Institut für Virologie und Immunologie (IVI), Sensemattstrasse 293, CH-3147 Mittelhäusern, Switzerland.
Bavarian Nordic GmbH, Fraunhoferstraße 13, D-82152 Martinsried, Germany.
J Gen Virol. 2018 Jul;99(7):866-879. doi: 10.1099/jgv.0.001085. Epub 2018 Jun 5.
Vesicular stomatitis virus (VSV) expressing the Ebola virus (EBOV) glycoprotein (GP) in place of the VSV glycoprotein G (VSV/EBOV-GP) is a promising EBOV vaccine candidate which has already entered clinical phase 3 studies. Although this chimeric virus was tolerated overall by volunteers, it still caused viremia and adverse effects such as fever and arthritis, suggesting that it might not be sufficiently attenuated. In this study, the VSV/EBOV-GP vector was further modified in order to achieve attenuation while maintaining immunogenicity. All recombinant VSV constructs were propagated on VSV G protein expressing helper cells and used to immunize guinea pigs via the intramuscular route. The humoral immune response was analysed by EBOV-GP-specific fluorescence-linked immunosorbent assay, plaque reduction neutralization test and in vitro virus-spreading inhibition test that employed recombinant VSV/EBOV-GP expressing either green fluorescent protein or secreted Nano luciferase. Most modified vector constructs induced lower levels of protective antibodies than the parental VSV/EBOV-GP or a recombinant modified vaccinia virus Ankara vector encoding full-length EBOV-GP. However, the VSV/EBOV-GP(F88A) mutant was at least as immunogenic as the parental vaccine virus although it was highly propagation-restricted. This finding suggests that VSV-vectored vaccines need not be propagation-competent to induce a robust humoral immune response. However, VSV/EBOV-GP(F88A) rapidly reverted to a fully propagation-competent virus indicating that a single-point mutation is not sufficient to maintain the propagation-restricted phenotype.
水疱性口炎病毒(VSV)表达埃博拉病毒(EBOV)糖蛋白(GP)取代 VSV 糖蛋白 G(VSV/EBOV-GP)是一种有前途的 EBOV 疫苗候选物,已进入临床 3 期研究。尽管这种嵌合病毒总体上被志愿者耐受,但它仍引起病毒血症和发热、关节炎等不良反应,表明它可能没有足够减毒。在这项研究中,进一步修饰了 VSV/EBOV-GP 载体,以在保持免疫原性的同时实现减毒。所有重组 VSV 构建体均在表达 VSV G 蛋白的辅助细胞上繁殖,并通过肌肉内途径用于免疫豚鼠。通过埃博拉病毒 GP 特异性荧光酶联免疫吸附试验、蚀斑减少中和试验和体外病毒扩散抑制试验分析体液免疫反应,该试验使用表达绿色荧光蛋白或分泌纳米荧光素酶的重组 VSV/EBOV-GP。大多数修饰的载体构建体诱导的保护性抗体水平低于亲本 VSV/EBOV-GP 或编码全长 EBOV-GP 的重组改良痘苗病毒 Ankara 载体。然而,尽管 VSV/EBOV-GP(F88A) 突变体的增殖受到严重限制,但它的免疫原性至少与亲本疫苗病毒一样。这一发现表明,VSV 载体疫苗不需要具有增殖能力就能诱导强大的体液免疫反应。然而,VSV/EBOV-GP(F88A) 迅速恢复为完全增殖能力的病毒,表明单点突变不足以维持增殖受限表型。