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

机译:定量模型证明重组腺相关病毒和绿色荧光蛋白对大鼠视网膜无毒。

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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.
机译:背景:重组腺相关病毒(rAAV)是最有前途的重组病毒载体之一,可将治疗剂递送至视网膜。本研究旨在量化rAAV构建体可能对视网膜产生的任何影响。为了能够将rAAV用于治疗目的,必须研究载体和相关绿色荧光蛋白(gfp)标记的潜在毒性作用。方法:结合组织学分析和计算机扫描技术,可以测定rAAV和gfp的局部毒性。这将对其在迅速发展的基因治疗领域中作为载体的作用产生明显影响。结果:显示了由rAAV和gfp组成的构建体,其视网膜下递送至大鼠眼睛,与仅注射盐水相比,没有引起更多的组织学损伤。此外,通过荧光眼底照相和计算机扫描技术,可以看出暴露于rAAV-gfp构建体的面积显着大于组织学变化的面积。结论:因此得出结论,注射后12个月,rAAV-gfp构建体在解剖学上对视网膜没有明显的毒性作用。

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