Allergic fungal rhinosinusitis

Mark S Dykewicz1, Jonathan M Rodrigues2, Raymond G Slavin1

  • 1Section of Allergy and Immunology, Division of Infectious Diseases, Allergy and Immunology, Department of Internal Medicine, Saint Louis University School of Medicine, St Louis, Mo.

Insights

Allergic fungal rhinosinusitis (AFRS) involves fungal sensitivity and allergic mucin in sinus inflammation. Treatment primarily requires surgery, with corticosteroids aiding recurrence prevention, while other therapies lack strong evidence.

Area of Science:

  • Immunology
  • Otolaryngology
  • Allergy

Background:

  • Allergic fungal rhinosinusitis (AFRS) is a specific type of chronic rhinosinusitis with nasal polyps (CRSwNP).
  • It is defined by IgE sensitivity to fungi, eosinophilic allergic mucin, and distinct sinus imaging findings.
  • AFRS occurs in immunocompetent individuals, influenced by environmental and host factors.

Purpose of the Study:

  • To delineate the molecular pathways and immune responses underlying AFRS.
  • To investigate if AFRS represents an extreme form of CRSwNP pathways or a distinct endotype.
  • To review current treatment strategies and identify areas for future research.

Main Methods:

  • Review of existing literature on AFRS pathophysiology and immune mechanisms.
  • Comparison of immune responses in AFRS with other CRSwNP and allergic conditions.
  • Analysis of current treatment modalities, including surgical and pharmacological interventions.

Main Results:

  • AFRS involves adaptive and innate type 2 immune responses, similar to CRSwNP.
  • The precise immune endotype of AFRS remains to be fully elucidated.
  • Surgical debridement is the primary treatment; oral corticosteroids help prevent recurrence.

Conclusions:

  • AFRS shares immune pathways with CRSwNP, but distinct endotypes may exist.
  • Adjunctive therapies like antifungals lack strong evidence; biologics targeting type 2 inflammation warrant investigation.
  • Further research is needed to confirm the efficacy of biologic agents in AFRS patients.

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