Simon Emily J, Howells Morgan A, Stuart Johnasha D, Boehme Karl W
Department of Microbiology and Immunology and Center for Microbial Pathogenesis and Host Inflammatory Response, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Viruses. 2017 Jun 6;9(6):140. doi: 10.3390/v9060140.
Reovirus is under development as a therapeutic for numerous types of cancer. In contrast to other oncolytic viruses, the safety and efficacy of reovirus have not been improved through genetic manipulation. Here, we tested the oncolytic capacity of recombinant strains (rs) of prototype reovirus laboratory strains T1L and T3D (rsT1L and rsT3D, respectively) in a panel of non-small cell lung cancer (NSCLC) cell lines. We found that rsT1L was markedly more cytolytic than rsT3D in the large cell carcinoma cell lines tested, whereas killing of adenocarcinoma cell lines was comparable between rsT1L and rsT3D. Importantly, non-recombinant T1L and T3D phenocopied the kinetics and magnitude of cell death induced by recombinant strains. We identified gene segments L2, L3, and M1 as viral determinants of strain-specific differences cell killing of the large cell carcinoma cell lines. Together, these results indicate that recombinant reoviruses recapitulate the cell killing properties of non-recombinant, tissue culture-passaged strains. These studies provide a baseline for the use of reverse genetics with the specific objective of engineering more effective reovirus oncolytics. This work raises the possibility that type 1 reoviruses may have the capacity to serve as more effective oncolytics than type 3 reoviruses in some tumor types.
呼肠孤病毒正作为多种癌症的治疗药物进行研发。与其他溶瘤病毒不同,呼肠孤病毒的安全性和有效性尚未通过基因操作得到改善。在此,我们在一组非小细胞肺癌(NSCLC)细胞系中测试了原型呼肠孤病毒实验室菌株T1L和T3D的重组菌株(分别为rsT1L和rsT3D)的溶瘤能力。我们发现,在所测试的大细胞癌细胞系中,rsT1L的细胞溶解能力明显强于rsT3D,而在腺癌细胞系中,rsT1L和rsT3D的杀伤能力相当。重要的是,非重组T1L和T3D复制了重组菌株诱导的细胞死亡的动力学和程度。我们将基因片段L2、L3和M1确定为大细胞癌细胞系中菌株特异性细胞杀伤差异的病毒决定因素。总之,这些结果表明重组呼肠孤病毒概括了非重组、组织培养传代菌株的细胞杀伤特性。这些研究为使用反向遗传学以设计更有效的呼肠孤病毒溶瘤剂这一特定目标提供了基线。这项工作提出了1型呼肠孤病毒在某些肿瘤类型中可能比3型呼肠孤病毒更有效地作为溶瘤剂的可能性。