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Examining the Role of Nasopharyngeal-associated Lymphoreticular Tissue NALT in Mouse Responses to Vaccines
Published on: August 1, 2012
Lymphocytes and nonlymphoid cells in human nasal polyps
A E Stoop1, H A van der Heijden, J Biewenga
1Department of Otorhinolaryngology/Head and Neck Surgery, Free University Hospital, Amsterdam, The Netherlands.
Insights
Nasal polyps show a higher concentration of CD8+ T-cells compared to CD4+ T-cells, indicating a role for T-cell disturbances in chronic inflammation and polyp development.
Area of Science:
- Immunology
- Otorhinolaryngology
- Pathology
Background:
- Nasal polyps are associated with chronic inflammation.
- The specific immune cell profiles in nasal polyps and surrounding tissues require further elucidation.
Purpose of the Study:
- To investigate the cellular composition of nasal polyps and compare it with unaffected nasal mucosa.
- To explore the potential role of immune cell disturbances in the pathogenesis of nasal polyps.
Main Methods:
- Immunohistochemical staining was performed on nasal polyp specimens (n=48) and mucosal biopsies from middle (n=23) and inferior turbinates (n=28).
- Quantification of various immune cells including T-lymphocytes (CD2+, CD4+, CD8+), B-cells (CD22+), HLA-DR+ cells, eosinophils, mast cells, plasma cells, and neutrophils.
Main Results:
- Nasal polyps exhibited significantly more CD8+ (suppressor/cytotoxic) than CD4+ (helper/inducer) T-cells.
- Immune cell counts in polyps were similar to middle turbinate mucosa but higher than inferior turbinates.
- Eosinophils were abundant in 77% of polyps, with moderate numbers of mast cells, plasma cells, and neutrophils.
Conclusions:
- The findings suggest a T-cell-dependent inflammatory process in nasal polyp pathogenesis.
- Disturbances in T-cell populations may contribute to the chronic inflammation observed in nasal polyps.
Abstract:
Immunohistochemical stainings were performed on polyp specimens of 48 patients and on mucosal biopsy specimens of the middle and inferior turbinates of 23 and 28 patients, respectively. Significantly more CD8+ (suppressor/cytotoxic) than CD4+ (helper/inducer) cells were found in the polyps. The number of CD2+, CD4+, and CD8+ lymphocytes in nasal polyps were very similar to the number in the macroscopically unaffected mucosa of the middle turbinates, whereas scores in the inferior turbinates were lower. In healthy subjects, the differences were smaller. CD22+ B cells were detected in varying numbers in the polyps in more or less organized clusters. Significantly more HLA-DR+ cells were found in polyps and middle turbinates than in the inferior turbinates. Eosinophils were found in moderate to large numbers in polyps of 77% of the patients. Mast cells and plasma cells were detected in moderate numbers, whereas neutrophils were found in 35% of the patients. In the middle and inferior turbinates varying but small numbers of eosinophils, mast cells, plasma cells, and neutrophils were found. In considering these findings, the role of chronic inflammation with T cell-dependent disturbances is discussed with regard to the pathogenesis of nasal polyps.
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