Evidence map›Paper›PMID 41126351›Full record

ReviewMilitary Medical Research2025

Emerging strategies for monkeypox: antigen and antibody applications in diagnostics, vaccines, and treatments.

Wei Wang, Jia-Xiu Li, Si-Qi Long, Zi-Ning Liu, Xi-Peng Li, Zhi-Hang Peng, Ju-Dun Zheng, Yu-Hui Liao

Abstract readReview
In one paragraph

Review in Military Medical Research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 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

8 authors.

Wei Wang *Institute for Engineering Medicine, Kunming Medical University, Kunming, 650500, China.
Jia-Xiu Li *Key Laboratory of Infectious Diseases Research in South China, Ministry of Education, Southern Medical University, Guangzhou, 510091, China.
Si-Qi Long *Key Laboratory of Infectious Diseases Research in South China, Ministry of Education, Southern Medical University, Guangzhou, 510091, China.
Zi-Ning Liu *Key Laboratory of Infectious Diseases Research in South China, Ministry of Education, Southern Medical University, Guangzhou, 510091, China.
Xi-Peng LiInstitute for Engineering Medicine, Kunming Medical University, Kunming, 650500, China. lixipeng@kmmu.edu.cn.
Zhi-Hang PengNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, Chinese Center for Disease Control and Prevention, Beijing, 102206, China. pengzh@chinacdc.cn.
Ju-Dun ZhengInstitute for Engineering Medicine, Kunming Medical University, Kunming, 650500, China. zhengjd@i.smu.edu.cn.
Yu-Hui LiaoInstitute for Engineering Medicine, Kunming Medical University, Kunming, 650500, China. liaoyh8@mail.sysu.edu.cn.ORCID 0000-0003-4702-9516

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monkeypox, a zoonotic illness caused by monkeypox virus (MPXV), has been declared a public health emergency of international concern by the World Health Organization (WHO) on 2 separate occasions. The rapid spread and widespread transmission are closely associated with various proteins involved in the MPXV lifecycle, particularly surface antigen proteins found in mature virion (MV) and enveloped virion (EV), such as A29L, M1R, B6R, and A35R. These antigens are highly conserved in monkeypox virus (MPXV) and vaccinia virus (VACV), possessing cross-protective capabilities that can trigger broad immune protection against multiple orthopoxviruses, including MPXV. Vaccines based on DNA, mRNA, and recombinant proteins, targeting these antigens effectively address the current lack of specific monkeypox vaccines by triggering strong immune responses and ensuring the prevention of monkeypox. Compared to traditional vaccines, multi-epitope vaccines designed using computational tools such as reverse vaccinology and immunoinformatics offer lower development costs and faster validation processes. These multi-epitope vaccines also provide adaptability to mutations in MPXV strains. Additionally, these antigens and corresponding antibodies are useful for diagnosis and therapeutic monitoring, supporting early detection and offering novel treatments for cases resistant to existing antiviral drugs. This review provides a brief summary of recent progress and emerging trends in monkeypox detection, vaccine development, and antibody-based therapy targeting these antigens, offering new insights for monkeypox prevention and control.

Indexed as

Mpox, MonkeypoxAnimalsHumansMonkeypox virusVaccinia virusAntibodiesAntigensDetectionEnveloped virion (EV)Mature virion (MV)MonkeypoxMonkeypox virus (MPXV)Monoclonal antibodiesTherapyVaccines

Identifiers

PMID41126351
PMCPMC12548294

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.