Evidence map›Paper›PMID 24670033›Full record

ReviewExpert opinion on therapeutic targets2014

Protein-based therapies for acute lung injury: targeting neutrophil extracellular traps.

Markus Bosmann, Peter A Ward

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. In-Depth Analysis ofBiology · 2024
    Article
  4. Article
  5. Neutrophil extracellular traps and pulmonary fibrosis: an update.Journal of inflammation (London, England) · 2023
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. [Monoclonal antibodies for anti-infective therapy].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2020
    Review
  12. Article
  13. Gut Microbiota Restricts NETosis in Acute Mesenteric Ischemia-Reperfusion Injury.Arteriosclerosis, thrombosis, and vascular biology · 2020
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Evidence for the important role of inflammation in xenotransplantation.Journal of inflammation (London, England) · 2019
    Review
  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

2 authors at 2 institutions in 2 countries.

Markus BosmannUniversity Medical Center, Center for Thrombosis and Hemostasis , Langenbeckstrasse 1, Mainz, 55131 , Germany +49 6131 17 8277 ; +49 6131 17 6238 ; markus.bosmann@unimedizin-mainz.demailto.
Peter A Ward
University Medical Center of the Johannes Gutenberg University Mainz · DEUniversity of Michigan–Ann Arbor · US

Funding

Regulation of Lung Inflammation by Catecholamines and Adrenergic ReceptorsR01GM029507 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WARD, PETER A · 1985 to 2013
$3.9M
Protective Effects of Anti-C5a in SepsisR01GM061656 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WARD, PETER A · 2002 to 2013
$3.8M
LUNG INJURY BY OXYGEN METABOLITESR37GM029507 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WARD, PETER A · 1987 to 1996
–
NIGMS NIH HHS GM-29507NIGMS NIH HHS GM-61656NIGMS NIH HHS R01 GM029507NIGMS NIH HHS R01 GM061656NIGMS NIH HHS R37 GM029507
6 · The paper itself

Abstract

introductionAcute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are the acute onset of noncardiac respiratory insufficiency associated with bilateral lung infiltrations. During the past decade, mechanical ventilation strategies using low tidal volumes have reduced the mortality of ALI/ARDS to ∼ 20 - 40%. However, ALI/ARDS continues to be a major factor in global burden of diseases, with no pharmacological agents currently available. AREAS COVERED: In this review, we discuss several inflammatory proteins involved in the molecular pathogenesis of ALI/ARDS. The complement cleavage product, C5a, is a peptide acting as a potent anaphylatoxin. C5a may trigger the formation of neutrophil extracellular traps (NETs) and release of histone proteins to the extracellular compartment during ALI/ARDS. NETs may activate platelets to release TGF-β, which is involved in tissue remodeling during the later phases of ALI/ARDS. Interception of C5a signaling or blockade of extracellular histones has recently shown promising beneficial effects in small animal models of ALI/ARDS. EXPERT OPINION: Novel protein-based strategies for the treatment of ALI/ARDS may inspire the hopes of scientists, clinicians, and patients. Although neutralization of extracellular histones/NETs, C5a, and TGF-β is effective in experimental models of ALI/ARDS, controlled clinical trials will be necessary for further evaluation in future.

Indexed as

Acute Lung InjuryAnimalsClinical Trials as TopicComplement C5aExtracellular TrapsHumansTransforming Growth Factor beta1Complement C5aTransforming Growth Factor beta1antibodyC5aextracellular histonesinflammationneutrophil extracellular trapsTGF-β

Identifiers

PMID24670033
PMCPMC4123211
OpenAlexW2080604579

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.