Evidence map›Paper›PMID 30502719›Full record

ReviewMolecular immunology2019

The ins and outs of type I iNKT cell development.

Susannah C Shissler, Tonya J Webb

Abstract readReview
In one paragraph

Review in Molecular immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Novel lipid antigens for NKT cells in cancer.Frontiers in immunology · 2023
    Review
  13. Review
  14. Metabolic regulation of T cell development.Frontiers in immunology · 2022
    Review
  15. Article
  16. Genetic Analysis of iNKT Cell Development and Function.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  17. Article
  18. A DesignedAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
  19. Review
  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

2 authors at 1 institution in 1 country.

Susannah C ShisslerDepartment of Microbiology and Immunology, University of Maryland School of Medicine, 685 W. Baltimore St. HSF-1 Room 380, Baltimore, MD 21201, USA. Electronic address: susannah.shissler@umaryland.edu.
Tonya J WebbDepartment of Microbiology and Immunology, University of Maryland School of Medicine, 685 W. Baltimore St. HSF-1 Room 380, Baltimore, MD 21201, USA.
University of Maryland, Baltimore · US

Funding

IMMUNITY AND INFECTIONT32AI007540 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KAPER, JAMES B · 1998 to 2018
$2.2M
Generation of NKT cells from adult stem cells for adoptive immunotherapyR21CA184469 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI WEBB, TONYA J. · 2015 to 2016
$367k
NKT cells with chimeric antigen receptorsR21CA199544 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI WEBB, TONYA J. · 2015 to 2016
$367k
NCI NIH HHS R21 CA184469NCI NIH HHS R21 CA199544NIAID NIH HHS T32 AI007540
6 · The paper itself

Abstract

Natural killer T (NKT) cells are innate-like lymphocytes that bridge the gap between the innate and adaptive immune responses. Like innate immune cells, they have a mature, effector phenotype that allows them to rapidly respond to threats, compared to adaptive cells. NKT cells express T cell receptors (TCRs) like conventional T cells, but instead of responding to peptide antigen presented by MHC class I or II, NKT cell TCRs recognize glycolipid antigen in the context of CD1d. NKT cells are subdivided into classes based on their TCR and antigen reactivity. This review will focus on type I iNKT cells that express a semi invariant Vα14Jα18 TCR and respond to the canonical glycolipid antigen, α-galactosylceramide. The innate-like effector functions of these cells combined with their T cell identity make their developmental path quite unique. In addition to the extrinsic factors that affect iNKT cell development such as lipid:CD1d complexes, co-stimulation, and cytokines, this review will provide a comprehensive delineation of the cell intrinsic factors that impact iNKT cell development, differentiation, and effector functions - including TCR rearrangement, survival and metabolism signaling, transcription factor expression, and gene regulation.

Indexed as

Antigen PresentationAnimalsAntigens, CD1dCytokinesGene Expression RegulationGene Rearrangement, alpha-Chain T-Cell Antigen ReceptorGlycolipidsHistocompatibility Antigens Class IHumansNatural Killer T-CellsReceptors, Antigen, T-Cell, alpha-betaTranscription, GeneticAntigens, CD1dCD1D protein, humanCytokinesGlycolipidsHistocompatibility Antigens Class IReceptors, Antigen, T-Cell, alpha-betaCD1diNKTInnate lymphocytesNatural killer TNKT cellsT cell development

Identifiers

PMID30502719
PMCPMC6331266
OpenAlexW2902597412

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.