Evidence map›Paper›PMID 29754419›Full record

ArticleImmunology and cell biology2018

Integration of T-cell receptor, Notch and cytokine signals programs mouse γδ T-cell effector differentiation.

Payam Zarin, Tracy Sh In, Edward Ly Chen, Jastaranpreet Singh, Gladys W Wong, Mahmood Mohtashami, David L Wiest, Michele K Anderson, Juan Carlos Zúñiga-Pflücker

Open access · hybridAbstract read
In one paragraph

Article in Immunology and cell biology, 2018. 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
1.5field-weighted citation impact, top 19% 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, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. HEB collaborates with TCR signaling to upregulatebioRxiv : the preprint server for biology · 2025
    Article
  5. T Cell Development: From T-Lineage Specification to Intrathymic Maturation.Advances in experimental medicine and biology · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Fetal Thymic Organ Culture (FTOC) Optimized for Gamma-Delta T Cell Studies.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Payam ZarinDepartment of Immunology, University of Toronto, and Sunnybrook Research Institute, 2075 Bayview Ave., Toronto, ON, M4N 3M5, Canada.
Tracy Sh InDepartment of Immunology, University of Toronto, and Sunnybrook Research Institute, 2075 Bayview Ave., Toronto, ON, M4N 3M5, Canada.
Edward Ly ChenDepartment of Immunology, University of Toronto, and Sunnybrook Research Institute, 2075 Bayview Ave., Toronto, ON, M4N 3M5, Canada.
Jastaranpreet SinghDepartment of Immunology, University of Toronto, and Sunnybrook Research Institute, 2075 Bayview Ave., Toronto, ON, M4N 3M5, Canada.
Gladys W WongDepartment of Immunology, University of Toronto, and Sunnybrook Research Institute, 2075 Bayview Ave., Toronto, ON, M4N 3M5, Canada.
Mahmood MohtashamiDepartment of Immunology, University of Toronto, and Sunnybrook Research Institute, 2075 Bayview Ave., Toronto, ON, M4N 3M5, Canada.
David L WiestBlood Cell Development and Cancer Keystone, Immune Cell Development and Host Defense Program, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA, 19111-2497, USA.
Michele K AndersonDepartment of Immunology, University of Toronto, and Sunnybrook Research Institute, 2075 Bayview Ave., Toronto, ON, M4N 3M5, Canada.
Juan Carlos Zúñiga-PflückerDepartment of Immunology, University of Toronto, and Sunnybrook Research Institute, 2075 Bayview Ave., Toronto, ON, M4N 3M5, Canada.ORCID 0000-0003-2538-3178
Sunnybrook Health Science Centre · CAFox Chase Cancer Center · US

Funding

The role of TCR, ligand, and signal strength in human γδ T cell developmentP01AI102853 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI CORNELIS MURRE · 2014 to 2026
$26.3M
CIHR FND-154332CIHR MOP-119538CIHR MOP-42387NIAID NIH HHS P01 AI102853
6 · The paper itself

Abstract

γδ T-cells perform a wide range of tissue- and disease-specific functions that are dependent on the effector cytokines produced by these cells. However, the aggregate signals required for the development of interferon-γ (IFNγ) and interleukin-17 (IL-17) producing γδ T-cells remain unknown. Here, we define the cues involved in the functional programming of γδ T-cells, by examining the roles of T-cell receptor (TCR), Notch, and cytokine-receptor signaling. KN6 γδTCR-transduced Rag2

Indexed as

Cell DifferentiationAnimalsInterferon-gammaInterleukin-17Lymphocyte ActivationMiceMice, Inbred BALB CMice, Inbred C57BLReceptors, Antigen, T-Cell, gamma-deltaReceptors, NotchSignal TransductionT-LymphocytesInterferon-gammaInterleukin-17Receptors, Antigen, T-Cell, gamma-deltaReceptors, NotchCytokinesNotchT-cell receptor

Identifiers

PMID29754419
PMCPMC6197911
OpenAlexW2802339654

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.