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Immunological investigation in the adenoid tissues from children with chronic rhinosinusitis
Seung-Youp Shin1, Gil-Soon Choi, Hae-Sim Park
1Department of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, Kyunghee University, Seoul, Korea.
Insights
Pediatric chronic rhinosinusitis (CRS) is linked to increased tissue remodeling markers in adenoid tissues. These findings highlight the role of adenoid inflammation in pediatric CRS.
Area of Science:
- Immunology
- Otorhinolaryngology
- Pathology
Background:
- Chronic rhinosinusitis (CRS) involves persistent nasal inflammation and tissue remodeling.
- Adenoidectomy is a common surgical intervention for pediatric CRS.
- Understanding adenoid tissue changes in pediatric CRS is crucial for treatment.
Purpose of the Study:
- To investigate the impact of pediatric CRS on adenoid tissue inflammation.
- To quantify inflammatory cell activation markers and tissue remodeling cytokines in adenoid tissues of children with and without CRS.
- To correlate CRS severity with specific inflammatory markers.
Main Methods:
- A prospective controlled study involving 40 pediatric patients undergoing adenotonsillectomy.
- Immunoassays were performed on adenoid tissue homogenates from 16 children with CRS and 24 controls.
- Levels of soluble interleukin-2 receptor (sIL-2R), soluble CD23 (sCD23), IL-6, eosinophilic cationic protein (ECP), tryptase, transforming growth factor-beta1 (TGF-beta1), matrix metalloproteinase (MMP)-2, MMP-9, and tissue inhibitor of metalloproteinase (TIMP)-1 were measured.
Main Results:
- Significantly higher mean levels of sIL-2R, TGF-beta1, MMP-2, MMP-9, and TIMP-1 were observed in adenoid tissues of children with CRS compared to controls (P<0.05).
- Eosinophilic cationic protein (ECP) levels were significantly elevated in severe CRS cases compared to mild to moderate CRS (P=0.033).
- These findings indicate increased inflammatory cell activation and tissue remodeling in pediatric CRS.
Conclusions:
- Pediatric CRS is associated with elevated levels of tissue-remodeling-associated cytokines in adenoid tissues.
- These molecular changes may contribute to the observed adenoid inflammation in pediatric CRS.
- The study provides insights into thepathophysiology of pediatric CRS.
Objective:
Chronic rhinosinusitis (CRS) is characterized by persistent inflammation and tissue remodeling of the nasal mucosa. Adenoidectomy is an effective surgical treatment in pediatric CRS. To evaluate the effect of pediatric CRS on the severity and characteristics of adenoid inflammation, the authors evaluated the expressions of inflammatory cell activation markers and tissue remodeling in adenoid tissues associated with cytokines tissue-remodeling-associated cytokines in adenoid tissues.
Study Design And Setting:
A prospective controlled study on 40 pediatric patients admitting for adenotonsillectomy.
Subjects And Methods:
Immunoassays were performed on adenoid tissues homogenates from 16 children with CRS and from 24 children without CRS to quantify the levels of inflammatory cell activation markers, such as soluble interleukin (IL)-2 receptor (sIL-2R), soluble CD23 (sCD23), IL-6, eosinophilic cationic protein (ECP), and tryptase, and the levels of cytokines associated with tissue remodeling, such as transforming growth factor (TGF)-beta1, matrix metalloproteinase (MMP) 2 and 9, and tissue inhibitor of metalloproteinase (TIMP)-1.
Results:
The mean levels (the ratio to albumin level) of sIL-2R, TGF-beta1, MMP-2, MMP-9, and TIMP-1 were significantly higher in adenoid tissues of patients with CRS (27.31+/-30.32, 4894.65+/-2388.77, 500.13+/-604.59, and 23.06+/-10.37, respectively) than those without it (16.27+/-10.93, 2635.51+/-1448.63, 120.87+/-321.50, 16.74+/-11.10, and 7.39+/-3.12, respectively; all P<0.05). Regarding the severity of CRS, ECP level was significantly higher in patients with severe CRS than in those with mild to moderate CRS (P=0.033).
Conclusions:
Adenoid tissues in pediatric CRS patients had higher levels of tissue-remodeling-associated cytokines, which may explain the relationship between pediatric CRS and adenoid inflammation.
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