Suppr超能文献

腺病毒生物学、重组腺病毒和腺病毒在基因治疗中的应用。

Adenovirus Biology, Recombinant Adenovirus, and Adenovirus Usage in Gene Therapy.

机构信息

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.

出版信息

Viruses. 2021 Dec 14;13(12):2502. doi: 10.3390/v13122502.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8499/8706629/848e0d942f78/viruses-13-02502-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验