Evidence map›Paper›PMID 16249390›Full record

ArticleBlood2006

Regulation of ITAM-positive receptors: role of IL-12 and IL-18.

John R Ortaldo, Robin Winkler-Pickett, Jon Wigginton, Meagan Horner, Earl W Bere, Anna T Mason, Narayan Bhat, James Cherry, Michael Sanford, Deborah L Hodge and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-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

24 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Review
  3. Natural killer cells in the lung: potential role in asthma and virus-induced exacerbation?European respiratory review : an official journal of the European Respiratory Society · 2023
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. MicroRNA function in NK-cell biology.Immunological reviews · 2013
    Review
  15. Mechanisms of NK cell activation: CD4(+) T cells enter the scene.Cellular and molecular life sciences : CMLS · 2011
    Review
  16. PRDM1/Blimp-1 controls effector cytokine production in human NK cells.Journal of immunology (Baltimore, Md. : 1950) · 2010
    Article
  17. Article
  18. Article
  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

11 authors at 1 institution in 1 country.

John R OrtaldoLaboratory of Experimental Immunology and Pediatric Oncology Branch, National Cancer Institute-Center for Cancer Research, Frederick, MD 21702-1201, USA.
Robin Winkler-Pickett
Jon Wigginton
Meagan Horner
Earl W Bere
Anna T Mason
Narayan Bhat
James Cherry
Michael Sanford
Deborah L Hodge
Howard A Young
Science Applications International Corporation (United States) · US

Funding

Control of Cytokine Gene Expression in LymphoidMyeloid CellsZIABC009283 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI YOUNG, HOWARD · 2009 to 2024
$22.7M
CONTROL OF HUMAN INTERFERON GAMMA GENE EXPRESSIONZ01BC009283 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI YOUNG, HOWARD A · 1996 to 2008
$2.6M
Intramural NIH HHS
6 · The paper itself

Abstract

Our previous studies have identified mechanisms by which cytokine production, blocked by Ly49G2 receptor cross-linking, can be overridden. In this study we analyzed the regulation of other ITAM-positive receptor signaling on NK, NKT, and T cells and characterized the biochemical pathways involved in this signaling. Our studies demonstrate that cross-linking of NKG2D and NK1.1 results in a synergistic NK IFN-gamma response when combined with IL-12 or IL-18. Examination of NKT- and T-cell responses demonstrated that cross-linking of NKG2D and CD3 resulted in potent synergy when combined with IL-12 and, to a lesser degree, with IL-18. We have now found that both the p38 MAP kinase and the ERK-dependent signal transduction pathways are required for the synergistic response. Further mechanistic examination of the synergy indicated a potent up-regulation of total IFN-gamma mRNA in the nuclear and the cytoplasmic compartment, but mRNA half-life was not affected. Fifteen minutes of IL-12 pretreatment was sufficient to result in maximal synergistic activation, indicating that the response of the cells to the IL-12 signal was rapid and immediate. Thus, our data demonstrate that multiple convergent signals maximize the innate immune response by triggering complementary biochemical signaling pathways.

Indexed as

Amino Acid SubstitutionAnimalsAntigens, LyCell LineCytokinesFlow CytometryInterferon-gammaInterleukin-12Interleukin-18Killer Cells, NaturalLectins, C-TypeMiceMice, Inbred BALB CNK Cell Lectin-Like Receptor Subfamily KPolymerase Chain ReactionReceptors, ImmunologicAntigens, LyCytokinesInterferon-gammaInterleukin-12Interleukin-18Klrk1 protein, mouseLectins, C-TypeNK Cell Lectin-Like Receptor Subfamily KReceptors, ImmunologicReceptors, Natural Killer CellReceptors, NK Cell Lectin-LikeRibonucleases

Identifiers

PMID16249390
PMCPMC1895416
OpenAlexW2114084633

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.