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Evaluation Of Ires-Mediated Cell Type-Specific Cytotoxicity Of Poliovirus Using A Colorimetric Cell Proliferation Assay

机译:使用比色细胞增殖检测评估脊髓灰质炎病毒介导的细胞类型特异性细胞毒性

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摘要

PVS-RIPO is a recombinant oncolytic poliovirus designed for clinical application to target CD155 expressing malignant gliomas and other malignant diseases. PVS-RIPO does not replicate in healthy neurons and is therefore non-pathogenic in rodent and non-human primate models of poliomyelitis. A tetrazolium salt dye-based cellular assay was developed and qualified to define the cytotoxicity of virus preparations on susceptible cells and to explore the target cell specificity of PVS-RIPO. In this assay, PVS-RIPO inhibited proliferation of U87-MG astrocytoma cells in a dose-dependent manner. However, HEK293 cells were much less susceptible to cell killing by PVS-RIPO. In contrast, the Sabin type 1 live attenuated poliovirus vaccine strain (PV(1)S) was cytotoxic to both HEK293 and U87-MG cells. The correlation between expression of CD155 and cytotoxicity was also explored using six different cell lines. There was little or no expression of CD155 and PVS-RIPO-induced cytotoxicity in Jurkat and Daudi cells. HEK293 was the only cell line tested that showed CD155 expression and resistance to PVS-RIPO cytotoxicity. The results indicate that differential cytotoxicity measured by the colorimetric assay can be used to evaluate the cytotoxicity and cell-type specificity of recombinant strains of poliovirus and to demonstrate lot to lot consistency during the manufacture of viruses intended for clinical use.
机译:PVS-RIPO是一种重组溶瘤脊髓灰质炎病毒,设计用于临床应用,以靶向表达CD155的恶性神经胶质瘤和其他恶性疾病。 PVS-RIPO在健康神经元中不复制,因此在脊髓灰质炎的啮齿动物和非人类灵长类动物模型中没有致病性。开发了一种基于四唑盐染料的细胞分析方法,该方法可用于定义病毒制剂对易感细胞的细胞毒性,并探索PVS-RIPO的靶细胞特异性。在该测定中,PVS-RIPO以剂量依赖的方式抑制U87-MG星形细胞瘤细胞的增殖。但是,HEK293细胞不易被PVS-RIPO杀死。相反,萨宾1型减毒脊髓灰质炎活疫苗株(PV(1)S)对HEK293细胞和U87-MG细胞均具有细胞毒性。还使用六种不同的细胞系探索了CD155表达与细胞毒性之间的相关性。在Jurkat和Daudi细胞中几乎没有CD155和PVS-RIPO诱导的细胞毒性表达。 HEK293是测试的唯一显示CD155表达和对PVS-RIPO细胞毒性抗性的细胞系。结果表明,通过比色测定法测量的差异细胞毒性可用于评估脊髓灰质炎病毒重组株的细胞毒性和细胞类型特异性,并证明在生产用于临床用途的病毒期间批次之间的一致性。

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