Voellmy Richard, Bloom David C, Vilaboa Nuria
HSF Pharmaceuticals SA, 1814 La Tour-de-Peilz, Switzerland.
Department of Molecular Genetics and Microbiology, University of Florida College of Medicine, Gainesville, FL 32610-0266, USA.
Vaccines (Basel). 2020 May 18;8(2):230. doi: 10.3390/vaccines8020230.
Over the last few years, we have been evaluating a novel paradigm for immunization using viruses or virus-based vectors. Safety is provided not by attenuation or inactivation of vaccine viruses, but by the introduction into the viral genomes of genetic mechanisms that allow for stringent, deliberate spatial and temporal control of virus replication. The resulting replication-competent controlled viruses (RCCVs) can be activated to undergo one or, if desired, several rounds of efficient replication at the inoculation site, but are nonreplicating in the absence of activation. Extrapolating from observations that attenuated replicating viruses are better immunogens than replication-defective or inactivated viruses, it was hypothesized that RCCVs that replicate with wild-type-like efficiency when activated will be even better immunogens. The vigorous replication of the RCCVs should also render heterologous antigens expressed from them highly immunogenic. RCCVs for administration to skin sites or mucosal membranes were constructed using a virulent wild-type HSV-1 strain as the backbone. The recombinants are activated by a localized heat treatment to the inoculation site in the presence of a small-molecule regulator (SMR). Derivatives expressing influenza virus antigens were also prepared. Immunization/challenge experiments in mouse models revealed that the activated RCCVs induced far better protective immune responses against themselves as well as against the heterologous antigens they express than unactivated RCCVs or a replication-defective HSV-1 strain. Neutralizing antibody and proliferation responses mirrored these findings. We believe that the data obtained so far warrant further research to explore the possibility of developing effective RCCV-based vaccines directed to herpetic diseases and/or diseases caused by other pathogens.
在过去几年中,我们一直在评估一种使用病毒或基于病毒的载体进行免疫接种的新范式。安全性并非通过疫苗病毒的减毒或灭活来提供,而是通过将遗传机制引入病毒基因组来实现,这些遗传机制允许对病毒复制进行严格、有意的时空控制。由此产生的具有复制能力的可控病毒(RCCV)可以被激活,在接种部位进行一轮或(如果需要)几轮高效复制,但在没有激活的情况下不会复制。从减毒复制病毒比复制缺陷或灭活病毒是更好的免疫原这一观察结果推断,有人假设激活后以野生型样效率复制的RCCV将是更好的免疫原。RCCV的旺盛复制也应使其表达的异源抗原具有高度免疫原性。使用强毒野生型HSV-1毒株作为主干构建用于皮肤部位或粘膜给药的RCCV。重组体在小分子调节剂(SMR)存在下通过对接种部位进行局部热处理而被激活。还制备了表达流感病毒抗原的衍生物。小鼠模型中的免疫接种/攻毒实验表明,与未激活的RCCV或复制缺陷的HSV-1毒株相比,激活的RCCV对其自身以及它们表达的异源抗原诱导出更好的保护性免疫反应。中和抗体和增殖反应反映了这些发现。我们认为,迄今为止获得的数据值得进一步研究,以探索开发针对疱疹性疾病和/或由其他病原体引起的疾病的基于RCCV的有效疫苗的可能性。