Evidence map›Paper›PMID 41665626›Full record

ArticleEmerging microbes & infections2026

Potent neutralization of Rift Valley fever virus mediated by monoclonal antibodies via concurrent inhibition of attachment and fusion.

Meng Hao, Ting Bian, Zhengshan Chen, Guanying Zhang, Chuanyi Zhao, Guangcheng Fu, Yi Chen, Xiangyang Chi, Pengfei Fan, Ting Fang and 2 more

Abstract read
In one paragraph

Article in Emerging microbes & infections, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

12 authors.

Meng HaoLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Ting BianLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Zhengshan ChenLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Guanying ZhangLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Chuanyi ZhaoLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Guangcheng FuLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Yi ChenLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Xiangyang ChiLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Pengfei FanLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Ting FangLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Changming YuLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.
Jianmin LiLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rift Valley fever virus (RVFV) is one of the most important mosquito-borne pathogens that causes substantial morbidity and mortality in livestock and humans. Despite its public health and economic impact, no licenced vaccines or therapeutics are currently available for human use. Here, we report the isolation of a panel of Gn-specific monoclonal antibodies (mAbs) from the memory B cells of rhesus macaques immunized with Ad4-GnGc or Ad5-GnGc. 20 mAbs with neutralizing activity were identified and divided into two groups, targeting subdomain I and subdomain III of the Gn protein, respectively. In murine infection models, representative nAbs A38 and A13 demonstrated efficacious protection against RVFV infection in both prophylactic and therapeutic settings. Research on the neutralizing mechanisms of antibodies revealed that A13 mainly mediates neutralization by inhibiting RVFV fusion to cells, while A38 disrupts multiple stages of the viral entry process by blocking both virus attachment and membrane fusion. To gain deeper insights into these mechanisms, we predicted the variable regions of antibodies and performed molecular docking with RVFV Gn head domain. Structural analysis showed that A38 binds to the DI and DIII subdomains, while A13 binds to an epitope spanning three subdomains of Gn, likely preventing the structural rearrangements required for membrane fusion. This study identifies multiple promising therapeutic candidates against RVFV and elucidates the structural mechanisms by which neutralizing antibodies inhibit various stages of the viral life cycle. These findings deepen our understanding of RVFV pathogenesis and will facilitate the development of novel therapeutic strategies.

Indexed as

Antibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralRift Valley FeverRift Valley fever virusVirus AttachmentVirus InternalizationAnimalsFemaleHumansMacaca mulattaMiceMice, Inbred BALB CMolecular Docking SimulationAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, Viralantiviral mechanismattachment and fusion inhibitionGn proteinneutralizing antibodiesRVFV

Identifiers

PMID41665626
PMCPMC12893178

What Socratic 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 Socratic graph.