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首页> 外文期刊>Human gene therapy. Clinical development >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Toca 511的静脉内给药证明了原位免疫感受态小鼠神经胶质瘤模型的治疗功效

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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),一种非溶性,两性逆转录病毒复制载体(RRV),编码并向肿瘤传递功能优化的酵母胞嘧啶脱氨酶(CD)基因。在用Toca 511和5-氟胞嘧啶(5-FC)处理的原位神经胶质瘤模型中,感染细胞内的CD酶将5-FC转化为5-氟尿嘧啶(5-FU),从而杀死了肿瘤。目前正在对复发性高级别胶质瘤(HGG)患者进行临床研究,即通过肿瘤内注射或通过注射入切除床局部递送的Toca 511以及随后的口服缓释5-FC(Toca FC)。如果可行的话,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类型的肿瘤。在这里,我们介绍了支持静脉给药方案发展的临床前数据。首先,我们表明在临床前模型中静脉内施用Toca 511不会导致RVV的广泛复制或不受控制的复制。施用Toca 511后180天,血液和大部分组织中均未发现或存在低病毒DNA。我们还显示静脉内施用RRV可以有效感染并传播带有绿色荧光蛋白(GFP)编码基因(Toca GFP)的载体通过免疫功能和免疫功能低下的动物模型中的肿瘤。但是,肿瘤内的初始载体定位似乎取决于给药方式。当将Toca 511静脉内或颅内联合5-FC治疗时,可在具有免疫能力的小鼠中观察到长期存活,并且该组合在临床前模型中具有良好的耐受性。在预先存在对载体的免疫应答的动物中,也可以提高存活率,从而支持重复给药的潜力。基于这些和其他支持性数据,目前正在研究一项临床试验,该试验研究静脉注射To​​ca 511对HGG复发患者的作用。

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