Evidence map›Paper›PMID 25313857›Full record

ArticlePloS one2014

γδT cells are prevalent in the proximal aorta and drive nascent atherosclerotic lesion progression and neutrophilia in hypercholesterolemic mice.

Duc M Vu, Albert Tai, Jeffrey B Tatro, Richard H Karas, Brigitte T Huber, Debbie Beasley

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. 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
1.5field-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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
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  7. Review
  8. Clonally expanded memory CD8Nature aging · 2023
    Article
  9. Review
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  11. Review
  12. Increase of Vδ2Immune network · 2021
    Article
  13. Adaptive Immune Responses in Human Atherosclerosis.International journal of molecular sciences · 2020
    Review
  14. T cell subsets and functions in atherosclerosis.Nature reviews. Cardiology · 2020
    Review
  15. Article
  16. Atherosclerosis in the single-cell era.Current opinion in lipidology · 2018
    Review
  17. T Cells in Atherosclerosis in Ldlr-/- and Apoe-/- Mice.Journal of immunological sciences · 2018
    Article
  18. Review
  19. Article
  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

6 authors at 2 institutions in 1 country.

Duc M VuMolecular Cardiology Research Institute, Tufts Medical Center, Boston, Massachusetts, United States of America.
Albert TaiDepartment of Integrative Physiology and Pathobiology, Tufts University School of Medicine, Boston, Massachusetts, United States of America.
Jeffrey B TatroDivision of Endocrinology, Diabetes and Metabolism, Tufts Medical Center, Boston, Massachusetts, United States of America.
Richard H KarasMolecular Cardiology Research Institute, Tufts Medical Center, Boston, Massachusetts, United States of America.
Brigitte T HuberDepartment of Integrative Physiology and Pathobiology, Tufts University School of Medicine, Boston, Massachusetts, United States of America.
Debbie BeasleyMolecular Cardiology Research Institute, Tufts Medical Center, Boston, Massachusetts, United States of America.
Tufts Medical Center · USTufts University · US

Funding

Tufts Clinical and Translational Research InstituteUL1TR001064 · NCATS · TUFTS UNIVERSITY BOSTON · PI SELKER, HARRY P. · 2013 to 2017
$26.4M
AUTOCRINE ROLE OF CYTOKINES IN VASCULAR SMOOTH MUSCLER01HL047569 · NHLBI · TUFTS MEDICAL CENTER · PI BEASLEY, DEBBIE · 1992 to 2010
$3.1M
Atherogenic role of T cell modulation by intestinal bacteriaR21HL113732 · NHLBI · TUFTS MEDICAL CENTER · PI BEASLEY, DEBBIE · 2012 to 2013
$428k
NCATS NIH HHS UL1 TR001064NCATS NIH HHS UL1TR001064NHLBI NIH HHS R01 HL047569NHLBI NIH HHS R01 HL113732NHLBI NIH HHS R01 HL47569NHLBI NIH HHS R21 HL113732
6 · The paper itself

Abstract

Unique innate immunity-linked γδT cells have been seen in early human artery lesions, but their role in lesion development has received little attention. Here we investigated whether γδT cells modulate atherogenesis in apolipoprotein E-deficient (ApoE KO) mice. We found that γδT cell numbers were markedly increased in the proximal aorta of ApoE-deficient vs. wild-type mice during early atherogenesis, particularly in the aortic root and arch, where they comprised most of the T cells and lesion progression is most rapid. γδT cells infiltrated intimal lesions in ApoE KO mice, but only the adventitia in wild-type mice, and were more prevalent than CD4+ T cells in early nascent lesions, as evaluated by en face confocal microscopy. These aortic γδT cells produced IL-17, but not IFN-γ, analyzed by ex vivo FACS. Furthermore, aortic arch lipid accumulation correlated strongly with abundance of IL-17-expressing splenic γδT cells in individual ApoE KO mice. To investigate the role of these γδT cells in early atherogenesis, we analyzed ApoE/γδT double knockout (DKO) compared to ApoE KO mice. We observed reduced early intimal lipid accumulation at sites of nascent lesion formation, both in chow-fed (by 40%) and Western diet-fed (by 44%) ApoE/γδT DKO mice. In addition, circulating neutrophils were drastically reduced in these DKO mice on Western diet, while expansion of inflammatory monocytes and splenic Th1 or Th17 lymphocytes was not affected. These data reveal, for the first time, a pathogenic role of γδT cells in early atherogenesis in ApoE KO mice, by mechanisms likely to involve their IL-17 production and induction of neutrophilia. Targeting γδT cells thus might offer therapeutic benefit in atherosclerosis or other inflammatory vascular diseases.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticAortaAorta, ThoracicApolipoproteins EAtherosclerosisCD68 MoleculeDiet, High-FatDisease Models, AnimalDisease ProgressionElastinHypercholesterolemiaInterleukin-17Leukocyte DisordersLipidsAntigens, CDAntigens, Differentiation, MyelomonocyticApolipoproteins ECD68 antigen, humanCD68 MoleculeElastinInterleukin-17LipidsReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID25313857
PMCPMC4196850
OpenAlexW2010218102

What OpenQuestion holds

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Registered trials

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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.