Evidence map›Paper›PMID 25359276›Full record

ArticleEuropean journal of immunology2015

Peptide selectivity discriminates NK cells from KIR2DL2- and KIR2DL3-positive individuals.

Sorcha Cassidy, Sayak Mukherjee, Thet Mon Myint, Berenice Mbiribindi, Helen North, James Traherne, Arend Mulder, Frans H J Claas, Marco A Purbhoo, Jayajit Das and 1 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Natural killer cells in multiple sclerosis: foe or friends?Frontiers in cellular neuroscience · 2025
    Review
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  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Cattle NK Cell Heterogeneity and the Influence of MHC Class I.Journal of immunology (Baltimore, Md. : 1950) · 2015
    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

11 authors at 7 institutions in 3 countries.

Sorcha CassidyClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, UK; Division of Medicine, Imperial College London, London, UK.
Sayak Mukherjee
Thet Mon Myint
Berenice Mbiribindi
Helen North
James Traherne
Arend Mulder
Frans H J Claas
Marco A Purbhoo
Jayajit Das
Salim I Khakoo
Imperial College London · GBLeiden University Medical Center · NLNHS Blood and Transplant · GBBattelle · USThe Ohio State University · USUniversity of Cambridge · GBUniversity of Southampton · GB

Funding

A computational model to uncover basic signaling mechanisms of NK cell activationR56AI090115 · NIAID · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI DAS, JAYAJIT · 2012 to 2012
$186k
Medical Research Council G1001738NIAID NIH HHS 1R56AI090115-01A1NIAID NIH HHS R56 AI090115Wellcome TrustWellcome Trust WT076991MAWellcome Trust WT089883MAWellcome Trust WT093465MA
6 · The paper itself

Abstract

Natural killer cells are controlled by peptide selective inhibitory receptors for MHC class I, including the killer cell immunoglobulin-like receptors (KIRs). Despite having similar ligands, KIR2DL2 and KIR2DL3 confer different levels of protection to infectious disease. To investigate how changes in peptide repertoire may differentially affect NK cell reactivity, NK cells from KIR2DL2 and KIR2DL3 homozygous donors were tested for activity against different combinations of strong inhibitory (VAPWNSFAL), weak inhibitory (VAPWNSRAL), and antagonist peptide (VAPWNSDAL). KIR2DL3-positive NK cells were more sensitive to changes in the peptide content of MHC class I than KIR2DL2-positive NK cells. These differences were observed for the weakly inhibitory peptide VAPWNSRAL in single peptide and double peptide experiments (p < 0.01 and p < 0.03, respectively). More significant differences were observed in experiments using all three peptides (p < 0.0001). Mathematical modeling of the experimental data demonstrated that VAPWNSRAL was dominant over VAPWNSFAL in distinguishing KIR2DL3- from KIR2DL2-positive donors. Donors with different KIR genotypes have different responses to changes in the peptide bound by MHC class I. Differences in the response to the peptide content of MHC class I may be one mechanism underlying the protective effects of different KIR genes against infectious disease.

Indexed as

Models, StatisticalAmino Acid SequenceCell DegranulationGene Expression RegulationGenotypeHLA-C AntigensHomozygoteHumansKiller Cells, NaturalLigandsMolecular Sequence DataPeptidesPrimary Cell CultureProtein BindingReceptors, KIR2DL2Receptors, KIR2DL3HLA-C AntigensKIR2DL2 protein, humanKIR2DL3 protein, humanLigandsPeptidesReceptors, KIR2DL2Receptors, KIR2DL3Killer-cell immunoglobulin-like receptorsMHC class INatural killer cellsPeptidePeptide selectivity

Identifiers

PMID25359276
PMCPMC4324016
OpenAlexW2035882024

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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.