Evidence map›Paper›PMID 22057288›Full record

ArticleNature immunology2011

Repression of the DNA-binding inhibitor Id3 by Blimp-1 limits the formation of memory CD8+ T cells.

Yun Ji, Zoltan Pos, Mahadev Rao, Christopher A Klebanoff, Zhiya Yu, Madhusudhanan Sukumar, Robert N Reger, Douglas C Palmer, Zachary A Borman, Pawel Muranski and 5 more

Abstract read
In one paragraph

Article in Nature immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers.

0numbers the graph read from it
0cells of the map it votes in
134citing papers in PubMed
6.8field-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

134 citing papers in PubMed, 197 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. HEB Restrains Effector Gene Expression during Early CD8Molecular and cellular biology · 2025
    Article
  9. Article
  10. Article
  11. LIM-domain-only 4 (LMO4) enhances CD8Signal transduction and targeted therapy · 2024
    Article
  12. Review
  13. CD8+ Tissue-Resident Memory T Cells: Versatile Guardians of the Tissue.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Article
  14. Article
  15. Transcriptional rewiring in CD8Frontiers in immunology · 2024
    Review
  16. Antigen exposure reshapes chromatin architecture in central memory CD8Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Article
  18. Stem-like exhausted and memory CD8Nature reviews. Cancer · 2023
    Review
  19. The role of CD4MedComm · 2023
    Review
  20. Article

74 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

15 authors at 4 institutions in 1 country.

Yun JiCenter for Cancer Research, National Cancer Institute, US National Institutes of Health, Bethesda, Maryland, USA.
Zoltan Pos
Mahadev Rao
Christopher A Klebanoff
Zhiya Yu
Madhusudhanan Sukumar
Robert N Reger
Douglas C Palmer
Zachary A Borman
Pawel Muranski
Ena Wang
David S Schrump
Francesco M Marincola
Nicholas P Restifo
Luca Gattinoni
National Institutes of Health · USCenter for Cancer Research · USNational Cancer Institute · USNational Institutes of Health Clinical Center · US

Funding

Building on the success of the adoptive immunotherapy of cancerZIABC010763 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ROSENBERG, STEVEN · 2009 to 2020
$25.0M
Immunogenetic Study of Infectious Diseases and CancerZIACL002118 · CLC · CLINICAL CENTER · PI MARINCOLA, FRANCESCO M · 2009 to 2012
$0k
Intramural NIH HHS ZIA BC010763
6 · The paper itself

Abstract

The transcriptional repressor Blimp-1 promotes the differentiation of CD8(+) T cells into short-lived effector cells (SLECs) that express the lectin-like receptor KLRG-1, but how it operates remains poorly defined. Here we show that Blimp-1 bound to and repressed the promoter of the gene encoding the DNA-binding inhibitor Id3 in SLECs. Repression of Id3 by Blimp-1 was dispensable for SLEC development but limited the ability of SLECs to persist as memory cells. Enforced expression of Id3 was sufficient to restore SLEC survival and enhanced recall responses. Id3 function was mediated in part through inhibition of the transcriptional activity of E2A and induction of genes regulating genome stability. Our findings identify the Blimp-1-Id3-E2A axis as a key molecular switch that determines whether effector CD8(+) T cells are programmed to die or enter the memory pool.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCD8-Positive T-LymphocytesCell DifferentiationCell Line, TumorDNA RepairDNA ReplicationFemaleGene Expression ProfilingGene Expression RegulationImmunologic MemoryInhibitor of Differentiation Protein 2Inhibitor of Differentiation ProteinsLectins, C-TypeMiceMice, 129 StrainBasic Helix-Loop-Helix ProteinsIdb2 protein, mouseIdb3 protein, mouseInhibitor of Differentiation Protein 2Inhibitor of Differentiation ProteinsKlrg1 protein, mouseLectins, C-TypePositive Regulatory Domain I-Binding Factor 1Prdm1 protein, mouseReceptors, ImmunologicTcf3 protein, mouseTranscription Factors

Identifiers

PMID22057288
PMCPMC3226770
OpenAlexW2085887337

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.