Evidence map›Paper›PMID 23382564›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

A peptide antagonist disrupts NK cell inhibitory synapse formation.

Gwenoline Borhis, Parvin S Ahmed, Bérénice Mbiribindi, Mohammed M Naiyer, Daniel M Davis, Marco A Purbhoo, Salim I Khakoo

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Infection and immunity · 2026
    Review
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  16. Synergistic inhibition of natural killer cells by the nonsignaling molecule CD94.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  17. Immunogenetics of HIV disease.Immunological reviews · 2013
    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

7 authors at 2 institutions in 1 country.

Gwenoline BorhisDivision of Medicine, Imperial College London, London SW7 2AZ, United Kingdom.
Parvin S Ahmed
Bérénice Mbiribindi
Mohammed M Naiyer
Daniel M Davis
Marco A Purbhoo
Salim I Khakoo
Imperial College London · GBUniversity of Southampton · GB

Funding

Medical Research Council G0500563Medical Research Council G1001044Medical Research Council G1001738Wellcome Trust 076991
6 · The paper itself

Abstract

Productive engagement of MHC class I by inhibitory NK cell receptors depends on the peptide bound by the MHC class I molecule. Peptide:MHC complexes that bind weakly to killer cell Ig-like receptors (KIRs) can antagonize the inhibition mediated by high-affinity peptide:MHC complexes and cause NK cell activation. We show that low-affinity peptide:MHC complexes stall inhibitory signaling at the step of Src homology protein tyrosine phosphatase 1 recruitment and do not go on to form the KIR microclusters induced by high-affinity peptide:MHC, which are associated with Vav dephosphorylation and downstream signaling. Furthermore, the low-affinity peptide:MHC complexes prevented the formation of KIR microclusters by high-affinity peptide:MHC. Thus, peptide antagonism of NK cells is an active phenomenon of inhibitory synapse disruption.

Indexed as

Cell LineKiller Cells, NaturalMutationPeptidesPhenylalanineProtein BindingReceptors, KIR2DL3Signal TransductionSynapsesKIR2DL3 protein, humanPeptidesPhenylalanineReceptors, KIR2DL3

Identifiers

PMID23382564
PMCPMC3672982
OpenAlexW2129069571

What OpenQuestion holds

Textmetadata
LicenceTDM
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.