Evidence map›Paper›PMID 24928994›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Innate PLZF+CD4+ αβ T cells develop and expand in the absence of Itk.

Amanda L Prince, Levi B Watkin, Catherine C Yin, Liisa K Selin, Joonsoo Kang, Pamela L Schwartzberg, Leslie J Berg

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The impact of the gut microbiota on T cell ontogeny in the thymus.Cellular and molecular life sciences : CMLS · 2022
    Review
  5. Intestinal microbes influence development of thymic lymphocytes in early life.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  6. Review
  7. Article
  8. Article
  9. Id2 Collaborates with Id3 To Suppress Invariant NKT and Innate-like Tumors.Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Itk signals promote neuroinflammation by regulating CD4+ T-cell activation and trafficking.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  15. 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

7 authors at 2 institutions in 1 country.

Amanda L PrinceDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01655; and.
Levi B WatkinDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01655; and.
Catherine C YinDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01655; and.
Liisa K SelinDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01655; and.
Joonsoo KangDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01655; and.
Pamela L SchwartzbergNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20814.
Leslie J BergDepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01655; and Leslie.Berg@umassmed.edu.
University of Massachusetts Chan Medical School · USNational Human Genome Research Institute · US

Funding

Genetic and Biochemical Approaches to Tyrosine Kinase FunctionZIAHG000123 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI SCHWARTZBERG, PAMELA · 2009 to 2018
$20.8M
T cell and transgenic core U19AI109858 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HUSEBY, ERIC S · 2014 to 2018
$11.9M
TRAINING IN IMMUNOLOGY (COMPETITIVE RENEWAL OF AI07439)T32AI007349 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STERN, LAWRENCE J. · 1989 to 2024
$4.5M
Gene circuits programming IL-17 production in innate lymphocytesR01AI101301 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KANG, JOONSOO · 2013 to 2017
$2.1M
Plasticity of T helper cell differentiationR01AI101048 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BERG, LESLIE JOAN · 2013 to 2016
$1.6M
Regulation of conventional versus innate CD8+ T cell developmentR01AI084987 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BERG, LESLIE JOAN · 2010 to 2013
$1.6M
NIAID NIH HHS AI084987NIAID NIH HHS R01 AI084987NIAID NIH HHS R01 AI101048NIAID NIH HHS R01 AI101301NIAID NIH HHS T32 AI007349NIAID NIH HHS U19 AI109858
6 · The paper itself

Abstract

T cell development in the thymus produces multiple lineages of cells, including innate T cells. Studies in mice harboring alterations in TCR signaling proteins or transcriptional regulators have revealed an expanded population of CD4(+) innate T cells in the thymus that produce IL-4 and express the transcription factor promyelocytic leukemia zinc finger (PLZF). In these mice, IL-4 produced by the CD4(+)PLZF(+) T cell population leads to the conversion of conventional CD8(+) thymocytes into innate CD8(+) T cells resembling memory T cells expressing eomesodermin. The expression of PLZF, the signature invariant NKT cell transcription factor, in these innate CD4(+) T cells suggests that they might be a subset of αβ or γδ TCR(+) NKT cells or mucosal-associated invariant T (MAIT) cells. To address these possibilities, we characterized the CD4(+)PLZF(+) innate T cells in itk(-/-) mice. We show that itk(-/-) innate PLZF(+)CD4(+) T cells are not CD1d-dependent NKT cells, MR1-dependent MAIT cells, or γδ T cells. Furthermore, although the itk(-/-) innate PLZF(+)CD4(+) T cells express αβ TCRs, neither β2-microglobulin-dependent MHC class I nor any MHC class II molecules are required for their development. In contrast to invariant NKT cells and MAIT cells, this population has a highly diverse TCRα-chain repertoire. Analysis of peripheral tissues indicates that itk(-/-) innate PLZF(+)CD4(+) T cells preferentially home to spleen and mesenteric lymph nodes owing to increased expression of gut-homing receptors, and that their expansion is regulated by commensal gut flora. These data support the conclusion that itk(-/-) innate PLZF(+)CD4(+) T cells are a novel subset of innate T cells.

Indexed as

Cell ProliferationAnimalsAntigens, CD1dbeta 2-MicroglobulinCD4-Positive T-LymphocytesCell DifferentiationCells, CulturedFlow CytometryGene ExpressionH-2 AntigensInterleukin-4Kruppel-Like Transcription FactorsLymph NodesMiceMice, Inbred C57BLMice, KnockoutAntigens, CD1dbeta 2-Microglobulinemt protein-tyrosine kinaseH-2 AntigensInterleukin-4Kruppel-Like Transcription FactorsPromyelocytic Leukemia Zinc Finger ProteinProtein-Tyrosine KinasesReceptors, Antigen, T-Cell, alpha-betaZbtb16 protein, mouse

Identifiers

PMID24928994
PMCPMC4083617
OpenAlexW1913194466

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.