Evidence map›Paper›PMID 20944005›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

PRDM1/Blimp-1 controls effector cytokine production in human NK cells.

Matthew A Smith, Michelle Maurin, Hyun Il Cho, Brian Becknell, Aharon G Freud, Jianhua Yu, Sheng Wei, Julie Djeu, Esteban Celis, Michael A Caligiuri and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
2.3field-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

63 citing papers in PubMed, 100 citations in OpenAlex.

  1. Role of PRDM1 in natural killer cells.Molecular biology reports · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
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  13. Article
  14. Article
  15. Article
  16. An autoimmune transcriptional circuit drives FOXP3Science translational medicine · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. Blimp-1 and c-Maf regulateWellcome open research · 2023
    Article

3 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

11 authors at 4 institutions in 1 country.

Matthew A SmithH. Lee Moffitt Cancer Center and Research Institute, University of South Florida, Tampa, FL 33612, USA.
Michelle Maurin
Hyun Il Cho
Brian Becknell
Aharon G Freud
Jianhua Yu
Sheng Wei
Julie Djeu
Esteban Celis
Michael A Caligiuri
Kenneth L Wright
Moffitt Cancer Center · USThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USThe Ohio State University · USUniversity of South Florida · US

Funding

PRDI-BF1 and histone methyltransferase in lymphomaR01CA114504 · NCI · H. LEE MOFFITT CANCER CTR &RES INST · PI WRIGHT, KENNETH LYNN · 2005 to 2009
$1.2M
NCI NIH HHS R01 CA114504
6 · The paper itself

Abstract

NK cells are major effectors of the innate immune response through cytolysis and bridge to the adaptive immune response through cytokine release. The mediators of activation are well studied; however, little is known about the mechanisms that restrain activation. In this report, we demonstrate that the transcriptional repressor PRDM1 (also known as Blimp-1 or PRDI-BF1) is a critical negative regulator of NK function. Three distinct PRDM1 isoforms are selectively induced in the CD56(dim) NK population in response to activation. PRDM1 coordinately suppresses the release of IFN-γ, TNF-α, and TNF-β through direct binding to multiple conserved regulatory regions. Ablation of PRDM1 expression leads to enhanced production of IFN-γ and TNF-α but does not alter cytotoxicity, whereas overexpression blocks cytokine production. PRDM1 response elements are defined at the IFNG and TNF loci. Collectively, these data demonstrate a key role for PRDM1 in the negative regulation of NK activation and position PRDM1 as a common regulator of the adaptive and innate immune response.

Indexed as

AnimalsBlotting, WesternChromatin ImmunoprecipitationCytokinesEnzyme-Linked Immunosorbent AssayGene Expression RegulationHumansKiller Cells, NaturalLymphocyte ActivationMiceMice, Inbred C57BLOligonucleotide Array Sequence AnalysisPositive Regulatory Domain I-Binding Factor 1Repressor ProteinsReverse Transcriptase Polymerase Chain ReactionCytokinesPositive Regulatory Domain I-Binding Factor 1PRDM1 protein, humanRepressor Proteins

Identifiers

PMID20944005
PMCPMC3864810
OpenAlexW2164455161

What OpenQuestion holds

Textmetadata
LicenceTDM
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.