Development and characterization of a plant-derived norovirus-like particle vaccine

免疫原性 病毒学 烟草 生物 类病毒颗粒 免疫系统 效价 抗体 抗原 病毒 抗体效价 微生物学 重组DNA 免疫学 生物化学 基因
作者
Janna R. Shapiro,Guadalupe Andreani,Charlotte Dubé,Mélanie Bérubé,Diane Bussière,Manon Couture,Michèle Dargis,Hilary E. Hendin,Nathalie Landry,Pierre‐Olivier Lavoie,Stéphane Pillet,Brian J. Ward,Marc‐André D’Aoust,Sonia Trépanier
出处
期刊:Vaccine [Elsevier]
卷期号:41 (41): 6008-6016 被引量:1
标识
DOI:10.1016/j.vaccine.2023.08.036
摘要

Norovirus (NoV) is the most common cause of diarrheal episodes globally. Issues with in vitro cultivation systems, genetic variation, and animal models have hindered vaccine development. Plant-derived virus-like particles (VLPs) may address some of these concerns because they are highly immunogenic, can be administered by different routes, and can be rapidly produced to accommodate emerging viral strains. NoV VLPs (NoVLP) composed of the surface viral protein (VP) 1 of the GI and GII genogroups were produced in Nicotiana benthamiana using an Agrobacterium tumefaciens-based recombinant transient expression system. Leaves from infiltrated plants were harvested and NoVLPs were extracted and purified. The safety and immunogenicity of the GII.4 NoVLP, the genotype currently causing most human disease, were subsequently examined in rabbits and mice. Fifteen GI and GII NoVLPs were successfully expressed in N. benthamiana and were structurally similar to NoV virions, as determined by cryogenic transmission electron microscopy. The NoVLP was well-tolerated, with no local or systemic signs of toxicity in rabbits. Three intramuscular doses of the GII.4 NoVLP adjuvanted with aluminum hydroxide induced robust IgG titers, IgG-secreting cells, histo-blood group antigen blocking titers, and IFNγ-secreting T cells in mice. In addition to circulating antibodies, oral administration of the NoVLP in mice induced significant IgA levels in feces, indicative of a mucosal response. The plant-made NoVLP vaccine was safe and immunogenic in mice and rabbits. Multi-modal vaccination, combining oral and intramuscular administration could be considered for future clinical development to maximize systemic and mucosal immune responses.
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