Evidence map›Paper›PMID 28381540›Full record

ArticleScience translational medicine2017

Therapeutic treatment of Marburg and Ravn virus infection in nonhuman primates with a human monoclonal antibody.

Chad E Mire, Joan B Geisbert, Viktoriya Borisevich, Karla A Fenton, Krystle N Agans, Andrew I Flyak, Daniel J Deer, Herta Steinkellner, Ognian Bohorov, Natasha Bohorova and 9 more

Abstract read
In one paragraph

Article in Science translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

66 citing papers in PubMed, 92 citations in OpenAlex.

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  16. Marburg Virus Medical Countermeasures.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
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  18. Article
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6 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

19 authors at 4 institutions in 2 countries.

Chad E MireGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.ORCID 0000-0001-7596-1808
Joan B GeisbertGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.ORCID 0000-0003-0858-1877
Viktoriya BorisevichGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.
Karla A FentonGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.
Krystle N AgansGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.
Andrew I FlyakDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0002-8722-479X
Daniel J DeerGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.
Herta SteinkellnerDepartment of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, 1190 Vienna, Austria.ORCID 0000-0003-4823-1505
Ognian BohorovMapp Biopharmaceutical Inc., San Diego, CA 92121, USA.
Natasha BohorovaMapp Biopharmaceutical Inc., San Diego, CA 92121, USA.
Charles GoodmanMapp Biopharmaceutical Inc., San Diego, CA 92121, USA.
Andrew HiattMapp Biopharmaceutical Inc., San Diego, CA 92121, USA.
Do H KimMapp Biopharmaceutical Inc., San Diego, CA 92121, USA.ORCID 0000-0002-2725-4153
Michael H PaulyMapp Biopharmaceutical Inc., San Diego, CA 92121, USA.
Jesus VelascoMapp Biopharmaceutical Inc., San Diego, CA 92121, USA.
Kevin J WhaleyDepartment of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, 1190 Vienna, Austria.
James E CroweDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.ORCID 0000-0002-0049-1079
Larry ZeitlinMapp Biopharmaceutical Inc., San Diego, CA 92121, USA. twgeisbe@utmb.edu larry.zeitlin@mappbio.com.ORCID 0000-0002-6857-1024
Thomas W GeisbertGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA. twgeisbe@utmb.edu larry.zeitlin@mappbio.com.ORCID 0000-0003-0858-1877
Mapp Biopharmaceutical (United States) · USThe University of Texas Medical Branch at Galveston · USBOKU University · ATVanderbilt University Medical Center · US

Funding

Regulatory Compliance Core - Galveston National Laboratory BSL4 OperationsUC7AI094660 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI Dennis A Bente · 2011 to 2026
$208.8M
Mechanistic Virology CoreU19AI109762 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI LAI, JONATHAN R. · 2014 to 2018
$29.6M
Supplemental Research Project (SRP)U19AI109711 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI GEISBERT, THOMAS WILLIAM · 2014 to 2018
$26.6M
MR191_ An Immunoprotectant for Marburg VirusSB1AI082744 · NIAID · MAPP BIOPHARMACEUTICAL, INC. · PI AIMES, RONALD T · 2017 to 2019
$3.0M
An Immunoprotectant for Marburg VirusR44AI082744 · NIAID · MAPP BIOPHARMACEUTICAL, INC. · PI ZEITLIN, LARRY · 2014 to 2016
$3.0M
An Immunoprotectant for Marburg VirusR43AI082744 · NIAID · MAPP BIOPHARMACEUTICAL, INC. · PI ZEITLIN, LARRY · 2009 to 2010
$525k
NIAID NIH HHS R43 AI082744NIAID NIH HHS R44 AI082744NIAID NIH HHS SB1 AI082744NIAID NIH HHS U19 AI109711NIAID NIH HHS U19 AI109762NIAID NIH HHS UC7 AI094660
6 · The paper itself

Abstract

As observed during the 2013-2016 Ebola virus disease epidemic, containment of filovirus outbreaks is challenging and made more difficult by the lack of approved vaccine or therapeutic options. Marburg and Ravn viruses are highly virulent and cause severe and frequently lethal disease in humans. Monoclonal antibodies (mAbs) are a platform technology in wide use for autoimmune and oncology indications. Previously, we described human mAbs that can protect mice from lethal challenge with Marburg virus. We demonstrate that one of these mAbs, MR191-N, can confer a survival benefit of up to 100% to Marburg or Ravn virus-infected rhesus macaques when treatment is initiated up to 5 days post-inoculation. These findings extend the small but growing body of evidence that mAbs can impart therapeutic benefit during advanced stages of disease with highly virulent viruses and could be useful in epidemic settings.

Indexed as

AnimalsAntibodies, MonoclonalCross ProtectionFiloviridaeFiloviridae InfectionsGuinea PigsHumansMacaca fascicularisMacaca mulattaMarburgvirusMarburg Virus DiseasePilot ProjectsAntibodies, Monoclonal

Identifiers

PMID28381540
PMCPMC5719873
OpenAlexW2604139512

What OpenQuestion holds

Textmetadata
LicenceTDM
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.