Zhu Lin, Pan Shuyuan, Huang Baoying, Zhang Junjie, Yang Zhaona, Cong Zhe, Ma Jianrong, Qiu Shaoting, Liu Yang, Zhang Jingjing, Li Na, Lu Jiahan, Chen Ting, Hou Yongzhi, Zhang Dong, Wei Qiang, Li Dan, Tan Wenjie, Zhang Yuntao, Xue Jing
State Key Laboratory of Respiratory Health and Multimorbidity, NHC Key Laboratory of Human Disease Comparative Medicine, Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Beijing Institute of Biological Products Company Limited, Beijing, China.
Nat Commun. 2025 Aug 5;16(1):7183. doi: 10.1038/s41467-025-62594-0.
The World Health Organization (WHO) has declared the mpox outbreak a public health emergency of international concern (PHEIC). Safe and efficient vaccines against the mpox virus (MPXV) are urgently needed to impede the surge in cases. Here, we report the results of a preclinical study employing different dosing strategies on a vaccine candidate named NTV, obtained via targeted gene deletion in the Tiantan strain vaccinia virus, resulting in a replication-deficient variant. Following optimisation of the NTV immunization dose and confirmation of its protective efficacy against MPXV in a mouse model, we demonstrate that a two-shot NTV regimen in macaques elicits significant neutralizing antibody and cellular immune responses, providing efficient protection against MPXV challenge. Notably, we find that a single NTV dose or long-term immunization in macaques offer effective protection against moderate or severe mpox disease by enhancing cellular immunity and rapidly evoking neutralizing antibodies. These results demonstrate the vaccine's potential for emergency use and for long-lasting protection. Safety evaluations show no adverse effects in macaques receiving triple the standard dosage in three consecutive injections. These findings highlight the potential of the NTV vaccine candidate with key advantages, including robust immunogenicity, sustained protective efficacy, and safety in preclinical settings.
世界卫生组织(WHO)已宣布猴痘疫情为国际关注的突发公共卫生事件(PHEIC)。迫切需要安全有效的抗猴痘病毒(MPXV)疫苗来阻止病例激增。在此,我们报告了一项临床前研究的结果,该研究对一种名为NTV的候选疫苗采用了不同的给药策略,NTV是通过对天坛株痘苗病毒进行靶向基因缺失获得的,产生了一种复制缺陷型变体。在优化NTV免疫剂量并在小鼠模型中确认其对MPXV的保护效力后,我们证明在猕猴中采用两剂NTV方案可引发显著的中和抗体和细胞免疫反应,为抵御MPXV攻击提供有效保护。值得注意的是,我们发现猕猴单次接种NTV或长期免疫可通过增强细胞免疫和迅速产生中和抗体,为中度或重度猴痘疾病提供有效保护。这些结果证明了该疫苗的紧急使用潜力和持久保护能力。安全性评估显示,连续三次注射三倍标准剂量的猕猴未出现不良反应。这些发现突出了候选NTV疫苗的潜力,其具有关键优势,包括强大的免疫原性、持续的保护效力以及临床前环境中的安全性。