Department of Gene Therapy and Regenerative Medicine, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8544, Japan.
South Kyushu Center for Innovative Medical Research and Application, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8544, Japan.
Viruses. 2021 Dec 14;13(12):2502. doi: 10.3390/v13122502.
Gene therapy is currently in the public spotlight. Several gene therapy products, including oncolytic virus (OV), which predominantly replicates in and kills cancer cells, and COVID-19 vaccines have recently been commercialized. Recombinant adenoviruses, including replication-defective adenoviral vector and conditionally replicating adenovirus (CRA; oncolytic adenovirus), have been extensively studied and used in clinical trials for cancer and vaccines. Here, we review the biology of wild-type adenoviruses, the methodological principle for constructing recombinant adenoviruses, therapeutic applications of recombinant adenoviruses, and new technologies in pluripotent stem cell (PSC)-based regenerative medicine. Moreover, this article describes the technology platform for efficient construction of diverse "CRAs that can specifically target tumors with multiple factors" (m-CRAs). This technology allows for modification of four parts in the adenoviral E1 region and the subsequent insertion of a therapeutic gene and promoter to enhance cancer-specific viral replication (i.e., safety) as well as therapeutic effects. The screening study using the m-CRA technology successfully identified survivin-responsive m-CRA (Surv.m-CRA) as among the best m-CRAs, and clinical trials of Surv.m-CRA are underway for patients with cancer. This article also describes new recombinant adenovirus-based technologies for solving issues in PSC-based regenerative medicine.
基因治疗目前备受关注。最近,已有几种基因治疗产品(包括溶瘤病毒(OV),其主要在癌细胞内复制并杀死癌细胞,以及 COVID-19 疫苗)实现商业化。复制缺陷型腺病毒载体和条件复制型腺病毒(CRA;溶瘤腺病毒)等重组腺病毒已被广泛研究并用于癌症和疫苗的临床试验。在这里,我们回顾了野生型腺病毒的生物学特性、构建重组腺病毒的方法学原理、重组腺病毒的治疗应用以及基于多能干细胞(PSC)的再生医学中的新技术。此外,本文描述了高效构建多种“可特异性靶向多种因素肿瘤的 CRA”(m-CRA)的技术平台。该技术允许对腺病毒 E1 区域的四个部分进行修饰,并随后插入治疗基因和启动子,以增强肿瘤特异性病毒复制(即安全性)和治疗效果。使用 m-CRA 技术的筛选研究成功鉴定出对生存素反应的 m-CRA(Surv.m-CRA)作为最佳 m-CRA 之一,目前正在对癌症患者进行 Surv.m-CRA 的临床试验。本文还介绍了基于重组腺病毒的新技术,用于解决基于 PSC 的再生医学中的问题。