Evidence map›Paper›PMID 26255831›Full record

ArticleMolecules and cells2015

Therapeutic Strategy for the Prevention of Pseudorabies Virus Infection in C57BL/6 Mice by 3D8 scFv with Intrinsic Nuclease Activity.

Gunsup Lee, SeungChan Cho, Phuong Mai Hoang, Dongjun Kim, Yongjun Lee, Eui-Joon Kil, Sung-June Byun, Taek-Kyun Lee, Dae-Hyun Kim, Sunghan Kim and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Molecules and cells, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  4. Review
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  9. Article
  10. ProbioticGenes · 2018
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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

11 authors at 3 institutions in 1 country.

Gunsup LeeDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Korea.
SeungChan ChoDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Korea.
Phuong Mai HoangDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Korea.
Dongjun KimDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Korea.
Yongjun LeeDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Korea.
Eui-Joon KilDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Korea.
Sung-June ByunAnimal Biotechnology Division, National Institute of Animal Science, Rural Development Administration, Suwon 441-706, Korea.
Taek-Kyun LeeSouth Sea Environment Research Department, Korea Institute of Ocean Science and Technology, Geoje 656-834, Korea.
Dae-Hyun KimFruit Research Division, National Institute of Horticultural and Herbal Science, Rural Development Administration, Suwon 440-706, Korea.
Sunghan KimDepartment of Plant Science, Research Institute of Agriculture and Life Sciences, and Plant Genomics and Breeding Institute, Seoul National University, Seoul 151-921, Korea.
Sukchan LeeDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Korea.
Sungkyunkwan University · KRRural Development Administration · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

3D8 single chain variable fragment (scFv) is a recombinant monoclonal antibody with nuclease activity that was originally isolated from autoimmune-prone MRL mice. In a previous study, we analyzed the nuclease activity of 3D8 scFv and determined that a HeLa cell line expressing 3D8 scFv conferred resistance to herpes simplex virus type 1 (HSV-1) and pseudorabies virus (PRV). In this study, we demonstrate that 3D8 scFv could be delivered to target tissues and cells where it exerted a therapeutic effect against PRV. PRV was inoculated via intramuscular injection, and 3D8 scFv was injected intraperitoneally. The observed therapeutic effect of 3D8 scFv against PRV was also supported by results from quantitative reverse transcription polymerase chain reaction, southern hybridization, and immunohistochemical assays. Intraperitoneal injection of 5 and 10 μg 3D8 scFv resulted in no detectable toxicity. The survival rate in C57BL/6 mice was 9% after intramuscular injection of 10 LD50 PRV. In contrast, the 3D8 scFv-injected C57BL/6 mice showed survival rates of 57% (5 μg) and 47% (10 μg). The results indicate that 3D8 scFv could be utilized as an effective antiviral agent in several animal models.

Indexed as

AnimalsAntibodies, MonoclonalAntiviral AgentsCell Line, TumorDeoxyribonucleasesDrug Evaluation, PreclinicalFemaleHerpesvirus 1, SuidMiceMice, Inbred C57BLPseudorabiesRatsRibonucleasesSingle-Chain AntibodiesTissue DistributionVirus ReplicationAntibodies, MonoclonalAntiviral AgentsDeoxyribonucleasesRibonucleasesSingle-Chain Antibodies3D8 scFvchemokinemousenuclease activityPRVtherapeutic effects

Identifiers

PMID26255831
PMCPMC4588720
OpenAlexW1176661150

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.