Evidence map›Paper›PMID 28404864›Full record

ArticleScience translational medicine2017

Longitudinal peripheral blood transcriptional analysis of a patient with severe Ebola virus disease.

John C Kash, Kathie-Anne Walters, Jason Kindrachuk, David Baxter, Kelsey Scherler, Krisztina B Janosko, Rick D Adams, Andrew S Herbert, Rebekah M James, Spencer W Stonier and 5 more

Open access · greenAbstract 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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.9field-weighted citation impact, top 9% 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, 29 citations in OpenAlex.

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  17. Evidence of Ebola Virus Replication and High Concentration in Semen of a Patient During Recovery.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2017
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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

15 authors at 3 institutions in 1 country.

John C KashViral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-8037-7101
Kathie-Anne WaltersInstitute for Systems Biology, Seattle, WA 98109, USA.ORCID 0000-0003-1547-6397
Jason KindrachukCritical Care Medicine Department, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-3305-7084
David BaxterInstitute for Systems Biology, Seattle, WA 98109, USA.ORCID 0000-0003-4468-2069
Kelsey ScherlerInstitute for Systems Biology, Seattle, WA 98109, USA.ORCID 0000-0001-5955-5391
Krisztina B JanoskoIntegrated Research Facility, Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD 21702, USA.ORCID 0000-0002-7624-2167
Rick D AdamsIntegrated Research Facility, Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, MD 21702, USA.ORCID 0000-0002-6906-4403
Andrew S HerbertUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA.ORCID 0000-0003-4697-7928
Rebekah M JamesUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA.ORCID 0000-0001-9370-7555
Spencer W StonierUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA.ORCID 0000-0003-4540-3279
Matthew J MemoliViral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
John M DyeUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA.ORCID 0000-0002-0883-5016
Richard T DaveyLaboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Daniel S ChertowCritical Care Medicine Department, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-1675-1728
Jeffery K TaubenbergerViral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA. taubenbergerj@niaid.nih.gov.ORCID 0000-0002-9694-7228
National Institutes of Health · USUnited States Army Medical Research Institute of Infectious Diseases · USInstitute for Systems Biology · US

Funding

Influenza and Emerging Infectious DiseasesZIAAI000984 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DAVEY, RICHARD · 2009 to 2025
$44.1M
Pandemic Influenza Translational Research; Novel Vaccine and Drug TherapyZIAAI001157 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MEMOLI, MATTHEW · 2012 to 2025
$37.2M
Influenza Viral PathogenesisZIAAI000986 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI TAUBENBERGER, JEFFERY · 2009 to 2025
$30.0M
Clinical and Molecular Features of Ebola Virus DiseaseZIACL009024 · CLC · CLINICAL CENTER · PI CHERTOW, DANIEL S · 2017 to 2025
$0k
Intramural NIH HHS ZIA AI000986
6 · The paper itself

Abstract

The 2013-2015 outbreak of Ebola virus disease in Guinea, Liberia, and Sierra Leone was unprecedented in the number of documented cases, but there have been few published reports on immune responses in clinical cases and their relationships with the course of illness and severity of Ebola virus disease. Symptoms of Ebola virus disease can include severe headache, myalgia, asthenia, fever, fatigue, diarrhea, vomiting, abdominal pain, and hemorrhage. Although experimental treatments are in development, there are no current U.S. Food and Drug Administration-approved vaccines or therapies. We report a detailed study of host gene expression as measured by microarray in daily peripheral blood samples collected from a patient with severe Ebola virus disease. This individual was provided with supportive care without experimental therapies at the National Institutes of Health Clinical Center from before onset of critical illness to recovery. Pearson analysis of daily gene expression signatures revealed marked gene expression changes in peripheral blood leukocytes that correlated with changes in serum and peripheral blood leukocytes, viral load, antibody responses, coagulopathy, multiple organ dysfunction, and then recovery. This study revealed marked shifts in immune and antiviral responses that preceded changes in medical condition, indicating that clearance of replicating Ebola virus from peripheral blood leukocytes is likely important for systemic viral clearance.

Indexed as

Disease OutbreaksEbolavirusHemorrhagic Fever, EbolaHumansLeukocytesLongitudinal StudiesRNA, ViralVirus ReplicationRNA, Viral

Identifiers

PMID28404864
PMCPMC5497219
OpenAlexW2606681775

What OpenQuestion holds

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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.