Evidence map›Paper›PMID 31052499›Full record

ReviewViruses2019

Extracellular Vesicles and Ebola Virus: A New Mechanism of Immune Evasion.

Michelle L Pleet, Catherine DeMarino, Spencer W Stonier, John M Dye, Steven Jacobson, M Javad Aman, Fatah Kashanchi

Open access · goldAbstract readReview
In one paragraph

Review in Viruses, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Rational design of self-amplifying virus-like vesicles with Ebola virus glycoprotein as vaccines.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  6. Extracellular Vesicles: The Invisible Heroes and Villains of COVID-19 Central Neuropathology.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  7. Review
  8. Review
  9. Exosomal transmission of viruses, a two-edged biological sword.Cell communication and signaling : CCS · 2023
    Review
  10. Extracellular Vesicles and Viruses: Two Intertwined Entities.International journal of molecular sciences · 2023
    Review
  11. Extracellular vesicle storm during the course of Ebola virus infection in primates.Frontiers in cellular and infection microbiology · 2023
    Article
  12. Review
  13. Hyperinflammation, apoptosis, and organ damage.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Putative Roles for Peptidylarginine Deiminases in COVID-19.International journal of molecular sciences · 2020
    Article
  19. Extracellular Vesicle-Related Thrombosis in Viral Infection.International journal of general medicine · 2020
    Review
  20. Cloaked Viruses and Viral Factors in Cutting Edge Exosome-Based Therapies.Frontiers in cell and developmental biology · 2020
    Review
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

7 authors at 4 institutions in 1 country.

Michelle L PleetLaboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA 20110, USA. mpleet@gmu.edu.
Catherine DeMarinoLaboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA 20110, USA. cdemarin@gmu.edu.
Spencer W StonierDepartment, Emergent BioSolutions, Gaithersburg, MD 20879, USA. stoniers@ebsi.com.
John M DyeVirology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA. john.m.dye1.civ@mail.mil.
Steven JacobsonViral Immunology Section, Neuroimmunology Branch, National Institute for Neurological Disease and Stroke, National Institutes of Health, Bethesda, MD, 20892, USA. jacobsons@ninds.nih.gov.
M Javad AmanDepartment. Integrated BioTherapeutics, Inc., Gaithersburg, MD 20850, USA. jaman@integratedbiotherapeutics.com.
Fatah KashanchiLaboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA 20110, USA. fkashanc@gmu.edu.
George Mason University · USUnited States Army Medical Research Institute of Infectious Diseases · USIntegrated BioTherapeutics (United States) · USNational Institutes of Health · US

Funding

Rationally Designed Pan-Ebolavirus VaccineR01AI132204 · NIAID · INTEGRATED BIOTHERAPEUTICS, INC. · PI AMAN, M JAVAD, SAPHIRE, ERICA OLLMANN · 2017 to 2021
$6.6M
HIV1 INHIBITION USING TAT PEPTIDE DERIVATIVESR01AI043894 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI KASHANCHI, FATAH · 1999 to 2015
$4.4M
HIV neuropathogenesis related to exosomes containing HIV non-coding RNAsR01NS099029 · NINDS · GEORGE MASON UNIVERSITY · PI KASHANCHI, FATAH · 2016 to 2020
$1.9M
Effect of chromatin remodelers/modifiers on HIV-1 Tat activated transcriptionR21AI074410 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI KASHANCHI, FATAH · 2009 to 2010
$432k
A radiation-induced cellular stress activates HIV and induces killing of infected cellsR21AI127351 · NIAID · GEORGE MASON UNIVERSITY · PI KASHANCHI, FATAH · 2016 to 2017
$418k
HIV-1 TAR derived miRNA: Implications for Latency and PathogenesisR21AI078859 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI KASHANCHI, FATAH · 2009 to 2010
$400k
NIAID NIH HHS R01 AI043894NIAID NIH HHS R01 AI132204NIAID NIH HHS R21 AI074410NIAID NIH HHS R21 AI078859NIAID NIH HHS R21 AI127351NIH HHS AI043894NIH HHS AI074410NIH HHS AI078859NIH HHS AI127351-01NIH HHS NS099029NINDS NIH HHS R01 NS099029
6 · The paper itself

Abstract

Ebola virus (EBOV) disease can result in a range of symptoms anywhere from virtually asymptomatic to severe hemorrhagic fever during acute infection. Additionally, spans of asymptomatic persistence in recovering survivors is possible, during which transmission of the virus may occur. In acute infection, substantial cytokine storm and bystander lymphocyte apoptosis take place, resulting in uncontrolled, systemic inflammation in affected individuals. Recently, studies have demonstrated the presence of EBOV proteins VP40, glycoprotein (GP), and nucleoprotein (NP) packaged into extracellular vesicles (EVs) during infection. EVs containing EBOV proteins have been shown to induce apoptosis in recipient immune cells, as well as contain pro-inflammatory cytokines. In this manuscript, we review the current field of knowledge on EBOV EVs including the mechanisms of their biogenesis, their cargo and their effects in recipient cells. Furthermore, we discuss some of the effects that may be induced by EBOV EVs that have not yet been characterized and highlight the remaining questions and future directions.

Indexed as

Host-Pathogen InteractionsAnimalsBystander EffectCell CycleCytokinesEbolavirusExosomesExtracellular VesiclesHemorrhagic Fever, EbolaHumansImmune EvasionNucleoproteinsViral Core ProteinsViral Matrix ProteinsCytokinesNucleoproteinsnucleoprotein VP40, Ebola virusViral Core ProteinsViral Matrix ProteinscytokineEbola virusexosomeextracellular vesiclesGPNPVP40

Identifiers

PMID31052499
PMCPMC6563240
OpenAlexW2942903069

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.