Evidence map›Paper›PMID 22772778›Full record

ArticleImmunogenetics2012

Quantity of HLA-C surface expression and licensing of KIR2DL+ natural killer cells.

Hojjatollah Nozad Charoudeh, Laurent Schmied, Asensio Gonzalez, Grzegorz Terszowski, Karol Czaja, Karin Schmitter, Laura Infanti, Andreas Buser, Martin Stern

Abstract read
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In one paragraph

Article in Immunogenetics, 2012. 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
1.5field-weighted citation impact, top 19% 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, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Single Nucleotide Polymorphism inFrontiers in immunology · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Beyond Viral Neutralization.AIDS research and human retroviruses · 2017
    Review
  9. Recipient HLA-C Haplotypes and microRNA 148a/b Binding Sites Have No Impact on Allogeneic Hematopoietic Cell Transplantation Outcomes.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2017
    Article
  10. Article
  11. Article
  12. Cognate HLA absence in trans diminishes human NK cell education.The Journal of clinical investigation · 2016
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  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

9 authors at 2 institutions in 2 countries.

Hojjatollah Nozad CharoudehImmunotherapy Laboratory, Department of Biomedicine, University Hospital Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Laurent Schmied
Asensio Gonzalez
Grzegorz Terszowski
Karol Czaja
Karin Schmitter
Laura Infanti
Andreas Buser
Martin Stern
Department of Biomedicine Basel · CHUniversity Hospital of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells require interaction of inhibitory surface receptors with human leukocyte antigen (HLA) ligands during development to acquire functional competence in a process termed "licensing." The quantity of HLA required for this process is unknown. Two polymorphisms affecting HLA-C surface expression (rs9264942 and rs67384697) have recently been identified, and shown to influence progression of HIV infection. We typed a cohort of healthy donors for the two HLA-C-related polymorphisms, KIR2DL1 and KIR2DL3, and their respective HLA-C ligands and analyzed how HLA ligands influenced licensing status of killer cell immunoglobulin-like receptor (KIR)+ NK cells in terms of degranulation and cytokine production in response to HLA-deficient target cells. The presence of respective HLA class I ligands increased the function of KIR2DL1+ and KIR2DL3+ NK cells in a dose-dependent manner. In contrast, neither of the HLA-C-related polymorphisms nor the quantity of cell surface HLA-C had any significant effect on NK cell function. Interestingly, HLA-Cw7-an HLA-C allele with low surface expression-licensed KIR2DL3+ NK cells more strongly than any other KIR2DL3 ligand. The quantity of cell surface HLA-C does not appear to influence licensing of NK cells, and the HLA-C-related polymorphisms presumably influence HIV progression through factors unrelated to NK cell education.

Indexed as

DNAGenotypeHIV InfectionsHLA-C AntigensHumansKiller Cells, NaturalLeukocytesLigandsPolymerase Chain ReactionPolymorphism, GeneticReceptors, KIRReceptors, KIR2DL1Receptors, KIR2DL2Receptors, KIR2DL3DNAHLA-C AntigensLigandsReceptors, KIRReceptors, KIR2DL1Receptors, KIR2DL2Receptors, KIR2DL3

Identifiers

PMID22772778
OpenAlexW2044862851

What OpenQuestion holds

Textmetadata
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.