Evidence map›Paper›PMID 19290924›Full record

ReviewImmunological reviews2009

The Tec kinases Itk and Rlk regulate conventional versus innate T-cell development.

Amanda L Prince, Catherine C Yin, Megan E Enos, Martin Felices, Leslie J Berg

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
  2. Review
  3. Development of αβ T Cells with Innate Functions.Advances in experimental medicine and biology · 2022
    Article
  4. Review
  5. Article
  6. Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
    Article
  7. Article
  8. Review
  9. ERK Signaling Controls Innate-like CD8Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  10. Article
  11. Review
  12. NFAT2 Regulates Generation of Innate-Like CD8Frontiers in immunology · 2016
    Article
  13. Article
  14. Targets for Ibrutinib Beyond B Cell Malignancies.Scandinavian journal of immunology · 2015
    Review
  15. Review
  16. Review
  17. Targeting Interleukin-2-Inducible T-cell Kinase (ITK) in T-Cell Related Diseases.Postdoc journal : a journal of postdoctoral research and postdoctoral affairs · 2014
    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

5 authors at 1 institution in 1 country.

Amanda L PrinceDepartment of Pathology, University of Massachussets Medical School, Worcester, MA 01655, USA.
Catherine C Yin
Megan E Enos
Martin Felices
Leslie J Berg
University of Massachusetts Chan Medical School · US

Funding

IMMUNOBIOLOGY OF JAK3-DEFICIENT MICER01AI046564 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BERG, LESLIE JOAN · 2000 to 2010
$3.1M
Tec family tyrosine kinases in T cell signalingR01AI037584 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BERG, LESLIE JOAN · 1995 to 2009
$2.8M
Tec Kinases ltk and RlK in Mast Cell SignalingR01AI066118 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BERG, LESLIE JOAN · 2006 to 2009
$1.6M
NIAID NIH HHS AI37584NIAID NIH HHS AI46564NIAID NIH HHS AI66118NIAID NIH HHS R01 AI037584NIAID NIH HHS R01 AI046564NIAID NIH HHS R01 AI066118
6 · The paper itself

Abstract

Tec family kinases are important components of antigen receptor signaling pathways in B cells, T cells, and mast cells. In T cells, three members of this family, inducible T-cell kinase (Itk), resting lymphocyte kinase (Rlk), and Tec, are expressed. In the absence of Itk and Rlk, T-cell receptor signaling is impaired, with defects in mitogen-activated protein kinase activation, Ca(2+) mobilization, and actin polymerization. During T-cell development in the thymus, no role has been found for these kinases in the CD4(+) versus CD8(+) T-cell lineage decision; however, several studies indicate that Itk and Rlk contribute to the signaling leading to positive and negative selection. In addition, we and others have recently described an important role for Itk and Rlk in the development of conventional as opposed to innate CD4(+) and CD8(+) T cells. Natural killer T and gammadelta T-cell populations are also altered in Itk- and Rlk/Itk-deficient mice. These findings strongly suggest that the strength of T-cell receptor signaling during development determines whether T cells mature into conventional versus innate lymphocyte lineages. This lineage decision is also influenced by signaling via signaling lymphocytic activation molecule (SLAM) family receptors. Here we discuss these two signaling pathways that each contribute to conventional versus innate T-cell lineage commitment.

Indexed as

AnimalsCell DifferentiationHumansProtein-Tyrosine KinasesSignal TransductionThymus GlandT-Lymphocytesemt protein-tyrosine kinaseProtein-Tyrosine KinasesTec protein-tyrosine kinase

Identifiers

PMID19290924
PMCPMC2669323
OpenAlexW1998096690

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.