Evidence map›Paper›PMID 33952643›Full record

ArticleJournal of virology2021

A Cell Culture-Adapted Vaccine Virus against the Current African Swine Fever Virus Pandemic Strain.

M V Borca, A Rai, E Ramirez-Medina, E Silva, L Velazquez-Salinas, E Vuono, S Pruitt, N Espinoza, D P Gladue

Open access · greenAbstract readClinical Trial, Veterinary
In one paragraph

Article in Journal of virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
18.4field-weighted citation impact, top 1% 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

70 citing papers in PubMed, 98 citations in OpenAlex.

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10 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 1 country.

M V BorcaPlum Island Animal Disease Center, ARS, USDA, Greenport, New York, USA.
A RaiPlum Island Animal Disease Center, ARS, USDA, Greenport, New York, USA.
E Ramirez-MedinaPlum Island Animal Disease Center, ARS, USDA, Greenport, New York, USA.
E SilvaPlum Island Animal Disease Center, ARS, USDA, Greenport, New York, USA.
L Velazquez-SalinasPlum Island Animal Disease Center, ARS, USDA, Greenport, New York, USA.
E VuonoPlum Island Animal Disease Center, ARS, USDA, Greenport, New York, USA.
S PruittPlum Island Animal Disease Center, ARS, USDA, Greenport, New York, USA.
N EspinozaPlum Island Animal Disease Center, ARS, USDA, Greenport, New York, USA.
D P GladuePlum Island Animal Disease Center, ARS, USDA, Greenport, New York, USA.
Plum Island Animal Disease Center · USKansas State University · USOak Ridge Associated Universities · USUniversity of Connecticut · US

Funding

U.S. Department of Homeland Security (DHS) 70RSAT19KPM000138
6 · The paper itself

Abstract

African swine fever virus (ASFV) causes a virulent, deadly infection in wild and domestic swine and is currently causing a pandemic covering a contiguous geographical area from Central and Eastern Europe to Asia. No commercial vaccines are available to prevent African swine fever (ASF), resulting in devastating economic losses to the swine industry. The most advanced vaccine candidates are live attenuated strains developed using a genetically modified virulent parental virus. Recently, we developed a vaccine candidate, ASFV-G-ΔI177L, by deleting the I177L gene from the genome of the highly virulent ASFV pandemic strain Georgia (ASFV-G). ASFV-G-ΔI177L is safe and highly efficacious in challenge studies using parental ASFV-G. Large-scale production of ASFV-G-ΔI177L has been limited because it can replicate efficiently only in primary swine macrophages. Here, we present the development of an ASFV-G-ΔI177L derivative strain, ASFV-G-ΔI177L/ΔLVR, that replicates efficiently in a stable porcine cell line. In challenge studies, ASFV-G-ΔI177L/ΔLVR maintained the same level of attenuation, immunogenic characteristics, and protective efficacy as ASFV-G-ΔI177L. ASFV-G-ΔI177L/ΔLVR is the first rationally designed ASF vaccine candidate that can be used for large-scale commercial vaccine manufacture.

Indexed as

African Swine FeverAfrican Swine Fever VirusAnimalsCell Culture TechniquesCell LineImmunogenicity, VaccineMacrophagesPandemicsSequence DeletionSwineVaccines, AttenuatedViral VaccinesVirus CultivationVirus ReplicationVaccines, AttenuatedViral VaccinesAfrican swine feverAfrican swine fever virusASFASFVvaccine

Identifiers

PMID33952643
PMCPMC8315737
OpenAlexW3159288315

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.