Evidence map›Paper›PMID 32581148›Full record

ArticleThe Journal of veterinary medical science2020

Recombinant vesicular stomatitis virus glycoprotein carrying a foot-and-mouth disease virus epitope as a vaccine candidate.

Hyang-Sim Lee, Sun-Young Park, Ah-Young Kim, Sang-Oh Lee, Jae-Seok Kim, Hyejin Kim, Hee-Jeong Youn, Young-Joon Ko

Open access · diamondAbstract read
In one paragraph

Article in The Journal of veterinary medical science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Molecular characterization ofVeterinary world · 2024
    Article
  4. Review
  5. Article
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 at 4 institutions in 2 countries.

Hyang-Sim LeeAnimal and Plant Quarantine Agency, Gimcheon, Gyeonsangbuk-do 39660, Republic of Korea.
Sun-Young ParkAnimal and Plant Quarantine Agency, Gimcheon, Gyeonsangbuk-do 39660, Republic of Korea.
Ah-Young KimAnimal and Plant Quarantine Agency, Gimcheon, Gyeonsangbuk-do 39660, Republic of Korea.
Sang-Oh LeeRespectBio Co., Ltd., Seoul, 04799, Republic of Korea.
Jae-Seok KimAnimal and Plant Quarantine Agency, Gimcheon, Gyeonsangbuk-do 39660, Republic of Korea.
Hyejin KimAnimal and Plant Quarantine Agency, Gimcheon, Gyeonsangbuk-do 39660, Republic of Korea.
Hee-Jeong YounCollege of Veterinary Medicine, Seoul National University, Seoul, 08826, Republic of Korea.
Young-Joon KoAnimal and Plant Quarantine Agency, Gimcheon, Gyeonsangbuk-do 39660, Republic of Korea.
Animal and Plant Quarantine Agency · KRNew Generation University College · ETRBio (South Korea) · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Foot-and-mouth disease (FMD) is one of the most highly contagious animal diseases. In an effort to overcome the drawbacks of the currently used inactivated foot-and-mouth disease virus vaccine, a novel recombinant protein carrying foot-and-mouth disease virus VP1 GH loop epitope linked to vesicular stomatitis virus glycoprotein was expressed in a baculovirus system. Its antigenicity was confirmed with ELISA using monoclonal antibody against foot-and-mouth disease virus. Twice immunizations one month apart in field pigs resulted in a significant antibody increase compared to the glutathione S-transferase carrier containing the same epitope and the commercial vaccine. To my knowledge, this is the first report that the recombinant protein vaccine was superior to the current vaccine. Although further studies are required to examine their immunogenicity in a large number of animals, this study sheds light on the development of a novel recombinant protein vaccine that could be easily produced in a general laboratory as an alternative to the current FMD vaccine, which requires a biosafety level 3 containment facility for vaccine production.

Indexed as

AnimalsBaculoviridaeEnzyme-Linked Immunosorbent AssayEpitopesFoot-and-Mouth DiseaseFoot-and-Mouth Disease VirusGlycoproteinsImmunizationRecombinant ProteinsSwineSwine DiseasesVaccines, SyntheticVesicular stomatitis New Jersey virusViral VaccinesEpitopesGlycoproteinsRecombinant ProteinsVaccines, SyntheticViral Vaccinesepitopefoot-and-mouth vaccineglycoproteinvesicular stomatitis virus

Identifiers

PMID32581148
PMCPMC7468052
OpenAlexW3036203944

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.