A Novel Insight into the Immunologic Basis of Chronic Granulomatous Invasive Fungal Rhinosinusitis

Author:

Rae William1,Doffinger Rainer23,Shelton Fenella4,Sproson Eleanor4,Ismail-Koch Hasnaa45,Lund Valerie J.6,Harries Philip G.4,Eren Efrem1,Salib Rami J.47

Affiliation:

1. Department of Immunology, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom

2. Department of Clinical Biochemistry and Immunology, Addenbrooke's Hospital, Cambridge, United Kingdom

3. National Institute for Health Research Cambridge Biomedical Research Centre, United Kingdom

4. Department of Otorhinolaryngology—Head and Neck Surgery, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom

5. Department of Otolaryngology, Southampton Children's Hospital, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom

6. Department of Otolaryngology, Royal National Throat, Nose and Ear Hospital, University College London, London, United Kingdom

7. Academic Unit of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom

Abstract

Background Chronic granulomatous invasive fungal rhinosinusitis (CGIFRS) is a rare disease. The underlying immune responses that drive the development of CGIFRS, as opposed to successful pathogen clearance and controlled inflammation, are not currently known. Objective To characterize the immune responses associated with CGIFRS. Methods In addition to a battery of basic investigations, more in-depth immunologic testing involves ex vivo whole-blood stimulation with the polyclonal T-cell mitogen phytohemagglutinin and fungal antigens with interleukin (IL) 12, was undertaken to investigate cell-mediated immune responses associated with CGIFRS. Results Ex vivo whole-blood stimulation with the polyclonal T-cell mitogen phytohemagglutinin and fungal antigens with IL-12 identified reduced interferon gamma and increased IL-17A levels within the supernatant, which indicated increased in vivo T-helper (Th)17 responses and impaired Th1 responses compared with healthy controls. Conclusion These findings suggest that the development of CGIFRS may be associated with an abnormally exaggerated host Th17 response, which caused failure to clear the fungal pathogen with refractory fungal infection of mucosal membranes, resulting in chronic tissue inflammation.

Publisher

SAGE Publications

Subject

Otorhinolaryngology,Immunology and Allergy

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