Evidence map›Paper›PMID 37811005›Full record

ArticleCellular and molecular bioengineering2023

Amelioration of Subglottic Stenosis by Antimicrobial Peptide Eluting Endotracheal Tubes.

Matthew R Aronson, Amrita Mehta, Ryan M Friedman, Daniel D Ghaderi, Ryan C Borek, Hoang C B Nguyen, Kendra S McDaid, Ian N Jacobs, Natasha Mirza, Riccardo Gottardi

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Inhibition of the MRTF-A/SRF signaling axis alleviates vocal fold scarring.Matrix biology : journal of the International Society for Matrix Biology · 2025
    Article
  2. Review
  3. Microbiome and Communication Disorders: A Tutorial for Clinicians.Journal of speech, language, and hearing research : JSLHR · 2025
    Review
  4. Article
  5. 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 2 institutions in 2 countries.

Matthew R AronsonDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA USA.ORCID 0000-0002-8871-8265
Amrita MehtaDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA USA.
Ryan M FriedmanDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA USA.
Daniel D GhaderiDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA USA.
Ryan C BorekDivision of Otolaryngology, Department of Surgery, Children's Hospital of Philadelphia, Philadelphia, PA USA.
Hoang C B NguyenDivision of Otolaryngology, Philadelphia Veterans Affairs Medical Center, Philadelphia, PA USA.
Kendra S McDaidDepartment of Laboratory Animal Services, The Children's Hospital of Philadelphia, Philadelphia, PA USA.
Ian N JacobsDivision of Otolaryngology, Department of Surgery, Children's Hospital of Philadelphia, Philadelphia, PA USA.
Natasha MirzaDivision of Otolaryngology, Philadelphia Veterans Affairs Medical Center, Philadelphia, PA USA.
Riccardo GottardiDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA USA.ORCID 0000-0001-8040-5531
Children's Hospital of Philadelphia · USHospital of the University of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Pediatric subglottic stenosis (SGS) results from prolonged intubation where scar tissue leads to airway narrowing that requires invasive surgery. We have recently discovered that modulating the laryngotracheal microbiome can prevent SGS. Herein, we show how our patent-pending antimicrobial peptide-eluting endotracheal tube (AMP-ET) effectively modulates the local airway microbiota resulting in reduced inflammation and stenosis resolution. Materials and Methods: We fabricated mouse-sized ETs coated with a polymeric AMP-eluting layer, quantified AMP release over 10 days, and validated bactericidal activity for both planktonic and biofilm-resident bacteria against Results: We achieved reproducible, linear AMP release at 1.16 µg/day resulting in strong bacterial inhibition in vitro and ex vivo. In vivo, SGS-induced LTCs exhibited a thickened scar tissue typical of stenosis, while the use of AMP-ETs abrogated stenosis. Notably, SGS airways exhibited high infiltration of T cells and macrophages, which was reversed with AMP-ET treatment. This suggests that by modulating the microbiome, AMP-ETs reduce macrophage activation and antigen specific T cell responses resolving stenosis progression. Conclusion: We developed an AMP-ET platform that reduces T cell and macrophage responses and reduces SGS in vivo via airway microbiome modulation. Supplementary Information: The online version contains supplementary material available at 10.1007/s12195-023-00769-9.

Indexed as

Controlled drug deliveryImmunomodulatory biomaterialsPediatricsUpper airway disease

Identifiers

PMID37811005
PMCPMC10550884
OpenAlexW4382539091

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.