Evidence map›Paper›PMID 36439179›Full record

ArticleFrontiers in immunology2022

Single-dose of a replication-competent adenovirus-vectored vaccine provides sterilizing protection against Rift Valley fever virus challenge.

Ting Bian, Busen Wang, Guangcheng Fu, Meng Hao, Yi Chen, Ting Fang, Shuling Liu, Changming Yu, Jianmin Li, Wei Chen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Cryo-EM structure of the Rift Valley fever virus envelope protein in complex with a potent neutralization antibody.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

10 authors at 1 institution in 1 country.

Ting BianBeijing Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China.
Busen WangBeijing Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China.
Guangcheng FuBeijing Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China.
Meng HaoBeijing Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China.
Yi ChenBeijing Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China.
Ting FangBeijing Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China.
Shuling LiuBeijing Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China.
Changming YuBeijing Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China.
Jianmin LiBeijing Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China.
Wei ChenBeijing Institute of Biotechnology, Academy of Military Medical Sciences, Beijing, China.
Academy of Military Medical Sciences · CN

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 virulent pathogens causing severe disease in animals and humans. However, there is currently no approved vaccine to prevent RVFV infection in humans. The use of human adenovirus serotype 4 (Ad4) as a vector for an RVFV vaccine has not been reported. Here, we report the generation of a replication-competent recombinant Ad4 vector expressing codon-optimized forms of the RVFV glycoproteins Gn and Gc (named Ad4-GnGc). Intramuscular immunization with Ad4-GnGc elicited robust neutralizing antibodies against RVFV and cellular immune responses in mice. A single low-dose vaccination with Ad4-GnGc completely protected interferon-α/β receptor-deficient A129 mice from lethal RVFV infection. More importantly, Ad4-GnGc efficacy was not affected by pre-existing immunity to adenovirus serotype 5, which currently exists widely in populations. These results suggest that Ad4-GnGc is a promising vaccine candidate against RVFV.

Indexed as

Adenoviridae InfectionsAdenovirus VaccinesRift Valley FeverRift Valley fever virusViral VaccinesAdenoviridaeAnimalsHumansMiceAdenovirus VaccinesViral Vaccinesadenovirus serotype 4 vectorglycoproteinsreplication-competentRVFV vaccinesingle-dose immunizationsterilizing protection

Identifiers

PMID36439179
PMCPMC9691644
OpenAlexW4308936087

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.