Evidence map›Paper›PMID 35604219›Full record

ArticleJournal of virology2022

BacMam Expressing Highly Glycosylated Porcine Interferon Alpha Induces Robust Antiviral and Adjuvant Effects against Foot-and-Mouth Disease Virus in Pigs.

Aro Kim, Gyeongmin Lee, Ji-Hyeon Hwang, Jong-Hyeon Park, Min Ja Lee, Byounghan Kim, Su-Mi Kim

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. 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

7 authors at 1 institution in 1 country.

Aro KimCenter for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agencygrid.466502.3, Gimcheon City, Gyeongsangbuk-do, Republic of Korea.
Gyeongmin LeeCenter for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agencygrid.466502.3, Gimcheon City, Gyeongsangbuk-do, Republic of Korea.
Ji-Hyeon HwangCenter for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agencygrid.466502.3, Gimcheon City, Gyeongsangbuk-do, Republic of Korea.
Jong-Hyeon ParkCenter for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agencygrid.466502.3, Gimcheon City, Gyeongsangbuk-do, Republic of Korea.
Min Ja LeeCenter for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agencygrid.466502.3, Gimcheon City, Gyeongsangbuk-do, Republic of Korea.
Byounghan KimCenter for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agencygrid.466502.3, Gimcheon City, Gyeongsangbuk-do, Republic of Korea.
Su-Mi KimCenter for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agencygrid.466502.3, Gimcheon City, Gyeongsangbuk-do, Republic of Korea.ORCID 0000-0002-9242-2731
Animal and Plant Quarantine Agency · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Foot-and-mouth disease (FMD) is an acute contagious disease that affects cloven-hoofed animals and has severe global economic consequences. FMD is most commonly controlled by vaccination. Currently available commercial FMD vaccines contain chemically inactivated whole viruses, which are thought to be slow acting as they are effective only 4 to 7 days following vaccination. Hence, the development of a novel rapid vaccine or alternative measures, such as antiviral agents or the combination of vaccines and antiviral agents for prompt FMD virus (FMDV) outbreak containment, is desirable. Here, we constructed a recombinant baculovirus (BacMam) expressing consensus porcine interferon alpha (IFN-α) that has three additional N-glycosylation sites driven by a cytomegalovirus immediate early (CMV-IE) promoter (Bac-Con3N IFN-α) for protein expression in mammalian cells. Bac-Con3N IFN-α expressing highly glycosylated porcine IFN-α protein increased the duration of antiviral effects. We evaluated the antiviral effects of Bac-Con3N IFN-α in swine cells and mice and observed sustained antiviral effects in pig serum; additionally, Bac-Con3N IFN-α exhibited sustained antiviral effects

Indexed as

Foot-and-Mouth DiseaseFoot-and-Mouth Disease VirusInterferon-alphaViral VaccinesAdjuvants, ImmunologicAnimalsAntibodies, NeutralizingAntibodies, ViralAntiviral AgentsBaculoviridaeMiceSwineVaccines, InactivatedAdjuvants, ImmunologicAntibodies, NeutralizingAntibodies, ViralAntiviral AgentsInterferon-alphaVaccines, InactivatedViral VaccinesBacMamfoot-and-mouth disease virusinterferonsvaccines

Identifiers

PMID35604219
PMCPMC9215255
OpenAlexW4281296405

What OpenQuestion holds

Textmetadata
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.