Evidence map›Paper›PMID 31320700›Full record

ArticleScientific reports2019

Interleukin-12 and -23 blockade mitigates elastase-induced abdominal aortic aneurysm.

Huimin Yan, Ying Hu, Antonina Akk, Karen Ye, John Bacon, Christine T N Pham

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  9. The mechanism and therapy of aortic aneurysms.Signal transduction and targeted therapy · 2023
    Review
  10. Review
  11. Role of Extracellular Matrix and Inflammation in Abdominal Aortic Aneurysm.International journal of molecular sciences · 2022
    Review
  12. Review
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  14. Article
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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

6 authors at 1 institution in 1 country.

Huimin YanJohn Cochran VA Medical Center, Saint Louis, Missouri, USA.
Ying HuJohn Cochran VA Medical Center, Saint Louis, Missouri, USA.
Antonina AkkJohn Cochran VA Medical Center, Saint Louis, Missouri, USA.
Karen YeJohn Cochran VA Medical Center, Saint Louis, Missouri, USA.
John BaconJohn Cochran VA Medical Center, Saint Louis, Missouri, USA.
Christine T N PhamJohn Cochran VA Medical Center, Saint Louis, Missouri, USA. cpham@wustl.edu.ORCID http://orcid.org/0000-0003-1127-3699
Washington University in St. Louis · US

Funding

Washington University Rheumatic DiseasesResearch Resource-based CenterP30AR073752 · NIAMS · WASHINGTON UNIVERSITY · PI Alfred Hyoungju Kim · 2018 to 2026
$7.6M
Inhibition of NF-kB with siRNA/Peptide Nanoparticles for Arthritis TreatmentR01AR067491 · NIAMS · WASHINGTON UNIVERSITY · PI PHAM, CHRISTINE T., WICKLINE, SAMUEL A · 2015 to 2019
$1.8M
Immune-mediated pathways in pathogenesis of abdominal aortic aneurysmI01BX002714 · VA · ST. LOUIS VA MEDICAL CENTER · PI PHAM, CHRISTINE T. · 2015 to 2020
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BLRD VA I01 BX002714NIAMS NIH HHS P30 AR073752NIAMS NIH HHS R01 AR067491
6 · The paper itself

Abstract

Macrophages play an important role in the inflammatory process that contributes to the development of abdominal aortic aneurysm (AAA). Studies of human and mouse AAA tissue reveal expanded populations of macrophages producing an abundance of pro-inflammatory cytokines, including TNF-α, IL-12p40 and high level of metalloprotease 9 (MMP-9) at the late stages of disease. Herein, we show that blockade of IL-12p40 in the early phase of aneurysm development suppresses macrophage expansion, inflammatory cytokine and MMP-9 production and mitigates AAA development. Since IL-12 and IL-23 are related cytokines that share the common p40 subunit, we also evaluate the effect of direct IL-23 blockade on the development of AAA. Specific IL-23p19 blockade prevents AAA progression with the same efficiency as IL-12p40 antagonism, suggesting that the efficacy of anti-IL-12p40 treatment may reflect IL-23 blockade. IL-12p40 and IL-23p19 are also abundantly expressed in human AAA tissue. Our findings have potential translational value since IL-12p40 and IL-23p19 antagonists already exist as FDA-approved therapeutics for various chronic inflammatory conditions.

Indexed as

AnimalsAortic Aneurysm, AbdominalCytokinesDisease Models, AnimalHumansInflammation MediatorsInterleukin-12Interleukin-23MacrophagesMaleMiceMice, Inbred C57BLPancreatic ElastaseSignal TransductionCytokinesInflammation MediatorsInterleukin-12Interleukin-23Pancreatic Elastase

Identifiers

PMID31320700
PMCPMC6639297
OpenAlexW2958054972

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.