Evidence map›Paper›PMID 25006447›Full record

ArticlePulmonary circulation2014

Pleiotropic effects of interleukin-6 in a "two-hit" murine model of acute respiratory distress syndrome.

Julia L Goldman, Saad Sammani, Carrie Kempf, Laleh Saadat, Eleftheria Letsiou, Ting Wang, Liliana Moreno-Vinasco, Alicia N Rizzo, Jeffrey D Fortman, Joe G N Garcia

Abstract read
In one paragraph

Article in Pulmonary circulation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
5.6field-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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. TLR7 Mediates Acute Respiratory Distress Syndrome in Sepsis by Sensing Extracellular miR-146a.American journal of respiratory cell and molecular biology · 2022
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. IL-6 Inhibition Reduces Neuronal Injury in a Murine Model of Ventilator-induced Lung Injury.American journal of respiratory cell and molecular biology · 2021
    Article
  16. Article
  17. Strategies to DAMPen COVID-19-mediated lung and systemic inflammation and vascular injury.Translational research : the journal of laboratory and clinical medicine · 2021
    Review
  18. Observational
  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

10 authors at 1 institution in 1 country.

Julia L GoldmanInstitute of Personalized Respiratory Medicine, University of Illinois at Chicago, Chicago, Illinois, USA ; Biological Resources Laboratory, University of Illinois at Chicago, Chicago, Illinois, USA.
Saad SammaniInstitute of Personalized Respiratory Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Carrie KempfInstitute of Personalized Respiratory Medicine, University of Illinois at Chicago, Chicago, Illinois, USA ; Current affiliation: Division of Pulmonary and Critical Care, Sleep Medicine, Arizona Respiratory Center, University of Arizona, Tucson, Arizona, USA.
Laleh SaadatInstitute of Personalized Respiratory Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Eleftheria LetsiouInstitute of Personalized Respiratory Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Ting WangInstitute of Personalized Respiratory Medicine, University of Illinois at Chicago, Chicago, Illinois, USA ; Current affiliation: Division of Pulmonary and Critical Care, Sleep Medicine, Arizona Respiratory Center, University of Arizona, Tucson, Arizona, USA.
Liliana Moreno-VinascoInstitute of Personalized Respiratory Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Alicia N RizzoInstitute of Personalized Respiratory Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Jeffrey D FortmanBiological Resources Laboratory, University of Illinois at Chicago, Chicago, Illinois, USA.
Joe G N GarciaInstitute of Personalized Respiratory Medicine, University of Illinois at Chicago, Chicago, Illinois, USA ; Office of the Vice President for Health Affairs, University of Illinois at Chicago, Chicago, Illinois, USA ; Current affiliation: Division of Pulmonary and Critical Care, Sleep Medicine, Arizona Respiratory Center, University of Arizona, Tucson, Arizona, USA.
University of Illinois Chicago · US

Funding

Tissue Culture Biomechanical CoreP01HL058064 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LAL, RATNESHWAR · 1998 to 2012
$27.8M
Structure-Function Analysis of nmMLCK in EC Barrier ResponsesP01HL126609 · NHLBI · UNIVERSITY OF FLORIDA · PI STEVEN M DUDEK · 2016 to 2026
$24.4M
NHLBI NIH HHS P01 HL058064NHLBI NIH HHS P01 HL126609
6 · The paper itself

Abstract

Patients with acute respiratory distress syndrome (ARDS) exhibit elevated levels of interleukin-6 (IL-6), which correlate with increased morbidity and mortality. The exact role of IL-6 in ARDS has proven difficult to study because it exhibits either pro- or anti-inflammatory actions in mouse models of lung injury, depending on the model utilized. In order to improve understanding of the role of this complex cytokine in ARDS, we evaluated IL-6 using the clinically relevant combination of lipopolysaccharide (LPS) and ventilator-induced lung injury (VILI) in IL-6(-/-) mice. Bronchoalveolar lavage fluid (BAL), whole-lung tissue, and histology were evaluated for inflammatory markers of injury. Transendothelial electrical resistance was used to evaluate the action of IL-6 on endothelial cells in vitro. In wild-type mice, the combination model showed a significant increase in lung injury compared to either LPS or VILI alone. IL-6(-/-) mice exhibited a statistically significant decrease in BAL cellular inflammation as well as lower histologic scores for lung injury, changes observed only in the combination model. A paradoxical increase in BAL total protein was observed in IL-6(-/-) mice exposed to LPS, suggesting that IL-6 provides protection from vascular leakage. However, in vitro data showed that IL-6, when combined with its soluble receptor, actually caused a significant increase in endothelial cell permeability, suggesting that the protection seen in vivo was likely due to complex interactions of IL-6 and other inflammatory mediators rather than to direct effects of IL-6. These studies suggest that a dual-injury model exhibits utility in evaluating the pleiotropic effects of IL-6 in ARDS on inflammatory cells and lung endothelium.

Indexed as

acute respiratory distress syndrome (ARDS)interleukin-6 (IL-6)lipopolysaccharide (LPS)ventilator-induced lung injury (VILI)

Identifiers

PMID25006447
PMCPMC4070787
OpenAlexW1984705347

What OpenQuestion holds

Textmetadata
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.