Evidence map›Paper›PMID 21701422›Full record

ArticleShock (Augusta, Ga.)2011

Epidermal growth factor improves survival and prevents intestinal injury in a murine model of pseudomonas aeruginosa pneumonia.

Jessica A Dominguez, Paul J Vithayathil, Ludmila Khailova, Christopher P Lawrance, Alexandr J Samocha, Enjae Jung, Ann M Leathersich, W Michael Dunne, Craig M Coopersmith

Open access · greenAbstract read
In one paragraph

Article in Shock (Augusta, Ga.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

38 citing papers in PubMed, 44 citations in OpenAlex.

  1. Sepsis and the diverse organ-gastrointestinal tract axis.World journal of critical care medicine · 2025
    Review
  2. Article
  3. Review
  4. Gut-derived immune cells and the gut-lung axis in ARDS.Critical care (London, England) · 2024
    Review
  5. Article
  6. Review
  7. Gut-liver crosstalk in sepsis-induced liver injury.Critical care (London, England) · 2020
    Review
  8. Article
  9. Esmolol inhibits inflammation and apoptosis in the intestinal tissue via the overexpression of NF-κB-p65 in the early stage sepsis rats.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2020
    Article
  10. Gut integrity in critical illness.Journal of intensive care · 2019
    Review
  11. Integrative Physiology of Pneumonia.Physiological reviews · 2018
    Review
  12. Gut-kidney crosstalk in septic acute kidney injury.Critical care (London, England) · 2018
    Review
  13. Article
  14. Sepsis reveals compartment-specific responses in intestinal proliferation and apoptosis in transgenic mice whose enterocytes re-enter the cell cycle.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  15. The intestinal microenvironment in sepsis.Biochimica et biophysica acta. Molecular basis of disease · 2017
    Review
  16. Article
  17. 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

9 authors at 3 institutions in 1 country.

Jessica A DominguezDepartment of Anesthesiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Paul J Vithayathil
Ludmila Khailova
Christopher P Lawrance
Alexandr J Samocha
Enjae Jung
Ann M Leathersich
W Michael Dunne
Craig M Coopersmith
Washington University in St. Louis · USUniversity of Colorado Anschutz Medical Campus · USEmory University · US

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
Mechanisms of Intestinal Integrity in Sepsis and ShockR01GM072808 · NIGMS · WASHINGTON UNIVERSITY · PI COOPERSMITH, CRAIG M · 2005 to 2021
$5.1M
Gut Epithelial Apoptosis in Shock and SepsisR01GM066202 · NIGMS · WASHINGTON UNIVERSITY · PI COOPERSMITH, CRAIG M · 2002 to 2010
$2.4M
POSTDOCTORAL TRAINING PROGRAM IN CRITICAL CARET32GM008795 · NIGMS · WASHINGTON UNIVERSITY · PI HOTCHKISS, RICHARD SAMUEL · 2001 to 2010
$1.6M
The Role of Epidermal Growth Factor in SepsisF32GM082008 · NIGMS · WASHINGTON UNIVERSITY · PI DOMINGUEZ RIEG, JESSICA A · 2008 to 2009
$57k
NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30 DK52574NIGMS NIH HHS F32 GM082008NIGMS NIH HHS GM008795NIGMS NIH HHS GM072808NIGMS NIH HHS GM082008NIGMS NIH HHS GM66202NIGMS NIH HHS R01 GM066202NIGMS NIH HHS R01 GM072808NIGMS NIH HHS T32 GM008795
6 · The paper itself

Abstract

Mortality from pneumonia is mediated, in part, through extrapulmonary causes. Epidermal growth factor (EGF) has broad cytoprotective effects, including potent restorative properties in the injured intestine. The purpose of this study was to determine the efficacy of EGF treatment following Pseudomonas aeruginosa pneumonia. FVB/N mice underwent intratracheal injection of either P. aeruginosa or saline and were then randomized to receive either systemic EGF or vehicle beginning immediately or 24 h after the onset of pneumonia. Systemic EGF decreased 7-day mortality from 65% to 10% when initiated immediately after the onset of pneumonia and to 27% when initiated 24 h after the onset of pneumonia. Even though injury in pneumonia is initiated in the lungs, the survival advantage conferred by EGF was not associated with improvements in pulmonary pathology. In contrast, EGF prevented intestinal injury by reversing pneumonia-induced increases in intestinal epithelial apoptosis and decreases in intestinal proliferation and villus length. Systemic cytokines and kidney and liver function were unaffected by EGF therapy, although EGF decreased pneumonia-induced splenocyte apoptosis. To determine whether the intestine was sufficient to account for extrapulmonary effects induced by EGF, a separate set of experiments was done using transgenic mice with enterocyte-specific overexpression of EGF (IFABP-EGF [intestinal fatty acid-binding protein linked to mouse EGF] mice), which were compared with wild-type mice subjected to pneumonia. IFABP-EGF mice had improved survival compared with wild-type mice following pneumonia (50% vs. 28%, respectively, P < 0.05) and were protected from pneumonia-induced intestinal injury. Thus, EGF may be a potential adjunctive therapy for pneumonia, mediated in part by its effects on the intestine.

Indexed as

AnimalsApoptosisDisease Models, AnimalEpidermal Growth FactorIntestinal DiseasesIntestinesMiceMice, TransgenicPeroxidasePneumoniaPseudomonas aeruginosaEpidermal Growth FactorPeroxidase

Identifiers

PMID21701422
PMCPMC3175258
OpenAlexW1991529207

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.