Evidence map›Paper›PMID 24079744›Full record

ArticleExperimental dermatology2013

Deletion of the activating NKG2C receptor and a functional polymorphism in its ligand HLA-E in psoriasis susceptibility.

Xue Zeng, Haoyan Chen, Rashmi Gupta, Oscar Paz-Altschul, Anne M Bowcock, Wilson Liao

Open access · greenAbstract readLetter
In one paragraph

Article in Experimental dermatology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Role of Innate Immune Cells in Psoriasis.International journal of molecular sciences · 2020
    Review
  11. Dimorphism of HLA-E and its Disease Association.International journal of molecular sciences · 2019
    Review
  12. Article
  13. Article
  14. Tumor necrosis factor superfamily in innate immunity and inflammation.Cold Spring Harbor perspectives in biology · 2014
    Review
  15. Article
  16. Review
  17. Review
  18. HLA-E: a novel player for histocompatibility.Journal of immunology research · 2014
    Review
  19. Article
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 at 3 institutions in 3 countries.

Xue ZengDepartment of Dermatology, University of California San Francisco, San Francisco, CA, USA; Department of Dermatology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Haoyan Chen
Rashmi Gupta
Oscar Paz-Altschul
Anne M Bowcock
Wilson Liao
University of California, San Francisco · USChinese Academy of Medical Sciences & Peking Union Medical College · CNImperial College London · GB

Funding

Genome-Wide SNP Association in PsoriasisR01AR050266 · NIAMS · WASHINGTON UNIVERSITY · PI BOWCOCK, ANNE MARY · 2007 to 2016
$5.7M
Identification of Causal Variants in PsoriasisR01AR065174 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LIAO, WILSON · 2013 to 2016
$1.8M
Genetic Analysis of the TNF Pathway in PsoriasisK08AR057763 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LIAO, WILSON · 2010 to 2014
$599k
NIAMS NIH HHS 5K08AR057763NIAMS NIH HHS AR050266NIAMS NIH HHS K08 AR057763NIAMS NIH HHS R01 AR050266NIAMS NIH HHS R01 AR065174
6 · The paper itself

Abstract

Psoriasis is an inflammatory, immune-mediated disease of the skin. Several studies have suggested that natural killer (NK) cells and their receptors may be important for its pathogenesis. Here, we examined whether deletion of the activating natural killer receptor gene NKG2C, which has a frequency of 20% in the European population, was associated with psoriasis susceptibility. The NKG2C deletion and a functional polymorphism in its ligand HLA-E were genotyped in a Caucasian cohort of 611 psoriasis cases and 493 controls. We found that the NKG2C deletion was significantly increased in cases compared with controls [0.258 vs 0.200, P = 0.0012, OR = 1.43 (1.15-1.79)]. The low-expressing HLA-E*01:01 allele was associated with psoriasis (P = 0.0018), although this association was dependent on HLA-C. Our findings support a potential immunoregulatory role for NK cells in psoriasis and suggest the importance of future studies to investigate the contribution of NK cells and their regulatory receptors to the pathogenesis of psoriasis.

Indexed as

Genetic Predisposition to DiseasePolymorphism, GeneticAllelesCase-Control StudiesCohort StudiesGene DeletionGenetic VariationGenotypeHistocompatibility Antigens Class IHLA-E AntigensHumansInflammationKiller Cells, NaturalLigandsNK Cell Lectin-Like Receptor Subfamily CPolymerase Chain ReactionHistocompatibility Antigens Class IHLA-E AntigensKLRC2 protein, humanLigandsNK Cell Lectin-Like Receptor Subfamily CHLA-EKLRC2natural killerNKG2Cpsoriasis

Identifiers

PMID24079744
PMCPMC3813441
OpenAlexW2018961628

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.