Evidence map›Paper›PMID 29195741›Full record

ArticleCellular immunology2018

Ebola virus secreted glycoprotein decreases the anti-viral immunity of macrophages in early inflammatory responses.

Jillian H Bradley, Ametria Harrison, Ashley Corey, Nathan Gentry, Randal K Gregg

Open access · greenAbstract read
In one paragraph

Article in Cellular immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Ebola virus-like particles reprogram cellular metabolism.Journal of molecular medicine (Berlin, Germany) · 2023
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Mechanisms of Immune Evasion by Ebola Virus.Advances in experimental medicine and biology · 2021
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. 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

5 authors at 2 institutions in 1 country.

Jillian H BradleyDivision of Biomedical Sciences, Magnolia Research Center, Department of Microbiology and Immunology, Edward Via College of Osteopathic Medicine - Carolinas Campus, Spartanburg, SC 29303, United States.
Ametria HarrisonDepartment of Biology, Chemistry and Physics, Converse College, Spartanburg, SC 29301, United States.
Ashley CoreyDivision of Biomedical Sciences, Magnolia Research Center, Department of Microbiology and Immunology, Edward Via College of Osteopathic Medicine - Carolinas Campus, Spartanburg, SC 29303, United States.
Nathan GentryDivision of Biomedical Sciences, Magnolia Research Center, Department of Microbiology and Immunology, Edward Via College of Osteopathic Medicine - Carolinas Campus, Spartanburg, SC 29303, United States.
Randal K GreggDivision of Biomedical Sciences, Magnolia Research Center, Department of Microbiology and Immunology, Edward Via College of Osteopathic Medicine - Carolinas Campus, Spartanburg, SC 29303, United States. Electronic address: rgregg@carolinas.vcom.edu.
Edward Via College of Osteopathic Medicine · USConverse College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During Ebola virus (EBOV) infection, secreted glycoprotein (sGP) is found in large quantities in the serum of both patients and infected animal models. It is thought to serve as a decoy for anti-EBOV antibodies. Using an in vitro model incorporating treatment of non-infected human THP-1 macrophages with recombinant EBOV sGP, this study sought to examine the impact of sGP upon key macrophage functions. Macrophage polarization and phagocytic capacity of activated macrophages were found to be unaltered by sGP treatment. However, treatment with sGP inhibited macrophage production of the pro-inflammatory cytokines TNFα and IL-6 while the yield of anti-inflammatory cytokine, IL-10, remained intact. Interestingly, the migratory ability of macrophages was also diminished by sGP, potentially due to a decrease in expression of CD11b, a vital macrophage integrin. Thus, EBOV sGP may operate to diminish functional contributions of non-infected macrophages to increase the potential viral dissemination.

Indexed as

Antibodies, ViralAntiviral AgentsCytokinesEbolavirusGlycoproteinsHemorrhagic Fever, EbolaHumansMacrophagesMonocytesTHP-1 CellsViral ProteinsAntibodies, ViralAntiviral AgentsCytokinesGlycoproteinssecreted glycoprotein, Ebola virusViral ProteinsChemotaxisCytokineEbola virusMacrophagePhagocytosisSecreted glycoproteinViral immune evasion

Identifiers

PMID29195741
PMCPMC7094302
OpenAlexW2769548746

What OpenQuestion holds

Textmetadata
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.