Evidence map›Paper›PMID 27109916›Full record

ArticleScientific reports2016

Production of Potent Fully Human Polyclonal Antibodies against Ebola Zaire Virus in Transchromosomal Cattle.

John M Dye, Hua Wu, Jay W Hooper, Surender Khurana, Ana I Kuehne, Elizabeth M Coyle, Ramon A Ortiz, Sandra Fuentes, Andrew S Herbert, Hana Golding and 13 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 43 citations in OpenAlex.

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  9. The contribution of bovines to human health against viral infections.Environmental science and pollution research international · 2021
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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

23 authors at 7 institutions in 1 country.

John M DyeVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Hua WuSAB Biotherapeutics, Sioux Falls, South Dakota, United States of America.
Jay W HooperVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Surender KhuranaDivision of Viral Products, Center for Biologics Evaluation and Research (CBER), Food and Drug Administration, Silver Spring, Maryland, USA.
Ana I KuehneVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Elizabeth M CoyleDivision of Viral Products, Center for Biologics Evaluation and Research (CBER), Food and Drug Administration, Silver Spring, Maryland, USA.
Ramon A OrtizVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Sandra FuentesDivision of Viral Products, Center for Biologics Evaluation and Research (CBER), Food and Drug Administration, Silver Spring, Maryland, USA.
Andrew S HerbertVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Hana GoldingDivision of Viral Products, Center for Biologics Evaluation and Research (CBER), Food and Drug Administration, Silver Spring, Maryland, USA.
Russell A BakkenVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Jennifer M BrannanVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Steve A KwilasVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA.
Eddie J SullivanSAB Biotherapeutics, Sioux Falls, South Dakota, United States of America.
Thomas C LukeViral and Rickettsial Diseases Department, Navy Medical Research Center, The Henry Jackson Foundation, Silver Spring, Maryland, USA.
Gale SmithNovavax Inc, Gaithersburg, Maryland, USA.
Gregory GlennNovavax Inc, Gaithersburg, Maryland, USA.
Wenfang LiDepartment of Microbiology and Immunology and Emory Vaccine Center, Emory University, Atlanta, Georgia, 30322, USA.
Ling YeDepartment of Microbiology and Immunology and Emory Vaccine Center, Emory University, Atlanta, Georgia, 30322, USA.
Chinglai YangDepartment of Microbiology and Immunology and Emory Vaccine Center, Emory University, Atlanta, Georgia, 30322, USA.
Richard W CompansDepartment of Microbiology and Immunology and Emory Vaccine Center, Emory University, Atlanta, Georgia, 30322, USA.
Ralph A TrippThe University of Georgia, Athens, Georgia, 30602, USA.
Jin-An JiaoSAB Biotherapeutics, Sioux Falls, South Dakota, United States of America.
United States Army Medical Research Institute of Infectious Diseases · USCenter for Biologics Evaluation and Research · USEmory University · USSab Biotherapeutics (United States) · USNovavax (United States) · USJackson Foundation · USUniversity of Georgia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyclonal antibodies, derived from humans or hyperimmunized animals, have been used prophylactically or therapeutically as countermeasures for a variety of infectious diseases. SAB Biotherapeutics has successfully developed a transchromosomic (Tc) bovine platform technology that can produce fully human immunoglobulins rapidly, and in substantial quantities, against a variety of disease targets. In this study, two Tc bovines expressing high levels of fully human IgG were hyperimmunized with a recombinant glycoprotein (GP) vaccine consisting of the 2014 Ebola virus (EBOV) Makona isolate. Serum collected from these hyperimmunized Tc bovines contained high titers of human IgG against EBOV GP as determined by GP specific ELISA, surface plasmon resonance (SPR), and virus neutralization assays. Fully human polyclonal antibodies against EBOV were purified and evaluated in a mouse challenge model using mouse adapted Ebola virus (maEBOV). Intraperitoneal administration of the purified anti-EBOV IgG (100 mg/kg) to BALB/c mice one day after lethal challenge with maEBOV resulted in 90% protection; whereas 100% of the control animals succumbed. The results show that hyperimmunization of Tc bovines with EBOV GP can elicit protective and potent neutralizing fully human IgG antibodies rapidly and in commercially viable quantities.

Indexed as

Animals, Genetically ModifiedCattleAnimalsAntibodies, ViralDisease Models, AnimalEbolavirusEnzyme-Linked Immunosorbent AssayHemorrhagic Fever, EbolaHumansImmunization, PassiveImmunoglobulin GMice, Inbred BALB CNeutralization TestsSurface Plasmon ResonanceTreatment OutcomeAntibodies, ViralImmunoglobulin G

Identifiers

PMID27109916
PMCPMC4842964
OpenAlexW2344155554

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.