Evidence map›Paper›PMID 28561023›Full record

ArticleNature communications2017

Expression of CD226 is associated to but not required for NK cell education.

Arnika K Wagner, Nadir Kadri, Johanna Snäll, Petter Brodin, Susan Gilfillan, Marco Colonna, Günter Bernhardt, Petter Höglund, Klas Kärre, Benedict J Chambers

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
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  13. Identification of aceNKPs, a committed common progenitor population of the ILC1 and NK cell continuum.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Licensing Natural Killers for Antiviral Immunity.Pathogens (Basel, Switzerland) · 2021
    Review
  19. Article
  20. 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

10 authors at 4 institutions in 3 countries.

Arnika K WagnerDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Nobels väg 16, 17177 Stockholm, Sweden.
Nadir KadriDepartment of Medicine Huddinge, Center for Hematology and Regenerative Medicine, Karolinska Institutet, Hälsovägen 7, 14157 Huddinge, Sweden.
Johanna SnällDepartment of Medicine Huddinge, Center for Infectious Medicine, Karolinska Institutet, F59, 14186 Stockholm, Sweden.
Petter BrodinScience for Life Laboratory, Department of Medicine Solna, Karolinska Institutet, and Unit of Infectious Diseases, Karolinska University Hospital, 17176 Stockholm, Sweden.
Susan GilfillanDepartment of Pathology and Immunology, Campus Box 8118, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, Missouri 63110, USA.
Marco ColonnaDepartment of Pathology and Immunology, Campus Box 8118, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, Missouri 63110, USA.
Günter BernhardtInstitute of Immunology, Building 11, Hannover Medical School, Carl Neuberg Straße1, 30625 Hannover, Germany.
Petter HöglundDepartment of Medicine Huddinge, Center for Hematology and Regenerative Medicine, Karolinska Institutet, Hälsovägen 7, 14157 Huddinge, Sweden.
Klas KärreDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Nobels väg 16, 17177 Stockholm, Sweden.
Benedict J ChambersDepartment of Medicine Huddinge, Center for Infectious Medicine, Karolinska Institutet, F59, 14186 Stockholm, Sweden.
Karolinska Institutet · SEWashington University in St. Louis · USMedizinische Hochschule Hannover · DEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNAX accessory molecule-1 (DNAM-1, also known as CD226) is an activating receptor expressed on subsets of natural killer (NK) and T cells, interacts with its ligands CD155 or CD112, and has co-varied expression with inhibitory receptors. Since inhibitory receptors control NK-cell activation and are necessary for MHC-I-dependent education, we investigated whether DNAM-1 expression is also involved in NK-cell education. Here we show an MHC-I-dependent correlation between DNAM-1 expression and NK-cell education, and an association between DNAM-1 and NKG2A that occurs even in MHC class I deficient mice. DNAM-1 is expressed early during NK-cell development, precedes the expression of MHC-I-specific inhibitory receptors, and is modulated in an education-dependent fashion. Cd226

Indexed as

AnimalsAntigens, Differentiation, T-Lymphocytebeta 2-MicroglobulinCells, CulturedFemaleHistocompatibility Antigens Class IKiller Cells, NaturalLymphocyte ActivationMaleMiceMice, Inbred C57BLMice, KnockoutNectinsNeoplasmsNK Cell Lectin-Like Receptor Subfamily CReceptors, VirusAntigens, Differentiation, T-Lymphocytebeta 2-MicroglobulinHistocompatibility Antigens Class INectinsNK Cell Lectin-Like Receptor Subfamily Cpoliovirus receptorReceptors, VirusT Lineage-Specific Activation Antigen 1

Identifiers

PMID28561023
PMCPMC5460037
OpenAlexW2620343734

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.