Successful transgene expression with serial doses of aerosolized rAAV2 vectors in rhesus macaques

被引:34
作者
Fischer, AC
Beck, SE
Smith, CI
Laube, BL
Askin, FB
Guggino, SE
Adams, RJ
Flotte, TR
Guggino, WB
机构
[1] Johns Hopkins Univ, Sch Med, Dept Physiol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pediat Surg, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, Dept Comparat Med, Baltimore, MD 21205 USA
[7] Univ Florida, Dept Pediat, Gainesville, FL 32611 USA
[8] Univ Florida, Powell Gene Therapy Ctr, Gainesville, FL 32611 USA
[9] Drexel Univ, Coll Med, St Christophers Hosp Children, Dept Pediat,Sect Pediat Pulmonol, Philadelphia, PA 19104 USA
关键词
AAV; cystic fibrosis; CFTR; GFP; aerosol; gene therapy; microspraying;
D O I
10.1016/j.ymthe.2003.08.015
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
Bronchoscopic microspraying of recombinant adeno-associated viral (rAAV) vectors targets high doses of vector directly to pulmonary epithelium. Single-dose endobronchial gene therapy trials have been accomplished in cystic fibrosis patients; however, repeated dosing strategies are likely essential for lifetime correction. These studies address whether serial redosing with rAAV2 vectors results in an antiserotypic response and, furthermore, whether it triggers an inflammatory response prohibitive to transgene expression. Serial redosing of 9 x 10(11) infectious units of aerosolized rAAV2 vectors to rhesus macaques resulted in successful gene transfer by quantitative PCR (1.43 x 10(9) copies/g tissue) and transgene expression. Additionally, confocal microscopy and immunohistochemical analysis demonstrated in situ expression localized to the pulmonary epithelium. Although serial redosing did induce a heightened anti-neutralizing antibody response in sera, gene transfer prevailed with resultant expression. This study is the first to demonstrate successful gene transfer subsequent to repeated aerosolized doses of rAAV2 in immunocompetent nonhuman primates without associated inflammatory responses prohibitive to transgene expression.
引用
收藏
页码:918 / 926
页数:9
相关论文
共 30 条
[1]   In vivo model of adeno-associated virus vector persistence and rescue [J].
Afione, SA ;
Conrad, CK ;
Kearns, WG ;
Chunduru, S ;
Adams, R ;
Reynolds, TC ;
Guggino, WB ;
Cutting, GR ;
Carter, BJ ;
Flotte, TR .
JOURNAL OF VIROLOGY, 1996, 70 (05) :3235-3241
[2]   A phase I study of aerosolized administration of tgAAVCF to cystic fibrosis subjects with mild lung disease [J].
Aitken, ML ;
Moss, RB ;
Waltz, DA ;
Dovey, ME ;
Tonelli, MR ;
McNamara, SC ;
Gibson, RL ;
Ramsey, BW ;
Carter, BJ ;
Reynolds, TC .
HUMAN GENE THERAPY, 2001, 12 (15) :1907-1916
[3]   Repeated delivery of adeno-associated virus vectors to the rabbit airway [J].
Beck, SE ;
Jones, LA ;
Chesnut, K ;
Walsh, SM ;
Reynolds, TC ;
Carter, BJ ;
Askin, FB ;
Flotte, TR ;
Guggino, WB .
JOURNAL OF VIROLOGY, 1999, 73 (11) :9446-9455
[4]   Deposition and expression of aerosolized rAAV vectors in the lungs of Rhesus macaques [J].
Beck, SE ;
Laube, BL ;
Barberena, CI ;
Fischer, AC ;
Adams, RJ ;
Chesnut, K ;
Flotte, TR ;
Guggino, WB .
MOLECULAR THERAPY, 2002, 6 (04) :546-554
[5]  
BERNS, 1990, FIELDS VIROLOGY, P1743
[6]   EPIDEMIOLOGY OF ADENOVIRUS-ASSOCIATED VIRUS INFECTION IN A NURSERY POPULATION [J].
BLACKLOW, NR ;
HOGGAN, MD ;
KAPIKIAN, AZ ;
AUSTIN, JB ;
ROWE, WP .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1968, 88 (03) :368-&
[7]  
Carter Barrie J., 1992, Current Opinion in Biotechnology, V3, P533, DOI 10.1016/0958-1669(92)90082-T
[8]   Immune responses to adenovirus and adeno-associated virus in humans [J].
Chirmule, N ;
Propert, KJ ;
Magosin, SA ;
Qian, Y ;
Qian, R ;
Wilson, JM .
GENE THERAPY, 1999, 6 (09) :1574-1583
[9]  
Conrad CK, 1996, GENE THER, V3, P658
[10]  
*CYST FIBR GEN AN, 2002, CFTR MUT TABL