Evidence map›Paper›PMID 23800654›Full record

ReviewInternational immunopharmacology2013

Fine tuning a well-oiled machine: Influence of NK1.1 and NKG2D on NKT cell development and function.

Sunil K Joshi, Mark L Lang

Abstract readReview
In one paragraph

Review in International immunopharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. License to Kill: When iNKT Cells Are Granted the Use of Lethal Cytotoxicity.International journal of molecular sciences · 2020
    Review
  3. [Expression of regulatory T cells and natural killer T cells in peripheral blood of children with Wilms tumor].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2016
    Article
  4. Article
  5. Review
  6. Article
  7. Natural killer T (NKT) cells in autoimmune hepatitis.Current opinion in immunology · 2013
    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

2 authors at 2 institutions in 1 country.

Sunil K JoshiDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA. skjoshi@odu.edu
Mark L Lang
Old Dominion University · USUniversity of Oklahoma Health Sciences Center · US

Funding

Translation of immunologic technologies from basic research into pre-clinical nonU19AI062629 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI COGGESHALL, KENNETH MARK · 2004 to 2023
$56.2M
Regulation of humoral immunity by NKT cellsR01AI078993 · NIAID · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LANG, MARK L · 2009 to 2013
$1.6M
Regulation of humoral immunity by NKT cellsR56AI078993 · NIAID · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LANG, MARK L · 2014 to 2014
$404k
NIAID NIH HHS AI062629NIAID NIH HHS AI078993NIAID NIH HHS R01 AI078993NIAID NIH HHS R56 AI078993NIAID NIH HHS U19 AI062629
6 · The paper itself

Abstract

Natural killer T cells (NKT) represent a group of CD1d-restricted T-lineage cells that provide a functional interface between innate and adaptive immune responses in infectious disease, cancer, allergy and autoimmunity. There have been remarkable advances in understanding the molecular events that underpin NKT development in the thymus and in the complex array of functions in the periphery. Most functional studies have focused on activation of T cell antigen receptors expressed by NKT cells and their responses to CD1d presentation of glycolipid and related antigens. Receiving less attention has been several molecules that are hallmarks of Natural Killer (NK) cells, but nonetheless expressed by NKT cells. These include several activating and inhibitory receptors that may fine-tune NKT development and survival, as well as activation via antigen receptors. Herein, we review the possible roles of the NK1.1 and NKG2D receptors in regulating development and function of NKT cells in health and disease. We suggest that pharmacological alteration of NKT activity should consider the potential complexities commensurate with NK1.1 and NKG2D expression.

Indexed as

Adaptive ImmunityAnimalsAntigens, LyAutoimmune DiseasesCytotoxicity, ImmunologicHumansImmunity, InnateInfectionsLymphocyte ActivationLymphocyte SubsetsMiceNatural Killer T-CellsNeoplasmsNK Cell Lectin-Like Receptor Subfamily BNK Cell Lectin-Like Receptor Subfamily KReceptor Cross-TalkAntigens, LyKlrb1c protein, mouseKlrk1 protein, mouseNK Cell Lectin-Like Receptor Subfamily BNK Cell Lectin-Like Receptor Subfamily KAdaptive immunityNK1.1NKG2DNKT cellsPathogenesis

Identifiers

PMID23800654
PMCPMC3759579
OpenAlexW2053618310

What OpenQuestion holds

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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.