Evidence map›Paper›PMID 22962434›Full record

ArticleInternational immunology2012

Identification of human NK cells that are deficient for signaling adaptor FcRγ and specialized for antibody-dependent immune functions.

Ilwoong Hwang, Tianxiang Zhang, Jeannine M Scott, Ae Ra Kim, Taehyung Lee, Tejaswi Kakarla, Ahrom Kim, John B Sunwoo, Sungjin Kim

Open access · bronzeAbstract read
In one paragraph

Article in International immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

119 citing papers in PubMed, 167 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. HLA-E-Directed Accumulation of KIRInternational journal of molecular sciences · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Editor's pick: Indapta Therapeutics.Nature biotechnology · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Nutrient transporter pattern in CD56Frontiers in immunology · 2024
    Article

59 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

9 authors at 2 institutions in 1 country.

Ilwoong HwangDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA. kimsj@msu.edu
Tianxiang Zhang
Jeannine M Scott
Ae Ra Kim
Taehyung Lee
Tejaswi Kakarla
Ahrom Kim
John B Sunwoo
Sungjin Kim
Michigan State University · USStanford University · US

Funding

Natural killer cell genetics and cancerR21CA149476 · NCI · MICHIGAN STATE UNIVERSITY · PI KIM, SUNGJIN · 2010 to 2011
$359k
NCI NIH HHS 5R21CA149476NCI NIH HHS R21 CA149476
6 · The paper itself

Abstract

NK cells respond to tumor and virus-infected cells directly through several activation receptors, including natural cytotoxicity receptors, or indirectly through the activating Fc receptor CD16 for antibody-coated cells. Triggering of NK-cell effector functions through these receptors depends on physically associated transmembrane signaling adaptors, such as FcRγ (also known as FcεRIγ) and CD3ζ, both of which have been traditionally believed to be expressed by all mature NK cells. However, we have identified a distinct subset of human NK cells that are deficient for FcRγ expression but express normal levels of CD3ζ. FcRγ-deficient NK cells were readily detectable in about one-third of the healthy individuals examined. The deficiency was confined to the CD56(dim) population and was due to low FcRγ mRNA. FcRγ-deficient NK cells displayed dramatically reduced expression of the natural cytotoxicity receptors NKp46 and NKp30 but still expressed substantial levels of CD16. Compared to FcRγ-expressing NK cells, FcRγ-deficient NK cells showed poor direct reactivity toward tumor targets as measured by cytokine production and degranulation. Unexpectedly, however, FcRγ-deficient NK cells exhibited significantly more robust responsiveness upon stimulation through CD16, particularly for cytokine production, compared to FcRγ-expressing NK cells. Thus, our study reveals FcRγ-deficient NK cells as a novel subset of human NK cells that have remarkably potent responses toward antibody-coated targets. These findings also illustrate a differential contribution of FcRγ and CD3ζ for the expression and functional activity of their associated receptors.

Indexed as

AntibodiesAntigens, NeoplasmCD3 ComplexCells, CulturedCytokinesHumansImmunophenotypingKiller Cells, NaturalLymphocyte SubsetsNatural Cytotoxicity Triggering Receptor 1Natural Cytotoxicity Triggering Receptor 3NeoplasmsReceptor Cross-TalkReceptors, IgGSignal TransductionAntibodiesAntigens, NeoplasmCD3 ComplexCytokinesNatural Cytotoxicity Triggering Receptor 1Natural Cytotoxicity Triggering Receptor 3Receptors, IgG

Identifiers

PMID22962434
PMCPMC3621379
OpenAlexW2124872606

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.