Evidence map›Paper›PMID 22965992›Full record

ArticleCirculation2012

Experimental abdominal aortic aneurysm formation is mediated by IL-17 and attenuated by mesenchymal stem cell treatment.

Ashish K Sharma, Guanyi Lu, Andrea Jester, William F Johnston, Yunge Zhao, Vanessa A Hajzus, M Reza Saadatzadeh, Gang Su, Castigliano M Bhamidipati, Gaurav S Mehta and 5 more

Erratum issuedAbstract read
In one paragraph

Article in Circulation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 93 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

93 citing papers in PubMed, 1 synthesis or guideline pooled it, 152 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Review
  7. Spatial Transcriptomics RevealsbioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Innovation in pathogenesis and management of aortic aneurysm.World journal of experimental medicine · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. The IL-17 family in diseases: from bench to bedside.Signal transduction and targeted therapy · 2023
    Review
  19. Article
  20. Article

33 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

15 authors at 1 institution in 1 country.

Ashish K SharmaDepartment of Surgery, University of Virginia Health System, Charlottesville, VA 22908, USA.
Guanyi Lu
Andrea Jester
William F Johnston
Yunge Zhao
Vanessa A Hajzus
M Reza Saadatzadeh
Gang Su
Castigliano M Bhamidipati
Gaurav S Mehta
Irving L Kron
Victor E Laubach
Michael P Murphy
Gorav Ailawadi
Gilbert R Upchurch
Indiana University – Purdue University Indianapolis · US

Funding

Cardiovascular Surgery Training ProgramT32HL007849 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI KRON, IRVING L., LAUBACH, VICTOR E · 1998 to 2025
$7.0M
Gender Differences in Experimental Aortic AneurysmsR01HL081629 · NHLBI · UNIVERSITY OF VIRGINIA · PI UPCHURCH, GILBERT RIVERS · 2007 to 2017
$4.1M
The Effects of KLF4 in experimental aortic aneurysm formationK08HL098560 · NHLBI · UNIVERSITY OF VIRGINIA · PI AILAWADI, GORAV · 2010 to 2014
$656k
NHLBI NIH HHS K08 HL098560NHLBI NIH HHS R01 HL081629NHLBI NIH HHS T32 HL007849
6 · The paper itself

Abstract

backgroundAbdominal aortic aneurysm (AAA) formation is characterized by inflammation, smooth muscle activation and matrix degradation. This study tests the hypothesis that CD4+ T-cell-produced IL-17 modulates inflammation and smooth muscle cell activation, leading to the pathogenesis of AAA and that human mesenchymal stem cell (MSC) treatment can attenuate IL-17 production and AAA formation. METHODS AND

resultsHuman aortic tissue demonstrated a significant increase in IL-17 and IL-23 expression in AAA patients compared with control subjects as analyzed by RT-PCR and ELISA. AAA formation was assessed in C57BL/6 (wild-type; WT), IL-23(-/-) or IL-17(-/-) mice using an elastase-perfusion model. Heat-inactivated elastase was used as control. On days 3, 7, and 14 after perfusion, abdominal aorta diameter was measured by video micrometry, and aortic tissue was analyzed for cytokines, cell counts, and IL-17-producing CD4+ T cells. Aortic diameter and cytokine production (MCP-1, RANTES, KC, TNF-α, MIP-1α, and IFN-γ) was significantly attenuated in elastase-perfused IL-17(-/-) and IL-23(-/-) mice compared with WT mice on day 14. Cellular infiltration (especially IL-17-producing CD4+ T cells) was significantly attenuated in elastase-perfused IL-17(-/-) mice compared with WT mice on day 14. Primary aortic smooth muscle cells were significantly activated by elastase or IL-17 treatment. Furthermore, MSC treatment significantly attenuated AAA formation and IL-17 production in elastase-perfused WT mice.

conclusionsThese results demonstrate that CD4+ T-cell-produced IL-17 plays a critical role in promoting inflammation during AAA formation and that immunomodulation of IL-17 by MSCs can offer protection against AAA formation.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsAortic Aneurysm, AbdominalCD4-Positive T-LymphocytesCrosses, GeneticCytokinesDisease Models, AnimalGene Expression RegulationHumansImmunomodulationInterleukin-17Interleukin-23 Subunit p19MaleMiceMice, Inbred C57BLMice, KnockoutCytokinesInterleukin-17Interleukin-23 Subunit p19Pancreatic Elastase

Identifiers

PMID22965992
PMCPMC3448933
OpenAlexW2142395364

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.