Evidence map›Paper›PMID 32413101›Full record

Trial reportThe Journal of experimental medicine2020

Reduced Ebola vaccine responses in CMV+ young adults is associated with expansion of CD57+KLRG1+ T cells.

Georgina Bowyer, Hannah Sharpe, Navin Venkatraman, Pierre Birahim Ndiaye, Djibril Wade, Nicole Brenner, Alex Mentzer, Catherine Mair, Tim Waterboer, Teresa Lambe and 4 more

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in The Journal of experimental medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
0.8field-weighted citation impact, top 16% 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

35 citing papers in PubMed, 52 citations in OpenAlex.

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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

14 authors at 3 institutions in 3 countries.

Georgina BowyerThe Jenner Institute, University of Oxford, Oxford, UK.
Hannah SharpeThe Jenner Institute, University of Oxford, Oxford, UK.
Navin VenkatramanThe Jenner Institute, University of Oxford, Oxford, UK.
Pierre Birahim NdiayeCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Djibril WadeCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Nicole BrennerInfections and Cancer Epidemiology, German Cancer Research Center, Heidelberg, Germany.
Alex MentzerThe Jenner Institute, University of Oxford, Oxford, UK.
Catherine MairThe Jenner Institute, University of Oxford, Oxford, UK.
Tim WaterboerInfections and Cancer Epidemiology, German Cancer Research Center, Heidelberg, Germany.
Teresa LambeThe Jenner Institute, University of Oxford, Oxford, UK.
Tandakha DieyeCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Souleymane MboupCentre Hospitalier Universitaire le Dantec, Dakar, Senegal.
Adrian V S HillThe Jenner Institute, University of Oxford, Oxford, UK.
Katie J EwerThe Jenner Institute, University of Oxford, Oxford, UK.
University of Oxford · GBHôpital Aristide Le Dantec · SNGerman Cancer Research Center · DE

Funding

Department of HealthMedical Research Council MR/R005850/1Wellcome Trust
6 · The paper itself

Abstract

CMV is associated with immunosenescence and reduced vaccine responses in the elderly (>70 yr). However, the impact of CMV in young adults is less clear. In this study, healthy UK and Senegalese adults aged 18-50 yr (average, 29 yr) were vaccinated with the Ebola vaccine candidate chimpanzee adenovirus type 3-vectored Ebola Zaire vaccine (ChAd3-EBO-Z) and boosted with modified vaccinia Ankara Ebola Zaire-vectored (MVA-EBO-Z) vaccine. CMV carriage was associated with an expansion of phenotypically senescent CD4+ and CD8+ T cells expressing CD57 and killer cell lectin-like receptor G1 (KLRG1), which was negatively associated with vaccine responses in both cohorts. Ebola-specific T cell responses induced by vaccination also contained significantly increased frequencies of terminally differentiated CD57+KLRG1+ cells in CMV seropositive (CMV+) individuals. This study suggests that CMV can also affect vaccine responses in younger adults and may have a particularly marked impact in many developing countries where CMV seroprevalence is almost universal.

Indexed as

AdultCD4-Positive T-LymphocytesCD57 AntigensCD8-Positive T-LymphocytesCell DifferentiationCell ProliferationCellular SenescenceCytomegalovirus InfectionsEbola VaccinesHumansImmunologic MemoryLectins, C-TypeMiddle AgedPhenotypeReceptors, ImmunologicSeroepidemiologic StudiesCD57 AntigensEbola VaccinesKLRG1 protein, humanLectins, C-TypeReceptors, Immunologic

Identifiers

PMID32413101
PMCPMC7336307
OpenAlexW3024419295

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.