Evidence map›Paper›PMID 29452898›Full record

ReviewCurrent opinion in immunology2018

Transcriptional and epigenetic regulation of innate-like T lymphocyte development.

Mihalis Verykokakis, Barbara L Kee

Abstract readReview
In one paragraph

Review in Current opinion in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Key Functions of the Transcription Factor BCL6 During T-Cell Differentiation.Advances in experimental medicine and biology · 2024
    Review
  5. TET proteins regulateFrontiers in immunology · 2024
    Article
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  8. Article
  9. Article
  10. Review
  11. Article
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  13. Article
  14. Review
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  17. Review
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

2 authors.

Mihalis VerykokakisBiomedical Sciences Research Center "Alexander Fleming", 34 Fleming St, 16672 Vari, Greece. Electronic address: verykokakis@fleming.gr.
Barbara L KeeDepartment of Pathology and Committee on Immunology, The University of Chicago, Chicago, IL 60657, USA. Electronic address: bkee@bsd.uchicago.edu.

Funding

Mechanisms of E protein transcription factor-dependent iNKT cell expansion and differentiationR01AI123396 · NIAID · UNIVERSITY OF CHICAGO · PI KEE, BARBARA L. · 2017 to 2021
$2.0M
NIAID NIH HHS R01 AI123396
6 · The paper itself

Abstract

Invariant Natural Killer T (iNKT) cells are a heterogeneous innate T cell population that recognizes lipid antigens. Despite the monospecific nature of their T cell receptor, iNKT cells differentiate into stable sublineages during thymic development, before foreign antigen encounter. How iNKT cell subsets acquire and maintain their functional programs is a central question in innate lymphocyte biology. Global transcriptional and epigenetic profiling of iNKT subsets has provided insights into the internal wiring of these subsets that defines their identity. Comparison of the iNKT transcriptional programs with those of other adaptive and innate lymphocyte lineages revealed common core regulatory circuits that may dictate effector functions. In this review, we summarize recent advances on the molecular mechanisms involved in iNKT cell development.

Indexed as

Epigenesis, GeneticImmunity, InnateTranscription, GeneticAnimalsCell DifferentiationGene Expression Regulation, DevelopmentalHumansLymphopoiesisNatural Killer T-CellsT-Lymphocyte Subsets

Identifiers

PMID29452898
PMCPMC5943139

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.