Quantitative model demonstrating that recombinant adeno-associated virus and green fluorescent protein are non-toxic to the rat retina

被引:13
作者
Daniels, DM [1 ]
Shen, WY [1 ]
Constable, IJ [1 ]
Rakoczy, PE [1 ]
机构
[1] Univ Western Australia, Ctr Ophthalmol & Visual Sci, Perth, WA 6009, Australia
关键词
histology; rAAV; gene therapy; retina;
D O I
10.1046/j.1442-9071.2003.00693.x
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background: Recombinant adeno-associated virus (rAAV) is one of the most promising recombinant viral vectors for delivering therapeutic agents to the retina. The present study aims to quantify any effect that an rAAV construct may have on the retina. To be able to use rAAV for therapeutic purposes, the potentially toxic effect of the vector and an associated green fluorescent protein (gfp) marker has to be investigated. Methods: By combining histological analysis with computer scanning techniques, the local toxicity of rAAV and gfp can be measured. This will have obvious implications for its role as a carrier in the rapidly developing world of gene therapy. Results: It is shown that a construct consisting of rAAV and gfp, delivered subretinally to rat eyes, causes no more histological damage than injection with saline alone. Furthermore, via fluorescent fundus photography and computer scanning techniques it is seen that the area exposed to the rAAV-gfp construct is significantly greater than the area of histological change. Conclusions: It is thus concluded that the rAAV-gfp construct has no significant toxic effect, at an anatomical level, on the retina 12 months after injection.
引用
收藏
页码:439 / 444
页数:6
相关论文
共 23 条
  • [1] Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina
    Bennett, J
    Maguire, AM
    Cideciyan, AV
    Schnell, M
    Glover, E
    Anand, V
    Aleman, TS
    Chirmule, N
    Gupta, AR
    Huang, YJ
    Gao, GP
    Nyberg, WC
    Tazelaar, J
    Hughes, J
    Wilson, JM
    Jacobson, SG
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (17) : 9920 - 9925
  • [2] Bennett J, 1997, INVEST OPHTH VIS SCI, V38, P2857
  • [3] BERNS KI, 1994, ANN NY ACAD SCI, V27, P95
  • [4] Observed incidence of tumorigenesis in long-term rodent studies of rAAV vectors
    Donsante, A
    Vogler, C
    Muzyczka, N
    Crawford, JM
    Barker, J
    Flotte, T
    Campbell-Thompson, M
    Daly, T
    Sands, MS
    [J]. GENE THERAPY, 2001, 8 (17) : 1343 - 1346
  • [5] Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virus
    Flannery, JG
    Zolotukhin, S
    Vaquero, MI
    LaVail, MM
    Muzyczka, N
    Hauswirth, WW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (13) : 6916 - 6921
  • [6] FLOTTE TR, 1995, GENE THER, V2, P357
  • [7] Flotte TR, 2001, CURR OPIN MOL THER, V3, P497
  • [8] Adeno-associated virus vector-mediated IL-10 gene delivery prevents type 1 diabetes in NOD mice
    Goudy, K
    Song, SH
    Wasserfall, C
    Zhang, YC
    Kapturczak, M
    Muir, A
    Powers, M
    Scott-Jorgensen, M
    Campbell-Thompson, M
    Crawford, JM
    Ellis, TM
    Flotte, TR
    Atkinson, MA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) : 13913 - 13918
  • [9] Hunt S, 2001, CURR OPIN MOL THER, V3, P509
  • [10] PROSPECTS FOR THE USE OF ADENOASSOCIATED VIRUS AS A VECTOR FOR HUMAN GENE-THERAPY
    KOTIN, RM
    [J]. HUMAN GENE THERAPY, 1994, 5 (07) : 793 - 801