Evidence map›Paper›PMID 17296789›Full record

ArticleThe Journal of experimental medicine2007

Expression of the transcription factor cKrox in peripheral CD8 T cells reveals substantial postthymic plasticity in CD4-CD8 lineage differentiation.

S Rhiannon Jenkinson, Andrew M Intlekofer, Guangping Sun, Lionel Feigenbaum, Steven L Reiner, Rémy Bosselut

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 73 citations in OpenAlex.

  1. CD4Science (New York, N.Y.) · 2026
    Article
  2. Cytotoxic CD4Signal transduction and targeted therapy · 2026
    Review
  3. Transcriptional network dynamics in early T cell development.The Journal of experimental medicine · 2024
    Review
  4. Pathways and mechanisms of CD4Trends in immunology · 2024
    Review
  5. A conserved element in the first intron ofFrontiers in immunology · 2024
    Article
  6. Zfp281 and Zfp148 control CD4Science immunology · 2023
    Article
  7. Generation of Retrogenic Mice to Investigate T Cell Development.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. A STAT3-dependent transcriptional circuitry inhibits cytotoxic gene expression in T cells.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  14. Article
  15. Review
  16. Review
  17. Review
  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

6 authors at 3 institutions in 1 country.

S Rhiannon JenkinsonLaboratory of Immune Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Andrew M Intlekofer
Guangping Sun
Lionel Feigenbaum
Steven L Reiner
Rémy Bosselut
National Institutes of Health · USCancer Research Institute · USScience Applications International Corporation (United States) · US

Funding

Genetic Analysis of T-cell DifferentiationZ01BC010671 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BOSSELUT, REMY · 2005 to 2008
$2.9M
GENE SILENCING IN THE IMMUNE RESPONSE TO PARASITESR01AI053827 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI REINER, STEVEN L · 2003 to 2007
$1.9M
Intramural NIH HHSNIAID NIH HHS AI053827NIAID NIH HHS R01 AI053827
6 · The paper itself

Abstract

Most T cells belong to either of two lineages defined by the mutually exclusive expression of CD4 and CD8 coreceptors: CD4 T cells are major histocompatibility complex (MHC) II restricted and have helper function, whereas CD8 T cells are MHC I restricted and have cytotoxic function. The divergence between these two lineages occurs during intrathymic selection and is thought to be irreversible in mature T cells. It is, however, unclear whether the CD4-CD8 differentiation of postthymic T cells retains some level of plasticity or is stably maintained by mechanisms distinct from those that set lineage choice in the thymus. To address this issue, we examined if coreceptor or effector gene expression in mature CD8 T cells remains sensitive to the zinc finger transcription factor cKrox, which promotes CD4 and inhibits CD8 differentiation when expressed in thymocytes. We show that cKrox transduction into CD8 T cells inhibits their expression of CD8 and cytotoxic effector genes and impairs their cytotoxic activity, and that it promotes expression of helper-specific genes, although not of CD4 itself. These observations reveal a persistent degree of plasticity in CD4-CD8 differentiation in mature T cells.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8 AntigensCD8-Positive T-LymphocytesCell DifferentiationCell LineageCells, CulturedDNA-Binding ProteinsGene Expression RegulationMiceMice, Inbred C57BLRetroviridaeTranscription FactorsTransduction, GeneticCD8 AntigensDNA-Binding ProteinsTranscription FactorsZbtb7a protein, mouse

Identifiers

PMID17296789
PMCPMC2118724
OpenAlexW2105830996

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.