Evidence map›Paper›PMID 26715676›Full record

ArticleThe Journal of infectious diseases2016

Development of a Cost-effective Ovine Polyclonal Antibody-Based Product, EBOTAb, to Treat Ebola Virus Infection.

Stuart David Dowall, Jo Callan, Antra Zeltina, Ibrahim Al-Abdulla, Thomas Strecker, Sarah K Fehling, Verena Krähling, Andrew Bosworth, Emma Rayner, Irene Taylor and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

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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

17 authors at 4 institutions in 3 countries.

Stuart David DowallPublic Health England, Salisbury.
Jo CallanMicroPharm, Newcastle Emlyn.
Antra ZeltinaDivision of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, United Kingdom.
Ibrahim Al-AbdullaMicroPharm, Newcastle Emlyn.
Thomas StreckerInstitute of Virology, Philipps University Marburg, Germany.
Sarah K FehlingInstitute of Virology, Philipps University Marburg, Germany.
Verena KrählingInstitute of Virology, Philipps University Marburg, Germany.
Andrew BosworthPublic Health England, Salisbury.
Emma RaynerPublic Health England, Salisbury.
Irene TaylorPublic Health England, Salisbury.
Sue CharltonPublic Health England, Salisbury.
John LandonMicroPharm, Newcastle Emlyn.
Ian CameronMicroPharm, Newcastle Emlyn.
Roger HewsonPublic Health England, Salisbury.
Abdulsalami NasidiNigerian Centre for Disease Control, Abuja.
Thomas A BowdenDivision of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, United Kingdom.
Miles W CarrollPublic Health England, Salisbury.
Public Health England · GBPhilipps University of Marburg · DEUniversity of Oxford · GBNigeria Centre for Disease Control · NG

Funding

Medical Research Council MR/L009528/1Wellcome TrustWellcome Trust 090532/Z/09/Z
6 · The paper itself

Abstract

The highly glycosylated glycoprotein spike of Ebola virus (EBOV-GP1,2) is the primary target of the humoral host response. Recombinant EBOV-GP ectodomain (EBOV-GP1,2ecto) expressed in mammalian cells was used to immunize sheep and elicited a robust immune response and produced high titers of high avidity polyclonal antibodies. Investigation of the neutralizing activity of the ovine antisera in vitro revealed that it neutralized EBOV. A pool of intact ovine immunoglobulin G, herein termed EBOTAb, was prepared from the antisera and used for an in vivo guinea pig study. When EBOTAb was delivered 6 hours after challenge, all animals survived without experiencing fever or other clinical manifestations. In a second series of guinea pig studies, the administration of EBOTAb dosing was delayed for 48 or 72 hours after challenge, resulting in 100% and 75% survival, respectively. These studies illustrate the usefulness of EBOTAb in protecting against EBOV-induced disease.

Indexed as

AnimalsAntibodies, ViralCost-Benefit AnalysisEbolavirusFemaleGene Expression Regulation, ViralGlycoproteinsGuinea PigsHEK293 CellsHemorrhagic Fever, EbolaHumansImmunoglobulin GMembrane GlycoproteinsProtein BindingProtein Structure, TertiarySheepAntibodies, ViralGlycoproteinsImmunoglobulin GMembrane GlycoproteinsantibodyEbolaefficacyneutralizationtherapeutic

Identifiers

PMID26715676
PMCPMC4779302
OpenAlexW2231078147

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.