Evidence map›Paper›PMID 30287480›Full record

ArticleThe Journal of experimental medicine2018

SOX4 controls invariant NKT cell differentiation by tuning TCR signaling.

Nidhi Malhotra, Yilin Qi, Nicholas A Spidale, Michela Frascoli, Bing Miu, Okhyun Cho, Katelyn Sylvia, Joonsoo Kang

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Invariant natural killer T cells in lung diseases.Experimental & molecular medicine · 2023
    Review
  11. Review
  12. Article
  13. Article
  14. A microRNA checkpoint for CaMolecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  15. Review
  16. Article
  17. Article
  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

8 authors at 1 institution in 1 country.

Nidhi MalhotraDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA.
Yilin QiDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA.
Nicholas A SpidaleDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA.ORCID 0000-0002-1568-4746
Michela FrascoliDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA.ORCID 0000-0003-1640-0415
Bing MiuDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA.ORCID 0000-0002-5670-917X
Okhyun ChoDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA.
Katelyn SylviaDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA.
Joonsoo KangDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA joonsoo.kang@umassmed.edu.ORCID 0000-0001-8419-7995
University of Massachusetts Chan Medical School · US

Funding

ETHICS COURSE SCIENTIST-PARTICIPANT PARTNERSHIPST15AI007551 · NIAID · FORDHAM UNIVERSITY · PI FISHER, CELIA B · 1998 to 2000
$77k
NIAID NIH HHS T15 AI007551
6 · The paper itself

Abstract

Natural killer T (NKT) cells expressing the invariant T cell receptor (iTCR) serve an essential function in clearance of certain pathogens and have been implicated in autoimmune and allergic diseases. Complex effector programs of these iNKT cells are wired in the thymus, and upon thymic egress, they can respond within hours of antigenic challenges, classifying iNKT cells as innate-like. It has been assumed that the successful rearrangement of the invariant iTCRα chain is the central event in the divergence of immature thymocytes to the NKT cell lineage, but molecular properties that render the iTCR signaling distinct to permit the T cell lineage diversification remain obscure. Here we show that the High Mobility Group (HMG) transcription factor (TF) SOX4 controls the production of iNKT cells by inducing MicroRNA-181 (

Indexed as

AnimalsCalcium SignalingGene Rearrangement, T-LymphocyteMiceMice, KnockoutMicroRNAsNatural Killer T-CellsReceptors, Antigen, T-CellSOXC Transcription FactorsThymocytesMicroRNAsmirn181 microRNA, mouseReceptors, Antigen, T-CellSox4 protein, mouseSOXC Transcription Factors

Identifiers

PMID30287480
PMCPMC6219734
OpenAlexW2895236957

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.