Matsunaga Wataru, Gotoh Akinobu
Joint-Use Research Facilities, Hyogo Medical University, 1-1 Mukogawa, Nishinomiya 663-8501, Japan.
Department of Education for Medical Research Base, Hyogo Medical University, 1-1 Mukogawa, Nishinomiya 663-8501, Japan.
Curr Issues Mol Biol. 2023 Jun 2;45(6):4826-4840. doi: 10.3390/cimb45060307.
Adenoviral vectors, both oncolytic viruses and gene delivery vectors, are among the earliest approved and commercialised vectors for gene therapy. Adenoviruses have high cytotoxicity and immunogenicity. Therefore, lentiviruses or adeno-associated viruses as viral vectors and herpes simplex virus as an oncolytic virus have recently drawn attention. Thus, adenoviral vectors are often considered relatively obsolete. However, their high cargo limit and transduction efficiency are significant advantages over newer viral vectors. This review provides an overview of the new-generation adenoviral vectors. In addition, we describe the modification of the fiber knob region that enhances affinity of adenoviral vectors for cancer cells and the utilisation of cancer-cell-specific promoters to suppress expression of unwanted transgenes in non-malignant tissues.
腺病毒载体,包括溶瘤病毒和基因递送载体,是最早被批准并商业化用于基因治疗的载体之一。腺病毒具有高细胞毒性和免疫原性。因此,慢病毒或腺相关病毒作为病毒载体以及单纯疱疹病毒作为溶瘤病毒最近受到了关注。因此,腺病毒载体常被认为相对过时。然而,它们的高载量限制和转导效率相对于新型病毒载体具有显著优势。本综述概述了新一代腺病毒载体。此外,我们描述了纤维瘤区域的修饰,该修饰增强了腺病毒载体对癌细胞的亲和力,以及利用癌细胞特异性启动子来抑制非恶性组织中不需要的转基因的表达。