL .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1999, 63 (03) :725-+
[30]   Nonspecific inflammation inhibits adenovirus-mediated pulmonary gene transfer and expression independent of specific acquired immune responses [J].
Otake, K ;
Ennist, DL ;
Harrod, K ;
Trapnell, BC .
HUMAN GENE THERAPY, 1998, 9 (15) :2207-2222