Evidence map›Paper›PMID 28724616›Full record

ArticleThe Journal of experimental medicine2017

Marburg virus survivor immune responses are Th1 skewed with limited neutralizing antibody responses.

Spencer W Stonier, Andrew S Herbert, Ana I Kuehne, Ariel Sobarzo, Polina Habibulin, Chen V Abramovitch Dahan, Rebekah M James, Moses Egesa, Stephen Cose, Julius Julian Lutwama and 2 more

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 27 citations in OpenAlex.

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  6. Quantification of Neutralizing Antibodies in Serum Using VSV-MARV-GFP.Methods in molecular biology (Clifton, N.J.) · 2025
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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

12 authors at 5 institutions in 4 countries.

Spencer W StonierVirology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD.ORCID http://orcid.org/0000-0003-4540-3279
Andrew S HerbertVirology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD.
Ana I KuehneVirology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD.
Ariel SobarzoDepartment of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Polina HabibulinDepartment of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Chen V Abramovitch DahanDepartment of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Rebekah M JamesVirology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD.ORCID http://orcid.org/0000-0001-9370-7555
Moses EgesaUganda Research Unit on AIDS, Medical Research Council/Uganda Virus Research Institute, Entebbe, Uganda.ORCID http://orcid.org/0000-0001-5136-868X
Stephen CoseUganda Research Unit on AIDS, Medical Research Council/Uganda Virus Research Institute, Entebbe, Uganda.ORCID http://orcid.org/0000-0002-5156-037X
Julius Julian LutwamaDepartment of Arbovirology, Emerging, and Re-emerging Infection, Uganda Virus Research Institute, Entebbe, Uganda.
Leslie LobelDepartment of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
John M DyeVirology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD john.m.dye1.civ@mail.mil llobel@bgu.ac.il.ORCID http://orcid.org/0000-0002-0883-5016
United States Army Medical Research Institute of Infectious Diseases · USBen-Gurion University of the Negev · ILLondon School of Hygiene & Tropical Medicine · GBMakerere University · UGUganda Virus Research Institute · UG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Until recently, immune responses in filovirus survivors remained poorly understood. Early studies revealed IgM and IgG responses to infection with various filoviruses, but recent outbreaks have greatly expanded our understanding of filovirus immune responses. Immune responses in survivors of Ebola virus (EBOV) and Sudan virus (SUDV) infections have provided the most insight, with T cell responses as well as detailed antibody responses having been characterized. Immune responses to Marburg virus (MARV), however, remain almost entirely uncharacterized. We report that immune responses in MARV survivors share characteristics with EBOV and SUDV infections but have some distinct differences. MARV survivors developed multivariate CD4

Indexed as

AdolescentAdultAnimalsAntibodies, NeutralizingAntibodies, ViralCD40 LigandCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCytokinesFemaleFlow CytometryHumansImmunity, CellularMaleMarburgvirusMarburg Virus DiseaseAntibodies, NeutralizingAntibodies, ViralCD40 LigandCytokines

Identifiers

PMID28724616
PMCPMC5584125
OpenAlexW2738975296

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.