Literature DB >> 23172907

Pulse steroid therapy inhibits murine subglottic granulation.

Ankona Ghosh1, Genevieve Philiponis, Jennifer Y Lee, Kevin P Leahy, Sunil Singhal, Noam A Cohen, Natasha Mirza.   

Abstract

OBJECTIVE: Using a functional model of airway granulation tissue in subglottic stenosis, we investigated changes in inflammatory markers within granulation tissue in response to intraperitoneal dexamethasone injections. Changes in inflammatory markers will allow us to identify potential targets for immunological therapy. STUDY
DESIGN: Institutional Animal Care and Use Committee-approved animal study.
SETTING: Philadelphia Veterans Administration Medical Center animal research facility. SUBJECTS AND METHODS: Laryngotracheal complexes of donor mice underwent direct airway injury and were transplanted into subcutaneous tissue of 19 recipient mice in 2 groups: steroid treated and untreated, with sample sizes of 10 and 9, respectively. The steroid-treated arm received intraperitoneal injection of dexamethasone for 3 weeks. Laryngotracheal complexes were then harvested, and granulation formation was measured. The messenger RNA (mRNA) expression of transforming growth factor (TGF)-β(1) and interleukin (IL)-1 was quantified.
RESULTS: At 3 weeks posttransplantation, there were statistically significant differences in observable granulation formation as well as mRNA expression of TGF-β(1) and IL-1β in all groups within the steroid treated arm as compared with the untreated arm.
CONCLUSIONS: Systemic steroids have been used to prevent formation of granulation tissue and subglottic stenosis. However, the study of the immunologic markers and the corresponding changes with steroid treatment has not been well studied in animal models. Using a previously described novel murine model, we begin to delineate inflammatory markers that can be applied for potential therapeutic targets.

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Year:  2012        PMID: 23172907     DOI: 10.1177/0194599812466533

Source DB:  PubMed          Journal:  Otolaryngol Head Neck Surg        ISSN: 0194-5998            Impact factor:   3.497


  3 in total

1.  Rapamycin inhibits human laryngotracheal stenosis-derived fibroblast proliferation, metabolism, and function in vitro.

Authors:  Daryan R Namba; Garret Ma; Idris Samad; Dacheng Ding; Vinciya Pandian; Jonathan D Powell; Maureen R Horton; Alexander T Hillel
Journal:  Otolaryngol Head Neck Surg       Date:  2015-03-09       Impact factor: 3.497

2.  T-Helper 2 Lymphocyte Immunophenotype Is Associated With Iatrogenic Laryngotracheal Stenosis.

Authors:  Alexander T Hillel; Dacheng Ding; Idris Samad; Michael K Murphy; Kevin Motz
Journal:  Laryngoscope       Date:  2018-11-13       Impact factor: 3.325

3.  Persistent Inflammation and Nitric Oxide Dysregulation Are Transcriptomic Blueprints of Subglottic Stenosis.

Authors:  Hoang C B Nguyen; Tiffany N Chao; Noam A Cohen; Natasha Mirza
Journal:  Front Immunol       Date:  2021-12-20       Impact factor: 7.561

  3 in total

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