Evidence map›Paper›PMID 32436943›Full record

ArticleThe Journal of infectious diseases2020

Ebola-Specific CD8+ and CD4+ T-Cell Responses in Sierra Leonean Ebola Virus Survivors With or Without Post-Ebola Sequelae.

Stephanie M LaVergne, Saori Sakabe, Lansana Kanneh, Mambu Momoh, Foday Al-Hassan, Mohamed Yilah, Augustine Goba, John Demby Sandi, Michael Gbakie, Beatrice Cubitt and 13 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
0.4field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Metabolic basis of post-infectious sequelae after Ebola virus disease.Metabolomics : Official journal of the Metabolomic Society · 2026
    Article
  4. Article
  5. Review
  6. Metabolic Basis of Post-Infectious Sequelae After Ebola Virus Disease.medRxiv : the preprint server for health sciences · 2026
    Article
  7. Persistent CD8Frontiers in immunology · 2023
    Observational
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. 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

23 authors at 6 institutions in 2 countries.

Stephanie M LaVergneViral-Immunobiology Laboratory, Department of Immunology and Microbiology, Scripps Research, La Jolla, California, USA.
Saori SakabeViral-Immunobiology Laboratory, Department of Immunology and Microbiology, Scripps Research, La Jolla, California, USA.
Lansana KannehViral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
Mambu MomohViral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
Foday Al-HassanViral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
Mohamed YilahViral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
Augustine GobaViral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
John Demby SandiViral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
Michael GbakieViral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
Beatrice CubittViral-Immunobiology Laboratory, Department of Immunology and Microbiology, Scripps Research, La Jolla, California, USA.
Matthew BoisenZalgen Labs, Germantown, USA.
Jessica M MayeuxDepartment of Molecular Medicine, Scripps Research, La Jolla, California, USA.
Ashley SmiraDepartment of Pediatrics, Tulane University School of Medicine, New Orleans, Louisiana, USA.
Kayla ShoreDepartment of Tropical Medicine, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana, USA.
Iris BicaDepartment of Pediatrics, Tulane University School of Medicine, New Orleans, Louisiana, USA.
K Michael PollardDepartment of Molecular Medicine, Scripps Research, La Jolla, California, USA.
Juan Carlos de la TorreViral-Immunobiology Laboratory, Department of Immunology and Microbiology, Scripps Research, La Jolla, California, USA.
Luis M BrancoZalgen Labs, Germantown, USA.
Robert F GarryDepartment of Immunology and Microbiology, Tulane University School of Medicine, New Orleans, Louisiana, USA.
Donald S GrantViral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
John S SchieffelinDepartment of Pediatrics, Tulane University School of Medicine, New Orleans, Louisiana, USA.
Michael B A OldstoneViral-Immunobiology Laboratory, Department of Immunology and Microbiology, Scripps Research, La Jolla, California, USA.
Brian M SullivanViral-Immunobiology Laboratory, Department of Immunology and Microbiology, Scripps Research, La Jolla, California, USA.
Scripps Institution of Oceanography · USTulane University · USUniversity of Sierra Leone · SLMinistry of Health and Sanitation · SLZalgen (United States) · USScripps (United States) · US

Funding

Specific and Broadly Active Monoclonal Antibody Therapeutics Against The FilovirusesU19AI142790 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI ALTER, GALIT · 2019 to 2023
$40.0M
Clinical Sequelae and Urogenital Viral Dynamics in Survivors of Ebola Virus DiseaseR01AI123535 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FISCHER, WILLIAM, WOHL, DAVID A · 2017 to 2021
$3.3M
NIAID NIH HHS HHSN272201400048CNIAID NIH HHS R01 AI123535NIAID NIH HHS U19 AI142790
6 · The paper itself

Abstract

backgroundEbola virus (EBOV) disease has killed thousands of West and Central Africans over the past several decades. Many who survive the acute disease later experience post-Ebola syndrome, a constellation of symptoms whose causative pathogenesis is unclear.

methodsWe investigated EBOV-specific CD8+ and CD4+ T-cell responses in 37 Sierra Leonean EBOV disease survivors with (n = 19) or without (n = 18) sequelae of arthralgia and ocular symptoms. Peripheral blood mononuclear cells were infected with recombinant vesicular stomatitis virus encoding EBOV antigens. We also studied the presence of EBOV-specific immunoglobulin G, antinuclear antibodies, anti-cyclic citrullinated peptide antibodies, rheumatoid factor, complement levels, and cytokine levels in these 2 groups.

resultsSurvivors with sequelae had a significantly higher EBOV-specific CD8+ and CD4+ T-cell response. No differences in EBOV-specific immunoglobulin G, antinuclear antibody, or anti-cyclic citrullinated peptide antibody levels were found. Survivors with sequelae showed significantly higher rheumatoid factor levels.

conclusionEBOV-specific CD8+ and CD4+ T-cell responses were significantly higher in Ebola survivors with post-Ebola syndrome. These findings suggest that pathogenesis may occur as an immune-mediated disease via virus-specific T-cell immune response or that persistent antigen exposure leads to increased and sustained T-cell responses.

Indexed as

AdultAntibodies, ViralAntigens, ViralCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesEbolavirusFemaleFluorescent Antibody TechniqueHemorrhagic Fever, EbolaHumansImmunity, CellularMaleSierra LeoneSurvivorsAntibodies, ViralAntigens, ViralEbola viruspost-Ebola sequelaeT-cell response

Identifiers

PMID32436943
PMCPMC7529037
OpenAlexW3026863081

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.