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Highlights of the inaugural ten – the launch of Neuro-Oncology Advances

机译:首届十大亮点–神经肿瘤学进展的启动

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摘要

Oncolytic viral-based therapies are gaining increasing attention as a promising therapeutic approach for high-grade gliomas. Converging evidence suggests the possibility of an anti-tumoral immune response that is responsible for tumor eradication, leaving room for immune activation as a synergistic treatment option . In this issue, Rivera-Molina . report on the utility of the clinical-trial tested oncolytic Delta-24-RGD virus that is engineered to be armed with a positive activator of the tumor necrosis factor receptor superfamily synapsis: GITRL/GITR . The authors demonstrate increased recruitment and activation of T-cells in tumors of mice treated with the armed oncolytic antivirus, dubbed Delta-24-GREAT, with associated improved survival in comparison to mice treated with Delta-24-RGD alone. Histopathological examination demonstrated extensive necrosis within Delta-24-GREAT treated tissue. The results of this study highlight an opportunity to overcome the intrinsic lack of co-stimulatory molecules in cancer cells to trigger robust immune responses in high-grade gliomas. The complement of available T-cell activators may be exploited in future studies to achieve synergistic anti-neoplastic effects in glioblastoma with hopes of rapid translation of armed viruses into controlled clinical trials.
机译:溶瘤病毒为基础的治疗方法作为高级别神经胶质瘤的一种有前途的治疗方法正受到越来越多的关注。越来越多的证据表明,抗肿瘤免疫反应可能会根除肿瘤,从而为协同治疗选择留下了激活免疫的空间。在本期中,Rivera-Molina。报告了经临床试验测试的溶瘤Delta-24-RGD病毒的实用性,该病毒经工程改造可配备肿瘤坏死因子受体超家族突触的阳性激活剂GITRL / GITR。作者证明,与单独使用Delta-24-RGD治疗的小鼠相比,用武装溶瘤抗病毒剂Delta-24-GREAT治疗的小鼠的肿瘤中T细胞的募集和激活增加,并具有改善的存活率。组织病理学检查显示在Delta-24-GREAT处理的组织内广泛坏死。这项研究的结果凸显了一个机会,可以克服癌细胞中固有的共刺激分子的缺乏,从而引发高级神经胶质瘤中强大的免疫反应。将来的研究中可能会利用现有T细胞激活剂的补体,以在胶质母细胞瘤中实现协同抗肿瘤作用,希望将武装病毒快速转化为受控临床试验。

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