Evidence map›Paper›PMID 26874822›Full record

ArticleClinical and experimental immunology2016

Expansion of highly activated invariant natural killer T cells with altered phenotype in acute dengue infection.

A Kamaladasa, N Wickramasinghe, T N Adikari, L Gomes, N L A Shyamali, M Salio, V Cerundolo, G S Ogg, G Neelika Malavige

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In one paragraph

Article in Clinical and experimental immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
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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 4 institutions in 2 countries.

A KamaladasaDepartment of Microbiology, Centre for Dengue Research, University of Sri Jayawardanapura, Sri Lanka.
N WickramasingheDepartment of Microbiology, Centre for Dengue Research, University of Sri Jayawardanapura, Sri Lanka.
T N AdikariDepartment of Microbiology, Centre for Dengue Research, University of Sri Jayawardanapura, Sri Lanka.
L GomesDepartment of Microbiology, Centre for Dengue Research, University of Sri Jayawardanapura, Sri Lanka.
N L A ShyamaliDepartment of Medicine, Faculty of Medical Sciences, University of Sri Jayawardanapura, Sri Lanka.
M SalioMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
V CerundoloMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
G S OggMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
G Neelika MalavigeDepartment of Microbiology, Centre for Dengue Research, University of Sri Jayawardanapura, Sri Lanka.
University of Sri Jayewardenepura · LKMRC Human Immunology Unit · GBChurchill Hospital · GBUniversity of Oxford · GB

Funding

Cancer Research UK 11331Cancer Research UK 17722Cancer Research UK C399/A2291Medical Research Council G1000800Medical Research Council MC_UU_12010/1Medical Research Council MC_UU_12010/5
6 · The paper itself

Abstract

Invariant natural killer T (iNKT) cells are capable of rapid activation and production of cytokines upon recognition of antigenic lipids presented by CD1d molecules. They have been shown to play a significant role in many viral infections and were observed to be highly activated in patients with acute dengue infection. In order to characterize further their role in dengue infection, we investigated the proportion of iNKT cells and their phenotype in adult patients with acute dengue infection. The functionality of iNKT cells in patients was investigated by both interferon (IFN)-γ and interleukin (IL)-4 ex-vivo enzyme-linked immunospot (ELISPOT) assays following stimulation with alpha-galactosyl-ceramide (αGalCer). We found that circulating iNKT cell proportions were significantly higher (P = 0·03) in patients with acute dengue when compared to healthy individuals and were predominantly of the CD4(+) subset. iNKT cells of patients with acute dengue had reduced proportions expressing CD8α and CD161 when compared to healthy individuals. The iNKT cells of patients were highly activated and iNKT activation correlated significantly with dengue virus-specific immunoglobulin (Ig)G antibody levels. iNKT cells expressing Bcl-6 (P = 0·0003) and both Bcl-6 and inducible T cell co-stimulator (ICOS) (P = 0·006) were increased significantly in patients when compared to healthy individuals. Therefore, our data suggest that in acute dengue infection there is an expansion of highly activated CD4(+) iNKT cells, with reduced expression of CD161 markers.

Indexed as

Lymphocyte ActivationAcute DiseaseAdultAntibodies, ViralCD8 AntigensDengueDengue VirusEnzyme-Linked Immunospot AssayFemaleGalactosylceramidesHumansImmunoglobulin GInducible T-Cell Co-Stimulator ProteinInterferon-gammaInterleukin-4Lymphocyte Countalpha-galactosylceramideAntibodies, ViralBCL6 protein, humanCD8 antigen, alpha chainCD8 AntigensGalactosylceramidesIL4 protein, humanImmunoglobulin GInducible T-Cell Co-Stimulator ProteinInterferon-gammaInterleukin-4KLRB1 protein, humanNK Cell Lectin-Like Receptor Subfamily BProto-Oncogene Proteins c-bcl-6

Identifiers

PMID26874822
PMCPMC4954999
OpenAlexW2487793776

What OpenQuestion holds

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Registered trials

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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.