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Prolonged transgene expression with lentiviral vectors in the aqueous humor outflow pathway of nonhuman primates.

机译:慢病毒载体在非人类灵长类动物房水流出途径中的转基因表达延长。

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We injected lentiviral vectors into the eyes of live nonhuman primates to assess potential for glaucoma gene therapy. Anterior chambers of five cynomolgus monkeys were injected with green fluorescent protein (GFP)-encoding feline immunodeficiency viral vectors. The monkeys were monitored for in vivo transgene expression and clinical parameters. Their eyes were harvested 2-15 months postinjection for tissue analyses. All seven eyes injected with 1.0-2.0 x 10(8) transducing units (TU) showed substantial GFP fluorescence in the trabecular meshwork (TM), which was observable even by goniophotographic monitoring for up to 15 months. Only the lowest dose (0.03 x 10(8) TU) failed to result in TM fluorescence detectable in vivo, and five of the eight vector-injected eyes continued to display substantial GFP expression when enucleated eyes were examined at 2, 7, or 15 months postinjection. Some transduced cells were also detected in the iris and ciliary body. Mild, transient postinjection inflammatory responsesexceeding that induced by a control saline injection were observed, but vectors did not raise intraocular pressure and were well tolerated. The results demonstrate the first lentiviral vector transduction of the nonhuman primate aqueous humor outflow pathway and support application of the system to human glaucoma gene therapy.
机译:我们将慢病毒载体注射到活的非人类灵长类动物的眼睛中,以评估青光眼基因治疗的潜力。向五只食蟹猴的前房注射编码绿色荧光蛋白(GFP)的猫免疫缺陷病毒载体。监测猴子的体内转基因表达和临床参数。注射后2-15个月,收集他们的眼睛进行组织分析。注射1.0-2.0 x 10(8)转换单元(TU)的所有七只眼睛在小梁网(TM)中均显示出大量的GFP荧光,甚至通过长达15个月的眼底照相监视也可以观察到。只有最低剂量(0.03 x 10(8)TU)不能导致在体内可检测到TM荧光,并且当在2、7或15点检查去核眼时,八只载体注射的眼睛中有五只继续显示大量的GFP表达。注射后数月。在虹膜和睫状体中也检测到一些转导的细胞。观察到轻度的,短暂的注射后炎症反应,超过了对照盐水注射所诱导的炎症反应,但是载体没有升高眼内压并且被很好地耐受。结果证明了非人灵长类动物房水流出途径的第一个慢病毒载体转导,并支持该系统在人青光眼基因治疗中的应用。

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