Institute of Virology and Immunology IVI, Bern & Mittelhäusern, Switzerland; Institute of Veterinary Bacteriology, University of Bern, Bern, Switzerland; Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, University of Bern, Bern, Switzerland; Department of Veterinary Microbiology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand; Center of Excellence in Emerging Infectious Diseases in Animals, Chulalongkorn University (CU-EIDAs), Bangkok, Thailand.
Department of Vaccinology and Applied Microbiology, Helmholtz Centre for Infection Research (HZI), Braunschweig, Germany.
Nanomedicine. 2023 Apr;49:102655. doi: 10.1016/j.nano.2023.102655. Epub 2023 Jan 18.
Herein, we provide the first description of a synthetic delivery method for self-replicating replicon RNAs (RepRNA) derived from classical swine fever virus (CSFV) using a Coatsome-replicon vehicle based on Coatsome® SS technologies. This results in an unprecedented efficacy when compared to well-established polyplexes, with up to ∼65 fold-increase of the synthesis of RepRNA-encoded gene of interest (GOI). We demonstrated the efficacy of such Coatsome-replicon vehicles for RepRNA-mediated induction of CD8 T-cell responses in mice. Moreover, we provide new insights on physical properties of the RepRNA, showing that the removal of all CSFV structural protein genes has a positive effect on the translation of the GOI. Finally, we successfully engineered RepRNA constructs encoding a porcine reproductive and respiratory syndrome virus (PRRSV) antigen, providing an example of antigen expression with potential application to combat viral diseases. The versatility and simplicity of modifying and manufacturing these Coatsome-replicon vehicle formulations represents a major asset to tackle foreseeable emerging pandemics.
在此,我们提供了一种使用基于 Coatsome® SS 技术的 Coatsome-复制子载体的合成方法,首次对源自经典猪瘟病毒(CSFV)的自我复制复制子 RNA(RepRNA)进行了描述。与成熟的多聚物相比,这导致了前所未有的功效,RepRNA 编码的感兴趣基因(GOI)的合成增加了高达约 65 倍。我们证明了这种 Coatsome-复制子载体在小鼠中诱导 RepRNA 介导的 CD8 T 细胞反应的功效。此外,我们对 RepRNA 的物理性质提供了新的见解,表明去除所有 CSFV 结构蛋白基因对 GOI 的翻译有积极影响。最后,我们成功地设计了编码猪繁殖与呼吸综合征病毒(PRRSV)抗原的 RepRNA 构建体,为具有潜在应用价值的抗原表达提供了一个范例,可用于对抗病毒疾病。这些 Coatsome-复制子载体配方的可修改性和制造的简单性是应对可预见的新出现的大流行的主要优势。