Evidence map›Paper›PMID 40140411›Full record

ArticleNature communications2025

An mRNA vaccine against monkeypox virus inhibits infection by co-activation of humoral and cellular immune responses.

Wanbo Tai, Chongyu Tian, Huicheng Shi, Benjie Chai, Xinyang Yu, Xinyu Zhuang, Pengyuan Dong, Min Li, Qi Yin, Shengyong Feng and 10 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Wanbo Tai *Institute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, China. taiwb@szbl.ac.cn.ORCID http://orcid.org/0000-0002-9864-8993
Chongyu Tian *Institute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, China.
Huicheng Shi *New Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, China.
Benjie Chai *New Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, China.
Xinyang Yu *Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, China.
Xinyu Zhuang *Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Pengyuan DongInstitute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, China.ORCID http://orcid.org/0009-0009-3922-2202
Min LiState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, China.
Qi YinState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, China.ORCID http://orcid.org/0009-0001-7614-7768
Shengyong FengNew Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, China.
Weixiao WangInstitute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, China.
Oujia ZhangNew Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, China.
Shibo LiangInstitute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, China.
Yang LiuInstitute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, China.
Jianying LiuInstitute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, China.
Longchao ZhuInstitute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, China.
Guangyu ZhaoState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, China. zhaoguangyu@bmi.ac.cn.ORCID http://orcid.org/0000-0002-0925-5216
Mingyao TianChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China. klwklw@126.com.ORCID http://orcid.org/0000-0003-0360-3635
Guocan YuKey Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, China. guocanyu@mail.tsinghua.edu.cn.ORCID http://orcid.org/0000-0003-1157-4184
Gong ChengNew Cornerstone Science Laboratory, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, China. gongcheng@mail.tsinghua.edu.cn.ORCID http://orcid.org/0000-0001-7447-5488

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32100755National Natural Science Foundation of China (National Science Foundation of China) 32188101National Natural Science Foundation of China (National Science Foundation of China) 32270182National Natural Science Foundation of China (National Science Foundation of China) 82241082National Natural Science Foundation of China (National Science Foundation of China) 82271872National Natural Science Foundation of China (National Science Foundation of China) 82341046National Natural Science Foundation of China (National Science Foundation of China) 82372254
6 · The paper itself

Abstract

The persistent monkeypox outbreaks intensify the demand for monkeypox vaccines. Based on the mRNA vaccine platform, we conduct a systematic screening of monkeypox virus (MPXV) surface proteins from two types of viral particles, extracellular enveloped viruses (EVs) and intracellular mature viruses (MVs). This screening unveils 12 important antigens with diverse levels of neutralizing immunogenicity. Further assessment reveals that the combinations of 4, 8, and 12 of these antigens, namely Mix-4, Mix-8, and Mix-12, induce varying degrees of immune protection, with Mix-12 being the most potent. This finding demonstrates the significance of not only the level but also the diversity of the neutralizing antibodies in providing potent immune protection. Additionally, we utilize a T cell-epitope enrichment strategy, analyzing the complete proteome sequence of the MPXV to predict antigenic epitope-rich regions. Integration of these epitope-rich regions into a cellular immune-targeting antigen, named MPX-EPs, showcases that a cellular immune-targeting mRNA vaccine can independently confer immune protection. Furthermore, co-immunization with Mix-12 and MPX-EPs achieves complete protection against MPXV challenge. Overall, these results suggest an effective approach to enhance the immune protection of mRNA vaccines through the specific coordination of humoral and cellular immune responses.

Indexed as

Immunity, CellularImmunity, HumoralMonkeypox virusMpox, MonkeypoxmRNA VaccinesViral VaccinesAnimalsAntibodies, NeutralizingAntibodies, ViralAntigens, ViralEpitopes, T-LymphocyteFemaleHumansMiceMice, Inbred BALB CVaccines, SyntheticAntibodies, NeutralizingAntibodies, ViralAntigens, ViralEpitopes, T-LymphocytemRNA VaccinesVaccines, SyntheticViral Vaccines

Identifiers

PMID40140411
PMCPMC11947304

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.