Evidence map›Paper›PMID 25101089›Full record

ArticleFrontiers in immunology2014

Adaptations of Natural Killer Cells to Self-MHC Class I.

Stéphanie Bessoles, Camille Grandclément, Elisenda Alari-Pahissa, Jasmine Gehrig, Beena Jeevan-Raj, Werner Held

Abstract read
In one paragraph

Article in Frontiers in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. Article
  13. Computational KIR copy number discovery reveals interaction between inhibitory receptor burden and survival.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2019
    Article
  14. Review
  15. Article
  16. Dysfunctional Natural Killer Cells in the Aftermath of Cancer Surgery.International journal of molecular sciences · 2017
    Review
  17. Review
  18. Regulatory circuits of T cell function in cancer.Nature reviews. Immunology · 2016
    Review
  19. Article
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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

6 authors.

Stéphanie BessolesDepartment of Oncology, Ludwig Center for Cancer Research, University of Lausanne , Lausanne , Switzerland.
Camille GrandclémentDepartment of Oncology, Ludwig Center for Cancer Research, University of Lausanne , Lausanne , Switzerland.
Elisenda Alari-PahissaDepartment of Oncology, Ludwig Center for Cancer Research, University of Lausanne , Lausanne , Switzerland.
Jasmine GehrigDepartment of Oncology, Ludwig Center for Cancer Research, University of Lausanne , Lausanne , Switzerland.
Beena Jeevan-RajDepartment of Oncology, Ludwig Center for Cancer Research, University of Lausanne , Lausanne , Switzerland.
Werner HeldDepartment of Oncology, Ludwig Center for Cancer Research, University of Lausanne , Lausanne , Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural Killer (NK) cells use germ line encoded receptors to detect diseased host cells. Despite the invariant recognition structures, NK cells have a significant ability to adapt to their surroundings, such as the presence or absence of MHC class I molecules. It has been assumed that this adaptation occurs during NK cell development, but recent findings show that mature NK cells can also adapt to the presence or absence of MHC class I molecules. Here, we summarize how NK cells adjust to changes in the expression of MHC class I molecules. We propose an extension of existing models, in which MHC class I recognition during NK cell development sequentially instructs and maintains NK cell function. The elucidation of the molecular basis of the two effects may identify ways to improve the fitness of NK cells and to prevent the loss of NK cell function due to persistent alterations in their environment.

Indexed as

educationlicensingLy49 receptorsMHC class INK cells

Identifiers

PMID25101089
PMCPMC4106420

What OpenQuestion holds

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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.