病毒学
免疫原
免疫原性
异源的
生物
狂犬病
狂犬病病毒
重组DNA
免疫系统
鸭胚疫苗
中和
狂犬病疫苗
登革热疫苗
病毒
抗体
免疫学
登革热病毒
遗传学
基因
单克隆抗体
作者
Jingbo Huang,Weiqi Wang,Hailun Li,Yujie Bai,Yumeng Song,Cuicui Jiao,Hongli Jin,Pei Huang,Haili Zhang,Xianzhu Xia,Feihu Yan,Yuanyuan Li,Hualei Wang
标识
DOI:10.1016/j.antiviral.2024.105905
摘要
The rapid emergence of Severe Acute Respiratory Syndrome Coronavirus type 2 (SARS-CoV-2) variants, coupled with severe immune evasion and imprinting, has jeopardized the vaccine efficacy, necessitating urgent development of broad protective vaccines. Here, we propose a strategy employing recombinant rabies viruses (RABV) to create a universal SARS-CoV-2 vaccine expressing heterologous tandem receptor-binding domain (RBD) trimer from the SARS-CoV-2 Prototype, Delta, and Omicron strains (SRV-PDO). The results of mouse immunization indicated that SRV-PDO effectively induced cellular and humoral immune responses, and demonstrated higher immunogenicity and broader SARS-CoV-2 neutralization compared to the recombinant RABVs that only expressed RBD monomers. Moreover, SRV-PDO exhibited full protection against SARS-CoV-2 in the challenge assay. This study demonstrates that recombinant RABV expressing tandem RBD-heterotrimer as a multivalent immunogen could elicit a broad-spectrum immune response and potent protection against SARS-CoV-2, making it a promising candidate for future human or veterinary vaccines and offering a novel perspective in other vaccine design.
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