Evidence map›Paper›PMID 22628430›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2012

Marked acceleration of atherosclerosis after Lactobacillus casei-induced coronary arteritis in a mouse model of Kawasaki disease.

Shuang Chen, Youngho Lee, Timothy R Crother, Michael Fishbein, Wenxuan Zhang, Atilla Yilmaz, Kenichi Shimada, Danica J Schulte, Thomas J A Lehman, Prediman K Shah and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  11. Characterization of the T Cell Response toFrontiers in pediatrics · 2021
    Article
  12. Review
  13. Antibodies and Immunity During Kawasaki Disease.Frontiers in cardiovascular medicine · 2020
    Review
  14. Article
  15. Article
  16. Review
  17. Kawasaki disease: a matter of innate immunity.Clinical and experimental immunology · 2016
    Review
  18. Article
  19. Article
  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

11 authors at 4 institutions in 2 countries.

Shuang ChenDavid Geffen School of Medicine at the University of California, Division of Pediatric Infectious Diseases and Immunology, Burns and Allen Research Institute, Cedars-Sinai Medical Center, 8700 Beverly Blvd, Los Angeles, CA 90048, USA.
Youngho Lee
Timothy R Crother
Michael Fishbein
Wenxuan Zhang
Atilla Yilmaz
Kenichi Shimada
Danica J Schulte
Thomas J A Lehman
Prediman K Shah
Moshe Arditi
Cornell University · USUniversity of California, Los Angeles · USHospital for Special Surgery · USJena University Hospital · DE

Funding

Role of IL-1 in Bacterial ligand-induced vasculitis and myocarditisR01AI072726 · NIAID · CEDARS-SINAI MEDICAL CENTER · PI ARDITI, MOSHE · 2008 to 2020
$4.5M
MOLECULAR PATHOGENESIS OF CHLAMYDIA-INDUCED ATHEROGENESIR01HL066436 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI ARDITI, MOSHE · 2001 to 2013
$3.6M
Innate Immunity and Mouse Model of Kawasaki DiseaseK08AI070162 · NIAID · CEDARS-SINAI MEDICAL CENTER · PI SCHULTE, DANICA JENINE · 2007 to 2010
$508k
NHLBI NIH HHS HL66436NHLBI NIH HHS R01 HL066436NIAID NIH HHS AI070162NIAID NIH HHS AI1072726NIAID NIH HHS K08 AI070162NIAID NIH HHS R01 AI072726
6 · The paper itself

Abstract

objectiveThe purpose of this study was to investigate whether Lactobacillus casei cell wall extract-induced Kawasaki disease (KD) accelerates atherosclerosis in hypercholesterolemic mice. Method and Results- Apolipoprotein E knockout or low-density lipoprotein receptor knockout mice were injected with Lactobacillus casei cell wall extract (KD mice) or PBS, fed high-fat diet for 8 weeks, and atherosclerotic lesions in aortic sinuses, arch (AC), and whole aorta were assessed. KD mice had larger, more complex aortic lesions with abundant collagen, and both extracellular and intracellular lipid and foam cells, compared with lesions in control mice despite similar cholesterol levels. Both apolipoprotein E knockout KD and low-density lipoprotein receptor knockout KD mice showed dramatic acceleration in atherosclerosis versus controls, with increases in en face aortic atherosclerosis and plaque size in both the aortic sinuses and AC plaques. Accelerated atherosclerosis was associated with increased circulating interleukin-12p40, interferon-γ, tumor necrosis factor-α, and increased macrophage, dendritic cell, and T-cell recruitment in lesions. Furthermore, daily injections of the interleukin-1Ra, which inhibits Lactobacillus casei cell wall extract-induced KD vasculitis, prevented the acceleration of atherosclerosis.

conclusionsOur results suggest an important pathophysiologic link between coronary arteritis/vasculitis in the KD mouse model and subsequent atherosclerotic acceleration, supporting the concept that a similar relation may also be present in KD patients. These results also suggest that KD in childhood may predispose to accelerated and early atherosclerosis as adults.

Indexed as

AnimalsApolipoproteins EArteritisAtherosclerosisCoronary Artery DiseaseDendritic CellsDisease Models, AnimalInterleukin 1 Receptor Antagonist ProteinLacticaseibacillus caseiMiceMice, Inbred C57BLMucocutaneous Lymph Node SyndromePlaque, AtheroscleroticReceptors, LDLApolipoproteins EInterleukin 1 Receptor Antagonist ProteinReceptors, LDL

Identifiers

PMID22628430
PMCPMC3480341
OpenAlexW2152760400

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.