Hamdan Firas, Martins Beatriz, Feodoroff Michaela, Giannoula Yvonne, Feola Sara, Fusciello Manlio, Chiaro Jacopo, Antignani Gabriella, Grönholm Mikaela, Ylösmäki Erkko, Cerullo Vincenzo
Laboratory of Immunovirotherapy (IVTLab), Drug Research Program, Faculty of Pharmacy, University of Helsinki, Viikinkaari 5E, 00790 Helsinki, Finland.
Drug Research Program, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, Helsinki, Finland.
Mol Ther Methods Clin Dev. 2021 Feb 4;20:625-634. doi: 10.1016/j.omtm.2021.01.014. eCollection 2021 Mar 12.
Oncolytic adenoviruses have become ideal agents in the path toward treating cancer. Such viruses have been engineered to conditionally replicate in malignant cells in which certain signaling pathways have been disrupted. Other than such oncolytic properties, the viruses need to activate the immune system in order to sustain a long-term response. Therefore, oncolytic adenoviruses have been genetically modified to express various immune-stimulatory agents to achieve this. However, genetically modifying adenoviruses is very time consuming and labor intensive with the current available methods. In this paper, we describe a novel method we have called GAMER-Ad to genetically modify adenovirus genomes within 2 days. Our method entails the replacement of the gp19k gene in the E3 region with any given gene of interest (GOI) using Gibson Assembly avoiding the homologous recombination between the shuttle and the parental plasmid. In this manuscript as proof of concept we constructed and characterized three oncolytic adenoviruses expressing CXCL9, CXCL10, and interleukin-15 (IL-15). We demonstrate that our novel method is fast, reliable, and simple compared to other methods. We anticipate that our method will be used in the future to genetically engineer oncolytic but also other adenoviruses used for gene therapy as well.
溶瘤腺病毒已成为癌症治疗道路上的理想药物。这类病毒经过改造,可在某些信号通路被破坏的恶性细胞中进行条件性复制。除了这种溶瘤特性外,病毒还需要激活免疫系统以维持长期反应。因此,溶瘤腺病毒已被基因改造以表达各种免疫刺激剂来实现这一点。然而,使用现有的方法对腺病毒进行基因改造非常耗时且费力。在本文中,我们描述了一种我们称为GAMER-Ad的新方法,可在两天内对腺病毒基因组进行基因改造。我们的方法是使用吉布森组装法,用任何给定的感兴趣基因(GOI)替换E3区域中的gp19k基因,避免穿梭质粒与亲本质粒之间的同源重组。在本手稿中,作为概念验证,我们构建并表征了三种表达CXCL9、CXCL10和白细胞介素-15(IL-15)的溶瘤腺病毒。我们证明,与其他方法相比,我们的新方法快速、可靠且简单。我们预计,我们的方法未来将用于对溶瘤腺病毒以及其他用于基因治疗的腺病毒进行基因工程改造。