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首页> 外文期刊>Human gene therapy >Intravenous Administration of Retroviral Replicating Vector, Toca 511, Demonstrates Therapeutic Efficacy in Orthotopic Immune-Competent Mouse Glioma Model
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Intravenous Administration of Retroviral Replicating Vector, Toca 511, Demonstrates Therapeutic Efficacy in Orthotopic Immune-Competent Mouse Glioma Model

机译:逆转录病毒复制载体的静脉内施用TOCA 511,证明了原位免疫司马小鼠胶质瘤模型中的治疗效果

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摘要

Toca 511 (vocimagene amiretrorepvec), a nonlytic, amphotropic retroviral replicating vector (RRV), encodes and delivers a functionally optimized yeast cytosine deaminase (CD) gene to tumors. In orthotopic glioma models treated with Toca 511 and 5-fluorocytosine (5-FC) the CD enzyme within infected cells converts 5-FC to 5-fluorouracil (5-FU), resulting in tumor killing. Toca 511, delivered locally either by intratumoral injection or by injection into the resection bed, in combination with subsequent oral extended-release 5-FC (Toca FC), is under clinical investigation in patients with recurrent high-grade glioma (HGG). If feasible, intravenous administration of vectors is less invasive, can easily be repeated if desired, and may be applicable to other tumor types. Here, we present preclinical data that support the development of an intravenous administration protocol. First we show that intravenous administration of Toca 511 in a preclinical model did not lead to widespread or uncontrolled replication of the RVV. No, or low, viral DNA was found in the blood and most of the tissues examined 180 days after Toca 511 administration. We also show that RRV administered intravenously leads to efficient infection and spread of the vector carrying the green fluorescent protein (GFP)-encoding gene (Toca GFP) through tumors in both immune-competent and immune-compromised animal models. However, initial vector localization within the tumor appeared to depend on the mode of administration. Long-term survival was observed in immune-competent mice when Toca 511 was administered intravenously or intracranially in combination with 5-FC treatment, and this combination was well tolerated in the preclinical models. Enhanced survival could also be achieved in animals with preexisting immune response to vector, supporting the potential for repeated administration. On the basis of these and other supporting data, a clinical trial investigating intravenous administration of Toca 511 in patients with recurrent HGG is currently open and enrolling.
机译:TOCA 511(Vocimagene AmiretrorePvec),非贱金属逆转录病毒复制载体(RRV),编码并传递功能优化的酵母胞嘧啶脱氨酶(CD)基因对肿瘤。在用TOCA 511和5-氟核(5-FC)处理的原位胶质瘤模型中,感染细胞内的CD酶转化为5-Fc至5-氟尿嘧啶(5-FU),导致肿瘤杀伤。通过肿瘤内注射或注射进食床,与随后的口腔延长 - 发布5-Fc(TOCA FC)组合,局部递送TOCA 511,该临床调查是患有复发性高等胶质瘤(HGG)的临床调查。如果可行,静脉内施用载体的侵入性较小,如果需要,可以容易地重复,并且可以适用于其他肿瘤类型。在这里,我们呈现了支持静脉内给药方案的发展的临床前数据。首先,我们表明,临床前模型中的TOCA 511静脉内施用不会导致RVV的广泛或不受控制的复制。在血液中没有发现缺血和低,病毒DNA,在TOCA 511给药后180天检查了大部分组织。我们还表明RRV静脉内施用,通过免疫司令和免疫受损动物模型中的肿瘤,高效地导致携带绿色荧光蛋白(GFP)的载体(TOCA GFP)的载体传播。然而,肿瘤内的初始载体定位似乎取决于给药方式。当TOCA 511与5-FC处理组合施用TOCA 511时,在免疫富集的小鼠中观察到长期存活,并且这种组合在临床前模型中良好耐受。在具有预先存在的免疫应答对载体的动物中也可以实现增强的存活,支持反复给药的可能性。在这些和其他支持数据的基础上,研究临床试验在经常性HGG患者中静脉内施用TOCA 511的临床试验目前正在开放和注册。

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