Author
Listed:
- Lin Zhu
(Chinese Academy of Medical Sciences and Peking Union Medical College)
- Shuyuan Pan
(Beijing Institute of Biological Products Company Limited)
- Baoying Huang
(Chinese Center for Disease Control and Prevention)
- Junjie Zhang
(Chinese Center for Disease Control and Prevention)
- Zhaona Yang
(Beijing Institute of Biological Products Company Limited)
- Zhe Cong
(Chinese Academy of Medical Sciences and Peking Union Medical College)
- Jianrong Ma
(Chinese Academy of Medical Sciences and Peking Union Medical College)
- Shaoting Qiu
(Beijing Institute of Biological Products Company Limited)
- Yang Liu
(Beijing Institute of Biological Products Company Limited)
- Jingjing Zhang
(Chinese Academy of Medical Sciences and Peking Union Medical College)
- Na Li
(Chinese Academy of Medical Sciences and Peking Union Medical College)
- Jiahan Lu
(Chinese Academy of Medical Sciences and Peking Union Medical College)
- Ting Chen
(Chinese Academy of Medical Sciences and Peking Union Medical College)
- Yongzhi Hou
(Chinese Academy of Medical Sciences and Peking Union Medical College)
- Dong Zhang
(Chinese Academy of Medical Sciences and Peking Union Medical College)
- Qiang Wei
(Chinese Academy of Medical Sciences and Peking Union Medical College)
- Dan Li
(Chinese Center for Disease Control and Prevention)
- Wenjie Tan
(Chinese Center for Disease Control and Prevention)
- Yuntao Zhang
(Beijing Institute of Biological Products Company Limited)
- Jing Xue
(Chinese Academy of Medical Sciences and Peking Union Medical College)
Abstract
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.
Suggested Citation
Lin Zhu & Shuyuan Pan & Baoying Huang & Junjie Zhang & Zhaona Yang & Zhe Cong & Jianrong Ma & Shaoting Qiu & Yang Liu & Jingjing Zhang & Na Li & Jiahan Lu & Ting Chen & Yongzhi Hou & Dong Zhang & Qian, 2025.
"Tiantan vaccinia virus-based vaccine with promising safety provides sustained protection against mpox in non-human primates,"
Nature Communications, Nature, vol. 16(1), pages 1-17, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62594-0
DOI: 10.1038/s41467-025-62594-0
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