Liu Guei-Sheung, Wang Jiang-Hui, Lee Jia Hui, Tsai Pei-Jhen, Tsai Han-En, Sheu Shwu-Jiuan, Lin Hsiu-Chen, Dusting Gregory J, Tai Ming-Hong, Bee Youn-Shen
Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
Ophthalmology, Department of Surgery, University of Melbourne, East Melbourne, Victoria, Australia.
PLoS One. 2015 Dec 7;10(12):e0143956. doi: 10.1371/journal.pone.0143956. eCollection 2015.
Subconjunctival injection is a minimally invasive route for gene delivery to ocular tissues, but has traditionally been limited to use in the cornea. The accurate ocular distribution of virus has not, however, been previously investigated. Adenovirus is an attractive gene vector as it can deliver large genes and allow for short-term gene expression, but how safe it is when delivered via subconjunctival injection remains to be established. We have characterized the bio-distribution and safety of subconjunctivally administered adenovirus in Brown Norway rats. The bio-distribution and transgene duration of adenovirus carrying luciferase gene (Ad-Luci) at various time intervals were evaluated via bioluminescence imaging after subconjunctival injection. Adenovirus carrying a reporter gene, β-galactosidase (Ad-LacZ) or hrGFP (Ad-hrGFP) was administered subconjunctivally and the viral distribution in various ocular tissues was assessed by histological analysis and quantitative PCR (qPCR). Hepatic damage was assessed by biochemical and immunohistological analysis with TUNEL stain. Systemic immunogenicity was assessed by measuring serum level of TNF-α via ELISA, 2 hours and 14 days after administration of adenovirus. Retinal function was examined by electroretinography. Subconjunctival injection of Ad-Luci induced luciferase expression in the injected eyes within 24 hours, for at least 64 days. Histological analysis showed adenovirus distributed across anterior and posterior ocular tissues. qPCR demonstrated different amounts of adenovirus in different ocular tissues, with the highest amounts closest to the injection site Unlike the intravenous route, subconjunctivally delivered adenovirus did not elicit any detectable hepatic injury or systemic immunogenicity. Retinal function was unaffected by adenovirus irrespective of administration route. In conclusion, an adenoviral vector administered subconjunctivally can infiltrate into different ocular tissues and lead to short-term ocular transgene expression, without causing hepatic injury and immune activation. Therefore, subconjunctivally administered adenovirus may be a promising gene delivery approach for managing anterior and posterior segment eye diseases requiring short-term therapy.
结膜下注射是一种将基因递送至眼组织的微创途径,但传统上仅限于在角膜中使用。然而,病毒在眼内的准确分布此前尚未得到研究。腺病毒是一种有吸引力的基因载体,因为它可以递送大基因并实现短期基因表达,但通过结膜下注射给药时其安全性仍有待确定。我们已经对在棕色挪威大鼠中结膜下给药的腺病毒的生物分布和安全性进行了表征。结膜下注射后,通过生物发光成像评估携带荧光素酶基因(Ad-Luci)的腺病毒在不同时间间隔的生物分布和转基因持续时间。结膜下给予携带报告基因β-半乳糖苷酶(Ad-LacZ)或人重组绿色荧光蛋白(Ad-hrGFP)的腺病毒,并通过组织学分析和定量PCR(qPCR)评估病毒在各种眼组织中的分布。通过生化分析、免疫组织学分析以及TUNEL染色评估肝损伤。通过ELISA在腺病毒给药后2小时和14天测量血清TNF-α水平来评估全身免疫原性。通过视网膜电图检查视网膜功能。结膜下注射Ad-Luci可在24小时内在注射眼中诱导荧光素酶表达,持续至少64天。组织学分析表明腺病毒分布于眼前段和眼后段组织。qPCR显示不同眼组织中的腺病毒量不同,最高量最接近注射部位。与静脉内途径不同,结膜下递送的腺病毒未引起任何可检测到的肝损伤或全身免疫原性。无论给药途径如何,视网膜功能均不受腺病毒影响。总之,结膜下给药的腺病毒载体可渗入不同的眼组织并导致短期眼内转基因表达,而不会引起肝损伤和免疫激活。因此,结膜下给药的腺病毒可能是一种有前景的基因递送方法,可用于治疗需要短期治疗的眼前段和眼后段眼病。