Department of Microbiology and Molecular Genetics, Mie University Graduate School of Medicine, Tsu, Japan.
Research Centre for Development of Recombinant VLP Vaccines, Research Institutes of Excellence, Mie University, Tsu, Japan.
Rev Med Virol. 2024 Nov;34(6):e70008. doi: 10.1002/rmv.70008.
Human parainfluenza virus type 2 (hPIV2), one of the causative agents of infantile common cold, is a non-segmented negative-sense RNA virus with a robust gene expression system. It infects recurrently throughout human life without causing severe disease. Because hPIV2 has a viral envelope that can carry ectopic proteins, we developed a non-propagative RNA/protein-carrying vector BC-PIV by deleting the F gene from hPIV2. BC-PIV can be vigorously proliferated in the stable packaging cell line Vero/BC-F cells expressing the hPIV2 F gene but not in other cells. BC-PIV can deliver exogenous gene(s) on a multigenic RNA genome as an inserted gene fragment(s) and simultaneously deliver exogenous protein(s) on its envelope in a membrane-anchored form. For example, influenza virus M2e protein, Ebola virus GP protein, and severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) spike protein were shown to be highly expressed in packaging cells and incorporated into the virion. The Ebola virus GP protein and SARS-CoV-2 spike protein, each delivered via BC-PIV, efficiently induced neutralising antibodies against each virus, even after prior treatment with recombinant BC-PIV in mice and hamsters, respectively. In this review, we describe the properties of BC-PIV as a promising vaccine vector, and also demonstrate its application as an anti-tumour virus.
人副流感病毒 2 型(hPIV2)是婴幼儿普通感冒的病原体之一,是一种具有强大基因表达系统的非节段性负义 RNA 病毒。它在人类生命中反复感染而不引起严重疾病。由于 hPIV2 具有可以携带异位蛋白的病毒包膜,我们通过从 hPIV2 中删除 F 基因来开发了一种非增殖性 RNA/蛋白携带载体 BC-PIV。BC-PIV 可以在稳定表达 hPIV2 F 基因的包装细胞系 Vero/BC-F 中大量增殖,但不能在其他细胞中增殖。BC-PIV 可以将外源基因(多个基因的 RNA 基因组上的插入基因片段)作为插入基因片段,同时将包膜上的外源蛋白(以膜锚定形式)递送到病毒中。例如,流感病毒 M2e 蛋白、埃博拉病毒 GP 蛋白和严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突蛋白在包装细胞中被高度表达并整合到病毒粒子中。通过 BC-PIV 递送的埃博拉病毒 GP 蛋白和 SARS-CoV-2 刺突蛋白分别在小鼠和仓鼠中预先用重组 BC-PIV 处理后,有效地诱导了针对每种病毒的中和抗体。在这篇综述中,我们描述了 BC-PIV 作为一种有前途的疫苗载体的特性,并展示了它作为抗肿瘤病毒的应用。