Evidence map›Paper›PMID 18445005›Full record

ArticleImmunology2008

Widespread natural variation in murine natural killer T-cell number and function.

Stacia L Rymarchyk, Hayden Lowenstein, Jana Mayette, Samantha R Foster, David E Damby, Isaac W Howe, Idil Aktan, Russell E Meyer, Matthew E Poynter, Jonathan E Boyson

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

26 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Glycolipid-peptide conjugate vaccines elicit CD8Clinical & translational immunology · 2022
    Article
  4. Development of αβ T Cells with Innate Functions.Advances in experimental medicine and biology · 2022
    Article
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  6. Review
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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

10 authors at 1 institution in 1 country.

Stacia L RymarchykDepartment of Surgery, Univeristy of Vermont College of Medicine, Burlington, VT 05405, USA.
Hayden Lowenstein
Jana Mayette
Samantha R Foster
David E Damby
Isaac W Howe
Idil Aktan
Russell E Meyer
Matthew E Poynter
Jonathan E Boyson
University of Vermont · US

Funding

WEIGHT LOSS & ASTHMAP20RR015557 · NCRR · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI RINCON, MERCEDES · 2000 to 2009
$21.4M
VERMONT IMMUNOBIOLOIGY/ INFECTIOUS DISEASES CENTERP20RR021905 · NCRR · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI HILL, JACK · 2006 to 2011
$14.5M
CD1D-Restricted T cells and Pregnancy LossR01AI067897 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI BOYSON, JONATHAN E · 2007 to 2010
$1.5M
NCRR NIH HHS P20 RR015557NCRR NIH HHS P20 RR021905NCRR NIH HHS P20RR021905NCRR NIH HHS P20RR15557NIAID NIH HHS R01 AI067897NIAID NIH HHS R01AI067897
6 · The paper itself

Abstract

Natural killer T (NKT) cells comprise a novel T-lymphocyte subset that can influence a wide variety of immune responses through their ability to secrete large amounts of a variety of cytokines. Although variation in NKT-cell number and function has been extensively studied in autoimmune disease-prone mice, in which it has been linked to disease susceptibility, relatively little is known of the natural variation of NKT-cell number and function among normal inbred mouse strains. Here, we demonstrate strain-dependent variation in the susceptibility of C57BL/6J and BALB/cJ mice to NKT-mediated airway hyperreactivity, which correlated with significant increases in serum interleukin-4 (IL-4) and IL-13 elicited by the synthetic glycosphingolipid alpha-galactosylceramide. Examination of NKT-cell function revealed a significantly greater frequency of cytokine-producing NKT cells in C57BL/6J versus BALB/cJ mice as well as significant differences in the kinetics of NKT-cell cytokine production. Extension of this analysis to a panel of inbred mouse strains indicated that variability in NKT-cell cytokine production was widespread. Similarly, an examination of NKT-cell frequency revealed a significantly greater number of liver NKT cells in the C57BL/6J mice versus BALB/cJ mouse livers. Again, examination of a panel of inbred mouse strains revealed that liver NKT-cell numbers were quite variable, spanning over a 100-fold range. Taken together, these results demonstrate the presence of widespread natural variation in NKT-cell number and function among common inbred mouse strains, which may have implications for the examination of the influence of NKT cells in immune responses and disease pathogenesis among different genetic backgrounds.

Indexed as

AnimalsCells, CulturedCytokinesGalactosylceramidesGenetic Predisposition to DiseaseInterleukin-13Interleukin-4LiverLymphocyte CountMiceMice, Inbred StrainsNatural Killer T-CellsRespiratory HypersensitivitySpecies Specificityalpha-galactosylceramideCytokinesGalactosylceramidesInterleukin-13Interleukin-4

Identifiers

PMID18445005
PMCPMC2669137
OpenAlexW2011955726

What OpenQuestion holds

Textmetadata
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.