Evidence map›Paper›PMID 24747678›Full record

ArticleNature immunology2014

The transcription factor Zbtb32 controls the proliferative burst of virus-specific natural killer cells responding to infection.

Aimee M Beaulieu, Carolyn L Zawislak, Toshinori Nakayama, Joseph C Sun

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
7.3field-weighted citation impact, top 2% 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

95 citing papers in PubMed, 1 synthesis or guideline pooled it, 138 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Role of PRDM1 in natural killer cells.Molecular biology reports · 2026
    Review
  4. Article
  5. Therapeutic bacteria-trained NK cells confer long-term protection against cancer metastasis.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. IL-15 Priming Alters IFN-γ Regulation in Murine NK Cells.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Aimee M BeaulieuImmunology Program, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Carolyn L ZawislakImmunology Program, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Toshinori NakayamaDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Joseph C SunImmunology Program, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Memorial Sloan Kettering Cancer Center · USChiba University · JP

Funding

The natural killer cell response against mouse cytomegalovirus infectionR01AI100874 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI Joseph Chai-Yuen Sun · 2012 to 2026
$7.4M
IMMUNOLOGY RESEARCH TRAININGT32CA009149 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI RUDENSKY, ALEXANDER Y · 1985 to 2022
$4.0M
Natural killer cell responses against viral infectionR00AI085034 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI SUN, JOSEPH CHAI-YUEN · 2010 to 2011
$498k
MOLECULAR MECHANISMS OF YEAST TRANSCRIPTIONK04AI000874 · NIAID · INDIANA UNIVERSITY BLOOMINGTON · PI JAEHNING, JUDITH A. · 1988 to 1992
–
NCI NIH HHS T32 CA009149NIAID NIH HHS AI00874NIAID NIH HHS AI085034NIAID NIH HHS R00 AI085034NIAID NIH HHS R01 AI100874
6 · The paper itself

Abstract

Natural killer (NK) cells are innate lymphocytes that exhibit many features of adaptive immunity, including clonal proliferation and long-lived memory. Here we demonstrate that the BTB-ZF transcription factor Zbtb32 (also known as ROG, FAZF, TZFP and PLZP) was essential for the proliferative burst and protective capacity of virus-specific NK cells. Signals from proinflammatory cytokines were both necessary and sufficient to induce high expression of Zbtb32 in NK cells. Zbtb32 facilitated NK cell proliferation during infection by antagonizing the anti-proliferative factor Blimp-1 (Prdm1). Our data support a model in which Zbtb32 acts as a cellular 'hub' through which proinflammatory signals instruct a 'proliferation-permissive' state in NK cells, thereby allowing their prolific expansion in response to viral infection.

Indexed as

Adaptive ImmunityAnimalsCell ProliferationCell SurvivalCytokinesHerpesviridae InfectionsImmunologic MemoryInflammationKiller Cells, NaturalLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMuromegalovirusPositive Regulatory Domain I-Binding Factor 1Repressor ProteinsCytokinesPositive Regulatory Domain I-Binding Factor 1Prdm1 protein, mouseRepressor ProteinsRog protein, mouseTranscription Factors

Identifiers

PMID24747678
PMCPMC4404304
OpenAlexW1975717760

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.