Evidence map›Paper›PMID 28383105›Full record

ArticleEuropean journal of immunology2017

Enhancement of cytokine-driven NK cell IFN-γ production after vaccination of HCMV infected Africans.

Alansana Darboe, Ebrima Danso, Ed Clarke, Ama Umesi, Ebrima Touray, Rita Wegmuller, Sophie E Moore, Eleanor M Riley, Martin R Goodier

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

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  10. Virus-specific NK cell memory.The Journal of experimental medicine · 2021
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  20. Vaccinating for natural killer cell effector functions.Clinical & translational immunology · 2018
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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

9 authors at 3 institutions in 2 countries.

Alansana DarboeDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, UK.
Ebrima DansoMRC International Nutrition Group, Nutrition Theme, MRC Keneba, Cambridge, UK.
Ed ClarkeVaccine and Immunity Theme, Infant Immunology, Medical Research Council Unit The Gambia, Cambridge, UK.
Ama UmesiVaccine and Immunity Theme, Infant Immunology, Medical Research Council Unit The Gambia, Cambridge, UK.
Ebrima TourayVaccine and Immunity Theme, Infant Immunology, Medical Research Council Unit The Gambia, Cambridge, UK.
Rita WegmullerMRC International Nutrition Group, Nutrition Theme, MRC Keneba, Cambridge, UK.
Sophie E MooreMRC International Nutrition Group, Nutrition Theme, MRC Keneba, Cambridge, UK.
Eleanor M RileyDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, UK.
Martin R GoodierDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, UK.ORCID 0000-0002-1567-8389
MRC Human Nutrition Research · GBMRC Unit the Gambia · GMLondon School of Hygiene & Tropical Medicine · GB

Funding

Medical Research Council G1000808Medical Research Council MC_U123292701Medical Research Council MR/P012019/1
6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) infection drives the phenotypic and functional differentiation of NK cells, thereby influencing the responses of these cells after vaccination. NK cell functional differentiation is particularly advanced in African populations with universal exposure to HCMV. To investigate the impact of advanced differentiation on vaccine-induced responses, we studied NK-cell function before and after vaccination with Trivalent Influenza Vaccine (TIV) or diphtheria, tetanus, pertussis, inactivated poliovirus vaccine (DTPiP) in Africans with universal, lifelong HCMV exposure. In contrast to populations with lower prevalence of HCMV infection, no significant enhancement of NK-cell responses (IFN-γ, CD107a, CD25) occurred after in vitro re-stimulation of post-vaccination NK cells with TIV or DTPiP antigens compared to pre-vaccination baseline cells. However, both vaccinations resulted in higher frequencies of NK cells producing IFN-γ in response to exogenous IL-12 with IL-18, which persisted for up to 6 months. Enhanced cytokine responsiveness was restricted to less differentiated NK cells, with increased frequencies of IFN-γ

Indexed as

AdolescentAdultAfricaAgedChildChild, PreschoolCytomegalovirusCytomegalovirus InfectionsDiphtheria ToxoidFemaleHumansImmunization, SecondaryInfluenza VaccinesInterferon-gammaInterleukin-12Interleukin-18Diphtheria ToxoidDTPolio vaccineIL2RA protein, humanInfluenza VaccinesInterferon-gammaInterleukin-12Interleukin-18Interleukin-2 Receptor alpha SubunitInterleukinsLysosomal-Associated Membrane Protein 1Poliovirus VaccinesTetanus ToxoidVaccines, CombinedDTPiP vaccineInfluenza vaccineNK cellsNKG2CVaccination

Identifiers

PMID28383105
PMCPMC5888140
OpenAlexW2604677144

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.