Jiahao Wu, Wei Rou, Zhengrong Gao, Xu Ma, Haoyi Ding, Tingting Zheng, Lei Wang, Lu Zhao, Kai Yang, Xiaoyu Li, Yongfeng Qiao, Shihua Li, Xiao Qu, Chunbo Dong, Guocan Yu, Jikui Deng, Han Wang, Hangping Yao, Haidong Wang, George Fu Gao, Zhida Liu
{"title":"CircRNA vaccine encoding a chimeric immunogen of B6 and M1 demonstrates robust immune responses against MPXV.","authors":"Jiahao Wu, Wei Rou, Zhengrong Gao, Xu Ma, Haoyi Ding, Tingting Zheng, Lei Wang, Lu Zhao, Kai Yang, Xiaoyu Li, Yongfeng Qiao, Shihua Li, Xiao Qu, Chunbo Dong, Guocan Yu, Jikui Deng, Han Wang, Hangping Yao, Haidong Wang, George Fu Gao, Zhida Liu","doi":"10.1016/j.celrep.2025.116432","DOIUrl":null,"url":null,"abstract":"<p><p>The mpox outbreak has been declared a Public Health Emergency of International Concern on two occasions, with the status remaining effective, highlighting the urgency of this global health crisis. Developing safe and effective vaccines specifically targeting the MPXV is therefore critical. Our current study presents a bivalent circular RNA (circRNA) vaccine encoding a chimeric immunogen comprising the tandem fusion of MPXV extracellular enveloped virions antigen B6 and intracellular mature virions antigen M1 (CircRNA<sup>B6M1</sup>). The B6M1 chimeric immunogen preserves the conformation of the major neutralizing epitopes derived from both antigens. Furthermore, the CircRNA<sup>B6M1</sup> vaccine elicits potent neutralizing antibodies against both MPXV and VACV, while also inducing antigen-specific T cell responses. Notably, the CircRNA<sup>B6M1</sup> vaccine confers complete protection to immunized mice against the lethal VACV challenge. Collectively, these findings identify promising immunogen candidates for developing next-generation circRNA vaccines against the MPXV and other orthopoxviruses.</p>","PeriodicalId":9798,"journal":{"name":"Cell reports","volume":"44 10","pages":"116432"},"PeriodicalIF":6.9000,"publicationDate":"2025-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell reports","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.celrep.2025.116432","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The mpox outbreak has been declared a Public Health Emergency of International Concern on two occasions, with the status remaining effective, highlighting the urgency of this global health crisis. Developing safe and effective vaccines specifically targeting the MPXV is therefore critical. Our current study presents a bivalent circular RNA (circRNA) vaccine encoding a chimeric immunogen comprising the tandem fusion of MPXV extracellular enveloped virions antigen B6 and intracellular mature virions antigen M1 (CircRNAB6M1). The B6M1 chimeric immunogen preserves the conformation of the major neutralizing epitopes derived from both antigens. Furthermore, the CircRNAB6M1 vaccine elicits potent neutralizing antibodies against both MPXV and VACV, while also inducing antigen-specific T cell responses. Notably, the CircRNAB6M1 vaccine confers complete protection to immunized mice against the lethal VACV challenge. Collectively, these findings identify promising immunogen candidates for developing next-generation circRNA vaccines against the MPXV and other orthopoxviruses.
期刊介绍:
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