Evidence map›Paper›PMID 25841627›Full record

ReviewSeminars in immunology2015

The transcriptional programs of iNKT cells.

Edy Y Kim, Lydia Lynch, Patrick J Brennan, Nadia R Cohen, Michael B Brenner

Abstract readReview
In one paragraph

Review in Seminars in immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

49 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Facts and Hopes of Chimeric Antigen Receptor-Redirected NK T Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Review
  5. Targeting orthotopic and metastatic pancreatic cancer with allogeneic stem cell-engineered mesothelin-redirected CAR-NKT cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Invariant natural killer T cells in lung diseases.Experimental & molecular medicine · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors.

Edy Y KimDivision of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, 15 Francis Street, Boston, MA 02115, United States; Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Smith Building, 5th Floor, 1 Jimmy Fund Way, Boston, MA 02115, United States. Electronic address: edyyongkim@gmail.com.
Lydia LynchDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Smith Building, 5th Floor, 1 Jimmy Fund Way, Boston, MA 02115, United States; Division of Endocrinology, Diabetes and Hypertension, Brigham and Women's Hospital, 221 Longwood Avenue, Boston, MA 02115, United States. Electronic address: llynch3@partners.org.
Patrick J BrennanDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Smith Building, 5th Floor, 1 Jimmy Fund Way, Boston, MA 02115, United States. Electronic address: pbrennan3@partners.org.
Nadia R CohenHoward Hughes Medical Institute, Wyss Institute for Biologically Inspired Engineering at Harvard University, 5(th) floor, 3 Blackfan Circle, Boston, MA 02115, United States. Electronic address: nadia.cohen@wyss.harvard.edu.
Michael B BrennerDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Smith Building, 5th Floor, 1 Jimmy Fund Way, Boston, MA 02115, United States. Electronic address: mbrenner@research.bwh.harvard.edu.

Funding

T LYMPOHOCYTE RECOGNITIONR01AI028973 · NIAID · DANA-FARBER CANCER INSTITUTE · PI BRENNER, MICHAEL B. · 1990 to 2014
$4.5M
Self and dietary lipid antigens for invariant natural killer T cellsK08AI102945 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BRENNAN, PATRICK JOSEPH · 2013 to 2016
$736k
NIAID NIH HHS AI102945NIAID NIH HHS K08 AI102945NIAID NIH HHS R01 AI028973
6 · The paper itself

Abstract

Invariant natural killer T (iNKT) cells are innate T cells that express a semi-invariant T cell receptor (TCR) and recognize lipid antigens presented by CD1d molecules. As part of innate immunity, iNKT cells rapidly produce large amounts of cytokines after activation and regulate the function of innate and adaptive immune cells in antimicrobial immunity, tumor rejection and inflammatory diseases. Global transcriptional profiling has advanced our understanding of all aspects of iNKT cell biology. In this review, we discuss transcriptional analyses of iNKT cell development, functional subsets of iNKT cells, and global comparisons of iNKT cells to other innate and adaptive immune cells. Global transcriptional analysis revealed that iNKT cells have a transcriptional profile distinct from NK cells and MHC-restricted T cells, both during thymic development and in the periphery. The transcription factors EGR2 and PLZF (and microRNA like miR-150) are key regulators of the iNKT cell transcriptome during development. PLZF is one of several factors that control the homing and maintenance of organ-specific iNKT cell populations. As in MHC-restricted T cells, specific transcription factors are characteristic of functional subsets of iNKT cells, such as the transcription factor T-bet in the NKT1 subset. Exciting future directions for global transcriptional analyses include iNKT cells in disease models, diverse NKT cells and human studies.

Indexed as

Transcription, GeneticAnimalsEarly Growth Response Protein 2HumansInflammationKruppel-Like Transcription FactorsMicroRNAsNatural Killer T-CellsTranscriptomeEarly Growth Response Protein 2Kruppel-Like Transcription FactorsMicroRNAsGlobal transcriptional profilingGlobal transcriptome profilingNKT cell developmentNKT cell subsetPLZF

Identifiers

PMID25841627
PMCPMC6322908

What OpenQuestion holds

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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.