Author
Listed:
- Qing Ye
(Academy of Military Medical Sciences)
- Dong Zhang
(Peking Union Medical College)
- Rong-Rong Zhang
(Academy of Military Medical Sciences)
- Qian Xu
(Wenzhou Medical University)
- Xing-Yao Huang
(Academy of Military Medical Sciences)
- Baoying Huang
(Chinese Center for Disease Control and Prevention)
- Meng-Xu Sun
(Academy of Military Medical Sciences)
- Zhe Cong
(Peking Union Medical College)
- Lin Zhu
(Peking Union Medical College)
- Jianrong Ma
(Peking Union Medical College)
- Na Li
(Peking Union Medical College)
- Jingjing Zhang
(Peking Union Medical College)
- Ting Chen
(Peking Union Medical College)
- Jiahan Lu
(Peking Union Medical College)
- Yongzhi Hou
(Peking Union Medical College)
- Xiang Chen
(Academy of Military Medical Sciences)
- Hai-Tao Liu
(Academy of Military Medical Sciences)
- Chao Zhou
(Academy of Military Medical Sciences)
- Rui-Ting Li
(Academy of Military Medical Sciences)
- Mei Wu
(Academy of Military Medical Sciences)
- Zheng-Jian Wang
(Academy of Military Medical Sciences)
- Jiye Yin
(Beijing Institute of Pharmacology and Toxicology)
- Ye-Feng Qiu
(Academy of Military Medical Science)
- Bo Ying
(Suzhou Abogen Biosciences Co., Ltd.)
- Wen-Jie Tan
(Chinese Center for Disease Control and Prevention)
- Jing Xue
(Peking Union Medical College)
- Cheng-Feng Qin
(Academy of Military Medical Sciences
Chinese Academy of Medical Sciences)
Abstract
The recent worldwide outbreaks of mpox prioritize the development of a safe and effective mRNA vaccine. The contemporary mpox virus (MPXV) exhibits changing virological and epidemiological features, notably affecting populations already vulnerable to human immunodeficiency virus (HIV). Herein, we profile the immunogenicity of AR-MPXV5, a penta-component mRNA vaccine targeting five specific proteins (M1R, E8L, A29L, A35R, and B6R) from the representative contemporary MPXV clade II strain, in both naive and simian immunodeficiency virus (SIV)-infected nonhuman primates. Immunization with two doses of AR-MPXV5 to cynomolgus macaques effectively elicits antibody responses and cellular responses. Importantly, based on the challenge model with a contemporary MPXV clade II strain, AR-MPXV5 demonstrates effective efficacy in preventing skin lesions, eliminating viremia and reducing viral loads in multiple tissues after challenge in naive male animals. More importantly, AR-MPXV5 is well-tolerated in stable chronic SIV-infected rhesus monkeys, while eliciting comparable MPXV-specific humoral and cellular responses in both naive and SIV-infected monkeys. Together, these results support further clinical development of the AR-MPXV5 vaccine.
Suggested Citation
Qing Ye & Dong Zhang & Rong-Rong Zhang & Qian Xu & Xing-Yao Huang & Baoying Huang & Meng-Xu Sun & Zhe Cong & Lin Zhu & Jianrong Ma & Na Li & Jingjing Zhang & Ting Chen & Jiahan Lu & Yongzhi Hou & Xian, 2024.
"A penta-component mpox mRNA vaccine induces protective immunity in nonhuman primates,"
Nature Communications, Nature, vol. 15(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54909-4
DOI: 10.1038/s41467-024-54909-4
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