Department of Arbovirus Vaccines, National Institutes for Food and Drug Control, Beijing, China.
Vaccines R&D Department, Changchun Institute of Biological Products, Changchun, China.
Front Immunol. 2023 Oct 26;14:1288879. doi: 10.3389/fimmu.2023.1288879. eCollection 2023.
Rabies is a serious public health problem worldwide for which an effective treatment method is lacking but can be prevented by vaccines. Current vaccines are produced in cell or egg cultures, which are both costly and time consuming.
Here, a non-replicating mRNA vaccine (RV021) encoding the rabies virus glycoprotein was developed , and its immunogenicity and protective efficacy against live virus was evaluated in mice.
A two-dose vaccination with 1 μg of RV021 at 7-day intervals induced a protective level of neutralizing antibody that was maintained for at least 260 days. RV021 induced a robust cellular immune response that was significantly superior to that of an inactivated vaccine. Two doses of 1 μg RV021 provided full protection against challenge with CVS of 30~60-fold lethal dose, 50%. Vaccine potency testing (according to the National Institutes of Health) revealed that the potency of RV021 at 15 μg/dose was 7.5 IU/dose, which is substantially higher than the standard for lot release of rabies vaccines for current human use.
The mRNA vaccine RV021 induces a strong protective immune response in mice, providing a new and promising strategy for human rabies prevention and control.
狂犬病是全球范围内严重的公共卫生问题,目前尚无有效的治疗方法,但可通过疫苗预防。现有的狂犬病疫苗是在细胞或鸡蛋中培养生产的,既昂贵又耗时。
本研究构建了一种非复制型狂犬病病毒糖蛋白编码 mRNA 疫苗(RV021),并在小鼠中评价其免疫原性和对活病毒的保护效力。
间隔 7 天给予两剂 1μg RV021 可诱导产生保护水平的中和抗体,至少持续 260 天。RV021 诱导了强烈的细胞免疫反应,显著优于狂犬病灭活疫苗。两剂 1μg RV021 可提供针对 CVS 攻击的完全保护,效力为 30~60 倍致死剂量的 50%。疫苗效力检测(根据美国国立卫生研究院标准)显示,15μg/剂 RV021 的效力为 7.5IU/剂,显著高于当前人类使用狂犬病疫苗的批签发标准。
mRNA 疫苗 RV021 在小鼠中诱导了强烈的保护性免疫应答,为人类狂犬病预防和控制提供了一种新的有前途的策略。