Wichgers Schreur Paul J, Mooij Petra, Koopman Gerrit, Verstrepen Babs E, Fagrouch Zahra, Mortier Daniella, van Driel Nikki, Kant Jet, van de Water Sandra, Bogers Willy M, Punt Carine, van Keulen Lucien, Verschoor Ernst J, Kortekaas Jeroen
Department of Virology and Molecular Biology, Wageningen Bioveterinary Research, Wageningen University & Research, Lelystad, The Netherlands.
BunyaVax B.V., Lelystad, The Netherlands.
NPJ Vaccines. 2022 May 18;7(1):54. doi: 10.1038/s41541-022-00476-y.
Rift Valley fever virus (RVFV) is an emerging mosquito-borne bunyavirus that is highly pathogenic to wild and domesticated ruminants, camelids, and humans. While animals are exclusively infected via mosquito bites, humans can also be infected via contact with contaminated tissues or blood. No human vaccine is available and commercialized veterinary vaccines do not optimally combine efficacy with safety. We previously reported the development of two novel live-attenuated RVF vaccines, created by splitting the M genome segment and deleting the major virulence determinant NSs. The vaccine candidates, referred to as the veterinary vaccine vRVFV-4s and the human vaccine hRVFV-4s, were shown to induce protective immunity in multiple species after a single vaccination. Anticipating accidental exposure of humans to the veterinary vaccine and the application of hRVFV-4s to humans, the safety of each vaccine was evaluated in the most susceptible nonhuman primate model, the common marmoset (Callithrix jacchus). Marmosets were inoculated with high doses of each vaccine and were monitored for clinical signs as well as for vaccine virus dissemination, shedding, and spreading to the environment. To accurately assess the attenuation of both vaccine viruses, separate groups of marmosets were inoculated with the parent wild-type RVFV strains. Both wild-type strains induced high viremia and disseminated to primary target organs, associated with mild-to-severe morbidity. In contrast, both vaccines were well tolerated with no evidence of dissemination and shedding while inducing potent neutralizing antibody responses. The results of the studies support the unprecedented safety profile of both vaccines for animals and humans.
裂谷热病毒(RVFV)是一种新出现的蚊媒布尼亚病毒,对野生和家养反刍动物、骆驼科动物及人类具有高度致病性。动物仅通过蚊虫叮咬感染,而人类也可通过接触受污染的组织或血液感染。目前尚无人类疫苗,商业化的兽用疫苗也未在疗效与安全性方面达到最佳平衡。我们之前报道了两种新型减毒活RVF疫苗的研发,这两种疫苗是通过拆分M基因组片段并删除主要毒力决定因子NSs而制备的。这两种候选疫苗,即兽用疫苗vRVFV - 4s和人用疫苗hRVFV - 4s,在单次接种后能在多个物种中诱导产生保护性免疫。鉴于预计人类会意外接触兽用疫苗以及hRVFV - 4s会应用于人类,我们在最易感的非人灵长类动物模型普通狨猴(Callithrix jacchus)中评估了每种疫苗的安全性。给狨猴接种高剂量的每种疫苗,并监测其临床症状以及疫苗病毒的传播、排泄和向环境中的扩散情况。为准确评估两种疫苗病毒的减毒情况,将单独的狨猴组接种亲本野生型RVFV毒株。两种野生型毒株均诱导了高病毒血症,并扩散至主要靶器官,伴有轻度至重度发病。相比之下,两种疫苗均耐受性良好,没有传播和排泄的迹象,同时诱导了强效的中和抗体反应。这些研究结果支持了这两种疫苗对动物和人类前所未有的安全性。