the presence of b7-h4+ macrophages and cd25+cd4+ and foxp3+ regulatory t cells in the microenvironment of nasal polyps – a preliminary report

Clicks: 180
ID: 180707
2010
Article Quality & Performance Metrics
Overall Quality Improving Quality
0.0 /100
Combines engagement data with AI-assessed academic quality
AI Quality Assessment
Not analyzed
Abstract
The nasal polyp (NP) seems to represent the end-stage of longstanding inflammation in patients with chronic rhinosinusitis.The aim of our study has been to evaluate the presence of two regulatory cell populations in the microenvironmentof NP: CD4+CD25high Foxp3+ (Treg) cells and B7-H4-expressing macrophages. Treg cells are actively able to inhibitT lymphocytes, while the population of B7-H4-expressing macrophages has recently been described as characterized bya regulatory function similar to that of Treg cells. For our study, we evaluated 14 NP tissue samples. The samples were dividedinto two main groups, eosinophilic (NP) and lymphocytic (NP), according to the predominant type of immune cell infiltration.The presence of Treg cells and B7-H4 positive macrophages in the samples was analyzed by FACS. Treg cells andB7-H4-expressing macrophages were identified in all the examined nasal polyps. The percentages of both Treg cells and ofB7H4 positive cells found in the eosinophilic nasal polyps were higher than those found in the lymphocytic nasal polyps.Treg cells and B7H4+ macrophage subpopulations were present in the NP microenvironment and the alterations in their percentageswere related to a distinct pattern of immune cell infiltration.
Reference Key
strek2010foliathe Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;P. Strek;R. Tomaszewska;A. Lazar;L. Wicherek;J. Kijowski;M. Dutsch-Wicherek;M. Majka
Journal reviews on recent clinical trials
Year 2010
DOI
DOI not found
URL
Keywords

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.