CCAD or eCRS: Defining Eosinophilic Subpopulations in Chronic Rhinosinusitis

Author:

Sit Andrea12ORCID,Alvarado Raquel1,Earls Peter13,Rimmer Janet145,Kalish Larry167,Campbell Raewyn189,Sewell William210ORCID,Harvey Richard J.19

Affiliation:

1. Rhinology and Skull Base Research Group, St Vincent's Centre for Applied Medical Research, Sydney, New South Wales, Australia

2. St Vincent's Clinical School, University of New South Wales, Sydney, Australia

3. Department of Anatomical Pathology, St Vincent's Hospital, Sydney, Australia

4. Woolcock Institute, University of Sydney, Sydney, Australia

5. Faculty of Medicine, Notre Dame University, Sydney, Australia

6. Faculty of Medicine, University of Sydney, Sydney, Australia

7. Department of Otolaryngology, Head and Neck Surgery, Concord General Hospital, Sydney, Australia

8. Department of Otolaryngology, Head and Neck Surgery, Royal Prince Alfred Hospital, Sydney, Australia

9. Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, Australia

10. Immunology Division, Garvan Institute, Sydney, Australia

Abstract

Background Central compartment atopic disease (CCAD) and eosinophilic chronic rhinosinusitis (eCRS) are two clinical phenotypes of primary diffuse type 2 chronic rhinosinusitis (CRS) defined in the European Position Paper on Rhinosinusitis 2020 classification. Currently, the distinction between these subtypes relies on phenotypic features alone. Objective This study aimed to investigate whether eosinophil activation differed between CCAD and eCRS. Methods A cross-sectional study was conducted of adult patients presenting with CCAD and eCRS who had undergone functional endoscopic sinus surgery. Routine pathology results were obtained from clinical records. Eosinophils were counted on haematoxylin and eosin-stained formalin-fixed paraffin-embedded sinonasal tissue. Eotaxin-3, eosinophil peroxidase and immunoglobulin E levels were assessed using immunohistochemistry. Results 38 participants were included (51.7 ± 15.6 years, 47.4% female), of whom 36.8% were diagnosed with CCAD and 63.2% with eCRS. The eCRS group was characterised by older age (55.8 ± 16.3 vs 44.5 ± 11.8 years, p = 0.029), and on histology exhibited a higher degree of tissue inflammation ( τb = 0.409, p = 0.011), greater proportion of patients with >100 eosinophils/high power field (87.5% vs 50%, p = 0.011), and higher absolute tissue eosinophil count (2141 ± 1947 vs 746 ± 519 cells/mm2, p = 0.013). Eotaxin-3 scores were higher in the eCRS group (5.00[5.00–6.00] vs 6.00[6.00–6.75], p  = 0.015). Other outcomes were similar. Conclusions Eosinophil and eotaxin-3 levels were elevated in eCRS compared with CCAD, suggesting a greater degree of eosinophil stimulation and chemotaxis. Patients with CCAD were younger. Future investigation and biomarkers may better distinguish CRS subpopulations.

Publisher

SAGE Publications

Subject

General Medicine,Otorhinolaryngology,Immunology and Allergy

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