Evidence map›Paper›PMID 23835442›Full record

ArticleInflammatory bowel diseases2013

Alpha-1-antitrypsin therapy ameliorates acute colitis and chronic murine ileitis.

Colm B Collins, Carol M Aherne, Stefan F Ehrentraut, Mark E Gerich, Eóin N McNamee, Martine C McManus, Matthew D P Lebsack, Paul Jedlicka, Tania Azam, Edwin F de Zoeten and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Inflammatory bowel diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.8field-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

29 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Ceruletide and Alpha-1 Antitrypsin as a Novel Combination Therapy for Ischemic Stroke.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Article
  13. Article
  14. Digestive Inflammation: Role of Proteolytic Dysregulation.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Update on clinical and research application of fecal biomarkers for gastrointestinal diseases.World journal of gastrointestinal pharmacology and therapeutics · 2017
    Review
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

12 authors at 3 institutions in 1 country.

Colm B CollinsMucosal Inflammation Program, Division of Gastroenterology, University of Colorado School of Medicine, Aurora, Colorado, USA. colm.collins@ucdenver.edu
Carol M Aherne
Stefan F Ehrentraut
Mark E Gerich
Eóin N McNamee
Martine C McManus
Matthew D P Lebsack
Paul Jedlicka
Tania Azam
Edwin F de Zoeten
Charles A Dinarello
Jesús Rivera-Nieves
University of California, San Diego · USUniversity of Colorado Denver · USPediatrics and Genetics · US

Funding

Yeast-based HTS Assay Technologies for ProteasesR01AI015614 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DINARELLO, CHARLES ANTHONY · 1985 to 2025
$8.5M
Targeting L-Selectin in Chronic Murine IleitisR01DK080212 · NIDDK · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI RIVERA-NIEVES, JESUS · 2009 to 2013
$1.7M
Pathogenesis of Fever in ManR56AI015614 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DINARELLO, CHARLES ANTHONY · 2016 to 2016
$311k
Dendritic Cell Manipulation: A Novel Therapeutic for Inflammatory Bowel DiseaseI01BX001051 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI RIVERA-NIEVES, JESUS · 2011 to 2015
–
PATHOGENESIS OF FEVER IN HUMANSR37AI015614 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DINARELLO, CHARLES ANTHONY · 1988 to 1998
–
BLRD VA I01 BX001051NIAID NIH HHS AI-15614NIAID NIH HHS R01 AI015614NIAID NIH HHS R56 AI015614NIDDK NIH HHS DK080212-01NIDDK NIH HHS R01 DK080212
6 · The paper itself

Abstract

backgroundFecal alpha-1-antitrypsin (AAT) clearance has been a marker of clinical disease severity in inflammatory bowel diseases (IBDs) for many years. Although AAT deficiency is more often associated with lung and liver pathologies, AAT-deficient patients with concomitant IBD have been shown to develop more aggressive disease and rapid progression to surgery. Although recent studies have highlighted the pleiotropic anti-inflammatory functions of AAT, including reducing proinflammatory cytokine production and suppressing immune cell activation, its potential therapeutic role in IBD has not been described.

methodsThe therapeutic potential of human AAT administration was assessed in murine models of IBD including new-onset and established chemically induced colitis and spontaneous chronic murine ileitis. Histological assessment of inflammation, cytokine secretion profiling, and flow cytometric evaluation of inflammatory infiltrate were performed in each model. The effect of AAT on intestinal barrier function was also examined both in vitro and in vivo.

resultsAAT attenuated inflammation in small and large intestinal IBD models through reduced secretion of proinflammatory cytokines, inflammatory cell infiltration, and reduced tissue injury. AAT also increased intestinal restitution after chemically induced colitis. AAT significantly decreased intestinal permeability in vitro and in vivo as part of a protective mechanism for both acute and chronic models of IBD.

conclusionsOur findings describe a beneficial role for AAT in IBD models through suppression of cytokine production and enhanced intestinal barrier function. This raises the possibility that AAT supplementation, which has a long history of proven safety, may have a therapeutic effect in human IBD.

Indexed as

Acute Diseasealpha 1-AntitrypsinAnimalsCell Membrane PermeabilityChronic DiseaseColitisCytokinesDextran SulfateFlow CytometryHumansIleitisInflammationMicealpha 1-AntitrypsinCytokinesDextran SulfateSERPINA1 protein, human

Identifiers

PMID23835442
PMCPMC4654462
OpenAlexW1969730567

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.