Evidence map›Paper›PMID 28558022›Full record

ArticlePLoS neglected tropical diseases2017

Different features of Vδ2 T and NK cells in fatal and non-fatal human Ebola infections.

Eleonora Cimini, Domenico Viola, Mar Cabeza-Cabrerizo, Antonella Romanelli, Nicola Tumino, Alessandra Sacchi, Veronica Bordoni, Rita Casetti, Federica Turchi, Federico Martini and 35 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
3.2field-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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. CD4Nature immunology · 2026
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  11. Review
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  14. Article
  15. Depletion but Activation of CD56Virologica Sinica · 2020
    Article
  16. COVID-19: immunopathogenesis and Immunotherapeutics.Signal transduction and targeted therapy · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. 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

45 authors at 14 institutions in 6 countries.

Eleonora CiminiDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Domenico ViolaDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Mar Cabeza-CabrerizoEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Antonella RomanelliDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Nicola TuminoDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Alessandra SacchiDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Veronica BordoniDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Rita CasettiDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Federica TurchiDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Federico MartiniDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Joseph A BoreEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Fara Raymond KoundounoEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Sophie DuraffourEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Janine MichelEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Tobias HolmEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Elsa Gayle ZekengEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Lauren CowleyEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Isabel Garcia DorivalEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Juliane DoerrbeckerEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Nicole HetzeltEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Jonathan H J BaumEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Jasmine PortmannEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Roman WölfelEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Martin GabrielEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Osvaldo MirandaHospital Militar Central Dr. Carlos J. Finlay, Havana, Cuba.
Graciliano DíazHospital Militar Central Dr. Carlos J. Finlay, Havana, Cuba.
José E DíazHospital Militar Central Dr. Carlos J. Finlay, Havana, Cuba.
Yoel A FleitesHospital Militar Central Dr. Carlos J. Finlay, Havana, Cuba.
Carlos A PiñeiroHospital Militar Central Dr. Carlos J. Finlay, Havana, Cuba.
Carlos M CastroHospital Militar Central Dr. Carlos J. Finlay, Havana, Cuba.
Lamine KoivoguiInstitut National de Santé Publique, Conakry, Guinea.
N'Faly MagassoubaLaboratoire des Fièvres Hémorragiques en Guinée, Université Gamal Abdel Nasser de Conakry, Conakry, Guinea.
Boubacar DialloWorld Health Organization, Geneva, Switzerland. (Boubacar is separate: World Health Organization, Conakry, Guinea).
Paula RuibalEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Lisa OestereichEuropean Mobile Laboratory Consortium, Hamburg, Germany.
David M WozniakEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Anja LüdtkeEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Beate Becker-ZiajaEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Maria R CapobianchiDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Giuseppe IppolitoDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
Miles W CarrollEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Stephan GüntherEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Antonino Di CaroDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.
César Muñoz-FontelaEuropean Mobile Laboratory Consortium, Hamburg, Germany.
Chiara AgratiDepartment of Epidemiology and Pre-clinical research, National Institute for Infectious Diseases "Lazzaro Spallanzani", Rome, Italy.ORCID http://orcid.org/0000-0002-5252-0927
Istituto Nazionale per le Malattie Infettive Lazzaro Spallanzani · ITEuropean Molecular Biology Laboratory · DEFinlay Institute · CUGerman Center for Infection Research · DELeibniz Institute of Virology (LIV) · DERobert Koch Institute · DEUniversity of Liverpool · GBGamal Abdel Nasser University of Conakry · GNInstitut National de Santé Publique · GNPublic Health England · GBSouthampton General Hospital · GBSpiez Laboratory · CHUniversität der Bundeswehr München · DEWorld Health Organization · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman Ebola infection is characterized by a paralysis of the immune system. A signature of αβ T cells in fatal Ebola infection has been recently proposed, while the involvement of innate immune cells in the protection/pathogenesis of Ebola infection is unknown. Aim of this study was to analyze γδ T and NK cells in patients from the Ebola outbreak of 2014-2015 occurred in West Africa, and to assess their association with the clinical outcome. METHODOLOGY/PRINCIPAL

findingsNineteen Ebola-infected patients were enrolled at the time of admission to the Ebola Treatment Centre in Guinea. Patients were divided in two groups on the basis of the clinical outcome. The analysis was performed by using multiparametric flow cytometry established by the European Mobile Laboratory in the field. A low frequency of Vδ2 T-cells was observed during Ebola infection, independently from the clinical outcome. Moreover, Vδ2 T-cells from Ebola patients massively expressed CD95 apoptotic marker, suggesting the involvement of apoptotic mechanisms in Vδ2 T-cell loss. Interestingly, Vδ2 T-cells from survivors expressed an effector phenotype and presented a lower expression of the CTLA-4 exhaustion marker than fatalities, suggesting a role of effector Vδ2 T-cells in the protection. Furthermore, patients with fatal Ebola infection were characterized by a lower NK cell frequency than patients with non fatal infection. In particular, both CD56bright and CD56dim NK frequency were very low both in fatal and non fatal infections, while a higher frequency of CD56neg NK cells was associated to non-fatal infections. Finally, NK activation and expression of NKp46 and CD158a were independent from clinical outcome. CONCLUSIONS/SIGNIFICANCES: Altogether, the data suggest that both effector Vδ2 T-cells and NK cells may play a role in the complex network of protective response to EBOV infection. Further studies are required to characterize the protective effector functions of Vδ2 and NK cells.

Indexed as

BiomarkersCD56 AntigenCTLA-4 AntigenDatabases, FactualEbolavirusfas ReceptorFemaleFlow CytometryGuineaHemorrhagic Fever, EbolaHumansKiller Cells, NaturalLymphocyte ActivationMaleNatural Cytotoxicity Triggering Receptor 1Receptors, Antigen, T-Cell, gamma-deltaBiomarkersCD56 AntigenCTLA-4 AntigenFAS protein, humanfas ReceptorNatural Cytotoxicity Triggering Receptor 1NCR1 protein, humanReceptors, Antigen, T-Cell, gamma-deltaReceptors, KIR2DL1

Identifiers

PMID28558022
PMCPMC5472323
OpenAlexW2617891408

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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.