Evidence map›Paper›PMID 21946866›Full record

ReviewThrombosis and haemostasis2011

Natural killer T cells in lipoprotein metabolism and atherosclerosis.

G S Getz, P A Vanderlaan, C A Reardon

Abstract readReview
In one paragraph

Review in Thrombosis and haemostasis, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. Apolipoprotein E in Cardiometabolic and Neurological Health and Diseases.International journal of molecular sciences · 2022
    Review
  2. Review
  3. Article
  4. Natural killer T cells in atherosclerosis.Nature reviews. Cardiology · 2017
    Review
  5. Animal models of atherosclerosis.Biomedical reports · 2017
    Article
  6. Review
  7. Article
  8. Engineering nanomaterials to address cell-mediated inflammation in atherosclerosis.Regenerative engineering and translational medicine · 2016
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Animal models of atherosclerosis.Arteriosclerosis, thrombosis, and vascular biology · 2012
    Review
  20. 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

3 authors at 1 institution in 1 country.

G S GetzUniversity of Chicago, Chicago, IL 60637, USA. g-getz@uchicago.edu
P A Vanderlaan
C A Reardon
University of Chicago · US

Funding

NKT cells in lipoprotein Metabolism and atherosclerosisR01HL088420 · NHLBI · UNIVERSITY OF CHICAGO · PI GETZ, GODFREY SHALOM · 2008 to 2011
$1.5M
NHLBI NIH HHS HL088420NHLBI NIH HHS R01 HL088420
6 · The paper itself

Abstract

Cells of both the innate and adaptive immune system participate in the development of atherosclerosis, a chronic inflammatory disorder of medium and large arteries. Natural killer T (NKT) cells express surface markers characteristic of natural killer cells and conventional T cells and bridge the innate and adaptive immune systems. The development and activation of NKT cells is dependent upon CD1d, a MHC-class I-type molecule that presents lipids, especially glycolipids to the T cell receptors on NKT cells. There are two classes of NKT cells; invariant NKT cells that express a semi-invariant T cell receptor and variant NKT cells. This review summarises studies in murine models in which the effect of the activation, overexpression or deletion of NKT cells or only invariant NKT cells on atherosclerosis has been examined.

Indexed as

Adaptive ImmunityAnimalsAntigens, CD1dArteriesAtherosclerosisHumansImmunity, InnateInflammationLipoproteinsNatural Killer T-CellsPhenotypeAntigens, CD1dLipoproteins

Identifiers

PMID21946866
PMCPMC3696188
OpenAlexW2146087639

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.