Max von Pettenkofer Institute Virology, and Gene Center, LMU Munich, Munich, Germany.
Department of Veterinary Medicine, Paul-Ehrlich-Institute, Langen, Germany.
PLoS Pathog. 2021 Apr 21;17(4):e1009064. doi: 10.1371/journal.ppat.1009064. eCollection 2021 Apr.
Vaccines of outstanding efficiency, safety, and public acceptance are needed to halt the current SARS-CoV-2 pandemic. Concerns include potential side effects caused by the antigen itself and safety of viral DNA and RNA delivery vectors. The large SARS-CoV-2 spike (S) protein is the main target of current COVID-19 vaccine candidates but can induce non-neutralizing antibodies, which might cause vaccination-induced complications or enhancement of COVID-19 disease. Besides, encoding of a functional S in replication-competent virus vector vaccines may result in the emergence of viruses with altered or expanded tropism. Here, we have developed a safe single round rhabdovirus replicon vaccine platform for enhanced presentation of the S receptor-binding domain (RBD). Structure-guided design was employed to build a chimeric minispike comprising the globular RBD linked to a transmembrane stem-anchor sequence derived from rabies virus (RABV) glycoprotein (G). Vesicular stomatitis virus (VSV) and RABV replicons encoding the minispike not only allowed expression of the antigen at the cell surface but also incorporation into the envelope of secreted non-infectious particles, thus combining classic vector-driven antigen expression and particulate virus-like particle (VLP) presentation. A single dose of a prototype replicon vaccine complemented with VSV G, VSVΔG-minispike-eGFP (G), stimulated high titers of SARS-CoV-2 neutralizing antibodies in mice, equivalent to those found in COVID-19 patients, and protected transgenic K18-hACE2 mice from COVID-19-like disease. Homologous boost immunization further enhanced virus neutralizing activity. The results demonstrate that non-spreading rhabdovirus RNA replicons expressing minispike proteins represent effective and safe alternatives to vaccination approaches using replication-competent viruses and/or the entire S antigen.
需要具有出色的效率、安全性和公众接受度的疫苗来阻止当前的 SARS-CoV-2 大流行。人们关注的问题包括抗原本身引起的潜在副作用以及病毒 DNA 和 RNA 递送载体的安全性。大型 SARS-CoV-2 刺突(S)蛋白是当前 COVID-19 疫苗候选物的主要靶标,但可以诱导非中和抗体,这可能导致接种后并发症或 COVID-19 疾病加重。此外,复制型病毒载体疫苗中 S 蛋白的功能编码可能导致具有改变或扩展嗜性的病毒出现。在这里,我们开发了一种安全的单次轮状病毒复制子疫苗平台,用于增强 S 受体结合域(RBD)的呈现。采用结构指导设计构建了一种嵌合的微小刺突,该刺突由与源自狂犬病病毒(RABV)糖蛋白(G)的跨膜茎锚序列连接的球形 RBD 组成。编码微小刺突的水疱性口炎病毒(VSV)和 RABV 复制子不仅允许抗原在细胞表面表达,而且还可以整合到分泌的非感染性颗粒的包膜中,从而将经典的载体驱动的抗原表达与颗粒病毒样颗粒(VLP)呈现相结合。与 VSV G 互补的原型复制子疫苗的单一剂量,刺激了小鼠体内 SARS-CoV-2 中和抗体的高滴度,相当于 COVID-19 患者中的滴度,并保护转基因 K18-hACE2 小鼠免受 COVID-19 样疾病的侵害。同源增强免疫进一步增强了病毒中和活性。结果表明,表达微小刺突蛋白的非传播性 Rhabdovirus RNA 复制子是使用复制型病毒和/或整个 S 抗原进行疫苗接种的有效且安全的替代方法。