Evidence map›Paper›PMID 17360655›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Identification, activation, and selective in vivo ablation of mouse NK cells via NKp46.

Thierry Walzer, Mathieu Bléry, Julie Chaix, Nicolas Fuseri, Lionel Chasson, Scott H Robbins, Sébastien Jaeger, Pascale André, Laurent Gauthier, Laurent Daniel and 8 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 234 papers.

0numbers the graph read from it
0cells of the map it votes in
234citing papers in PubMed
12.4field-weighted citation impact, top 1% 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

234 citing papers in PubMed, 452 citations in OpenAlex.

  1. Article
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  6. OMIP-111: Immune-Profiling of T Helper 1 (Th1), Th2, and Th17 Signatures in Murine Splenocytes by Targeting Intracellular Cytokines.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2025
    Article
  7. Article
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  13. NK-cell receptor modulation in viral infections.Clinical and experimental immunology · 2024
    Review
  14. Article
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  16. Review
  17. Article
  18. Review
  19. Article
  20. Review

174 more citing papers are in PubMed but not listed here.

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

18 authors at 5 institutions in 2 countries.

Thierry WalzerCentre d'Immunologie de Marseille-Luminy, Université de la Méditerranée, 13288 Marseille, France. walzer@ciml.univ-mrs.fr
Mathieu Bléry
Julie Chaix
Nicolas Fuseri
Lionel Chasson
Scott H Robbins
Sébastien Jaeger
Pascale André
Laurent Gauthier
Laurent Daniel
Karine Chemin
Yannis Morel
Marc Dalod
Jean Imbert
Michel Pierres
Alessandro Moretta
François Romagné
Eric Vivier
Innate Pharma (France) · FRCentre d’Immunologie de Marseille-Luminy · FRInserm · FRAssistance Publique Hôpitaux de Marseille · FRUniversity of Genoa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells contribute to a variety of innate immune responses to viruses, tumors and allogeneic cells. However, our understanding of NK cell biology is severely limited by the lack of consensus phenotypic definition of these cells across species, by the lack of specific marker to visualize them in situ, and by the lack of a genetic model where NK cells may be selectively ablated. NKp46/CD335 is an Ig-like superfamily cell surface receptor involved in human NK cell activation. In addition to human, we show here that NKp46 is expressed by NK cells in all mouse strains analyzed, as well as in three common monkey species, prompting a unifying phenotypic definition of NK cells across species based on NKp46 cell surface expression. Mouse NKp46 triggers NK cell effector function and allows the detection of NK cells in situ. NKp46 expression parallels cell engagement into NK differentiation programs because it is detected on all NK cells from the immature CD122(+)NK1.1(+)DX5(-) stage and on a minute fraction of NK-like T cells, but not on CD1d-restricted NKT cells. Moreover, human NKp46 promoter drives NK cell selective expression both in vitro and in vivo. Using NKp46 promoter, we generated transgenic mice expressing EGFP and the diphtheria toxin (DT) receptor in NK cells. DT injection in these mice leads to a complete and selective NK cell ablation. This model paves a way for the in vivo characterization and preclinical assessment of NK cell biological function.

Indexed as

AnimalsAntigens, LyCell DifferentiationDiphtheria ToxinFlow CytometryGene Expression RegulationGreen Fluorescent ProteinsHaplorhiniImmunophenotypingKiller Cells, NaturalMembrane GlycoproteinsMiceMice, TransgenicMicroscopy, FluorescenceNatural Cytotoxicity Triggering Receptor 1Promoter Regions, GeneticAntigens, LyDiphtheria Toxinenhanced green fluorescent proteinGreen Fluorescent ProteinsMembrane GlycoproteinsNatural Cytotoxicity Triggering Receptor 1Ncr1 protein, mouseReceptors, Immunologic

Identifiers

PMID17360655
PMCPMC1805551
OpenAlexW2036806857

What OpenQuestion holds

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Registered trials

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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.