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短暂免疫抑制可阻止兔视网膜中病毒转导的增强型绿色荧光蛋白被排斥。

Transient immunosuppression stops rejection of virus-transduced enhanced green fluorescent protein in rabbit retina.

作者信息

Doi Kentaro, Kong Jian, Hargitai Janos, Goff Stephen P, Gouras Peter

机构信息

Department of Ophthalmology, College of Physicians & Surgeons, Columbia University, 630 W. 168th St., New York, NY 10032, USA.

出版信息

J Virol. 2004 Oct;78(20):11327-33. doi: 10.1128/JVI.78.20.11327-11333.2004.

Abstract

The expression of lentivirus-transduced enhanced green fluorescent protein (EGFP) was detectable in rabbit retinal pigment epithelium (RPE) within 3 to 5 days after subretinal injection of the vector. Within 2 to 3 weeks, EGFP-expressing cells were eliminated by rejection. In the current experiments, we monitor serum antibody titers for EGFP before and after transduction and determine whether systemic immunosuppression prevents recognition of EGFP by the immune system. While all control rabbits developed antibodies against EFGP and showed signs of rejection, no such evidence was observed with animals which received immunosuppression. One month of systemic immunosuppression permanently prevented rejection of RPE with EGFP expression. Fluorescence has been maintained for more than a year. If a control eye was injected with the same virus after terminating immunosuppression, both eyes showed signs of rejection. The lack of rejection is not due to tolerance but to a failure of the animals to detect the foreign protein. Detection must depend upon a brief window of time after surgery needed to introduce the vector, perhaps related to a concurrent but transient inflammation. This strategy may be useful in managing other types of rejection in the retina.

摘要

在视网膜下注射载体后的3至5天内,可在兔视网膜色素上皮(RPE)中检测到慢病毒转导的增强型绿色荧光蛋白(EGFP)的表达。在2至3周内,表达EGFP的细胞因排斥反应而被清除。在当前实验中,我们监测转导前后血清中针对EGFP的抗体滴度,并确定全身免疫抑制是否能阻止免疫系统识别EGFP。虽然所有对照兔都产生了针对EFGP的抗体并出现排斥迹象,但接受免疫抑制的动物未观察到此类证据。一个月的全身免疫抑制永久性地阻止了对表达EGFP的RPE的排斥反应。荧光已维持了一年多。如果在终止免疫抑制后给对照眼注射相同的病毒,两只眼睛都会出现排斥迹象。缺乏排斥反应不是由于耐受,而是由于动物未能检测到外源蛋白。检测必须依赖于手术后引入载体所需的短暂时间窗口,这可能与同时发生但短暂的炎症有关。这种策略可能有助于处理视网膜中的其他类型的排斥反应。

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