Fungi-Induced Upper and Lower Respiratory Tract Allergic Diseases: One Entity

Aleksandra Barac1,2, David S Y Ong3,4, Ljiljana Jovancevic5,6

  • 1Clinic for Infectious and Tropical Diseases, Clinical Centre of Serbia, Belgrade, Serbia.

Insights

Allergic fungal rhinosinusitis (AFRS) is present in 80% of patients with allergic bronchopulmonary aspergillosis (ABPA), suggesting a common fungal-induced allergic airway disease entity. Further research is needed to understand fungal triggers and improve diagnosis and treatment.

Area of Science:

  • Allergy and Immunology
  • Pulmonology
  • Otolaryngology

Background:

  • Allergic bronchopulmonary aspergillosis (ABPA) is a pulmonary allergic disease caused by Aspergillus antigens.
  • Allergic fungal rhinosinusitis (AFRS) involves hypersensitivity reactions to fungi in the sinuses, often presenting as chronic rhinosinusitis (CRS).

Purpose of the Study:

  • To investigate whether ABPA and AFRS represent a common disease entity.
  • To compare clinical and mycological findings between ABPA patients with and without co-existing AFRS.

Main Methods:

  • A prospective cohort study of 75 ABPA patients.
  • Patients were categorized into two groups: ABPA with confirmed AFRS (CT and fungal evidence) and ABPA without AFRS.
  • Comparison of sinonasal findings, allergy testing, and home air sampling between groups.

Main Results:

  • AFRS was confirmed in 80% of ABPA patients, with allergic mucin present in all.
  • Fungal hyphae were found in 60% of sinonasal aspirates, and cultures revealed fungal presence in 97% of the ABPA+AFRS group.
  • ABPA+AFRS patients exhibited higher rates of complicated CRS, nasal polyps, positive skin prick tests for Aspergillus fumigatus, and higher fungal loads in home air samples.

Conclusions:

  • AFRS is the upper airway manifestation of ABPA, indicating a shared pathogenesis in fungi-induced allergic upper and lower respiratory diseases.
  • The findings support considering ABPA and AFRS as a common disease entity.
  • Further research is required to elucidate the mechanisms of fungal immune triggers and develop novel diagnostic and therapeutic strategies.

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