Rosewell Shaw Amanda, Suzuki Masataka
Department of Medicine, Baylor College of Medicine, Houston, TX, USA; Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, TX, USA.
Department of Medicine, Baylor College of Medicine, Houston, TX, USA; Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, TX, USA.
Curr Opin Virol. 2016 Dec;21:9-15. doi: 10.1016/j.coviro.2016.06.009. Epub 2016 Jul 2.
Oncolytic adenoviruses (Onc.Ads) selectively replicate in and lyse cancer cells and are therefore commonly used vectors in clinical trials for cancer gene therapy. Building upon the well-characterized adenoviral natural tropism, genetic modification of Onc.Ad can enhance/regulate their transduction and replication within specific cancer cell types. However, Onc.Ad-mediated tumor cell lysis cannot fully eliminate tumors. The hostile tumor microenvironment provides many barriers to efficient oncolytic virotherapy, as tumors develop structure and immune-evasion mechanisms in order to grow and ultimately spread. For these reasons, Onc.Ads modified to deliver structural or immune modulatory molecules (Armed Onc.Ads) have been developed to overcome the physical and immunological barriers of solid tumors. The combination of oncolysis with tumor microenvironment modulation/destruction may provide a promising platform for Ad-based cancer gene therapy.
溶瘤腺病毒(Onc.Ads)可在癌细胞中选择性复制并裂解癌细胞,因此是癌症基因治疗临床试验中常用的载体。基于已充分表征的腺病毒天然嗜性,对溶瘤腺病毒进行基因改造可增强/调节其在特定癌细胞类型中的转导和复制。然而,溶瘤腺病毒介导的肿瘤细胞裂解并不能完全消除肿瘤。恶劣的肿瘤微环境为有效的溶瘤病毒疗法提供了许多障碍,因为肿瘤会形成结构和免疫逃避机制以实现生长并最终扩散。出于这些原因,已开发出经过改造以递送结构或免疫调节分子的溶瘤腺病毒(武装溶瘤腺病毒),以克服实体瘤的物理和免疫屏障。溶瘤作用与肿瘤微环境调节/破坏的结合可能为基于腺病毒的癌症基因治疗提供一个有前景的平台。