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Updated: Feb 15, 2026

Measuring Mitochondrial Function of Naïve and Effector CD8 T Cells
Published on: March 28, 2025
Naive and effector B-cell subtypes are increased in chronic rhinosinusitis with polyps
Dijana Miljkovic1, Alkis Psaltis1, Peter-John Wormald1
1From the Department of Surgery-Otolaryngology Head and Neck Surgery, University of Adelaide, Adelaide, South Australia, Australia.
Patients with chronic rhinosinusitis with nasal polyposis (CRSwNP) show elevated B cells in nasal tissue, including naive, plasmablast, and memory B-cell subsets. These findings suggest a role for mucosal B cells in CRSwNP inflammation.
Area of Science:
- Immunology
- Otorhinolaryngology
- Cell Biology
Background:
- Chronic rhinosinusitis with nasal polyposis (CRSwNP) is associated with elevated B cells and chemoattractants in nasal mucosa.
- Previous research has not fully characterized naive, plasmablast, and memory B-cell subsets in CRSwNP mucosa and periphery.
Purpose of the Study:
- To quantify naive, plasmablast, and memory B cells in mucosal tissue and peripheral blood.
- To compare B-cell subset frequencies in patients with CRSwNP, CRS without nasal polyps (CRSsNP), and healthy controls.
Main Methods:
- Prospective collection of polyp, mucosa, and peripheral blood samples from CRS patients and controls.
- Flow cytometry was utilized to differentiate and quantify naive, plasmablast, and memory B-cell populations in sinus tissue and blood.
Main Results:
- CRSwNP patients exhibited significantly higher mucosal B-cell numbers compared to controls (p < 0.01).
- Elevated frequencies of naive B cells (p < 0.03), plasmablasts (p < 0.055), and memory B cells (p < 0.02) were observed in CRSwNP mucosa.
- No significant differences in peripheral blood B-cell subsets were found between groups.
Conclusions:
- Increased frequencies of various B-cell subtypes are present in the mucosa of CRSwNP patients.
- These mucosal B-cell increases were significantly higher in CRSwNP patients compared to CRSsNP patients and controls.
- These findings suggest a potential role for mucosal B cells in the inflammatory processes of CRSwNP.
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