Evidence map›Paper›PMID 28576977›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Monoclonal Invariant NKT (iNKT) Cell Mice Reveal a Role for Both Tissue of Origin and the TCR in Development of iNKT Functional Subsets.

Eleanor Clancy-Thompson, Gui Zhen Chen, Paul M Tyler, Mariah M Servos, Marta Barisa, Patrick J Brennan, Hidde L Ploegh, Stephanie K Dougan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Development of αβ T Cells with Innate Functions.Advances in experimental medicine and biology · 2022
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  10. Myeloid cells activate iNKT cells to produce IL-4 in the thymic medulla.Proceedings of the National Academy of Sciences of the United States of America · 2019
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  12. Article
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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 3 institutions in 1 country.

Eleanor Clancy-ThompsonDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA 02215.
Gui Zhen ChenDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA 02215.ORCID 0000-0002-5483-7178
Paul M TylerDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA 02215.
Mariah M ServosDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA 02215.
Marta BarisaWhitehead Institute for Biomedical Research, Cambridge, MA 02242; and.ORCID 0000-0001-7846-6810
Patrick J BrennanDivision of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, MA 02215.
Hidde L PloeghWhitehead Institute for Biomedical Research, Cambridge, MA 02242; and.
Stephanie K DouganDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA 02215; Stephanie_dougan@dfci.harvard.edu.
Dana-Farber Cancer Institute · USWhitehead Institute for Biomedical Research · USBrigham and Women's Hospital · US

Funding

Cancer Immunology Training GrantT32CA207021 · NCI · DANA-FARBER CANCER INST · PI WUCHERPFENNIG, KAI W · 2016 to 2020
$2.4M
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
NCI NIH HHS T32 CA207021NIAID NIH HHS K08 AI102945
6 · The paper itself

Abstract

Invariant NKT (iNKT) cell functional subsets are defined by key transcription factors and output of cytokines, such as IL-4, IFN-γ, IL-17, and IL-10. To examine how TCR specificity determines iNKT function, we used somatic cell nuclear transfer to generate three lines of mice cloned from iNKT nuclei. Each line uses the invariant Vα14Jα18 TCRα paired with unique Vβ7 or Vβ8.2 subunits. We examined tissue homing, expression of PLZF, T-bet, and RORγt, and cytokine profiles and found that, although monoclonal iNKT cells differentiated into all functional subsets, the NKT17 lineage was reduced or expanded depending on the TCR expressed. We examined iNKT thymic development in limited-dilution bone marrow chimeras and show that higher TCR avidity correlates with higher PLZF and reduced T-bet expression. iNKT functional subsets showed distinct tissue distribution patterns. Although each individual monoclonal TCR showed an inherent subset distribution preference that was evident across all tissues examined, the iNKT cytokine profile differed more by tissue of origin than by TCR specificity.

Indexed as

Cell DifferentiationAnimalsB-LymphocytesCytokinesCytotoxicity, ImmunologicInterleukin-10Interleukin-17Kruppel-Like Transcription FactorsMiceMice, Inbred C57BLNatural Killer T-CellsNuclear Receptor Subfamily 1, Group F, Member 3Nuclear Transfer TechniquesOrgan SpecificityPromyelocytic Leukemia Zinc Finger ProteinReceptors, Antigen, T-Cell, alpha-betaCytokinesInterleukin-10Interleukin-17Kruppel-Like Transcription FactorsNuclear Receptor Subfamily 1, Group F, Member 3Promyelocytic Leukemia Zinc Finger ProteinReceptors, Antigen, T-Cell, alpha-betaT-bet Transcription FactorT-Box Domain ProteinsZbtb16 protein, mouse

Identifiers

PMID28576977
PMCPMC5518629
OpenAlexW2620884328

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.