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Allergic fungal airway disease: pathophysiologic and diagnostic considerations
Kerry Woolnough1, Abbie Fairs, Catherine H Pashley
1aInstitute for Lung Health, Department of Infection Immunity and Inflammation, University of Leicester bDepartment of Allergy and Respiratory Medicine, University Hospitals of Leicester NHS Trust, Leicester, UK.
Purpose Of Review:
Fungal spores are ubiquitously present in indoor and outdoor air. A number can act as aeroallergens in Immunoglobulin E (IgE)-sensitized individuals and some thermotolerant fungi germinate in the lung where they can cause a combined allergic and infective stimulus leading to a number of clinical presentations characterized by evidence of lung damage. We discuss which biomarkers are useful in helping to guide diagnosis, prognosis and treatment of allergic fungal airway disease (AFAD).
Recent Findings:
Diagnostic biomarkers, such as specific IgEs and fungal culture, for AFAD are limited by sensitivity, although this may be improved with novel agents such as specific IgEs to fungal components and quantitative PCR. Total IgE and hypereosinophilia are nonspecific and do not clearly relate to disease activity. High attenuation mucus and proximal bronchiectasis are specific, albeit insensitive markers of AFAD. Biomarkers that predict prognosis and treatment response are yet to be defined.
Summary:
This review summarizes the fungi involved and the current debate regarding the diagnostic criteria to define fungal-associated lung disease. We advocate the phasing out of the term allergic bronchopulmonary aspergillosis and the use of a more inclusive term such as AFAD, together with a more liberal set of criteria based largely on IgE sensitization to thermotolerant fungi, which identifies those patients at risk of developing lung damage.
Insights
Allergic fungal airway disease (AFAD) diagnosis requires better biomarkers. Current methods like IgE tests lack sensitivity, but new techniques show promise for identifying patients at risk of lung damage.
Area of Science:
- Medical Mycology
- Pulmonology
- Allergy and Immunology
Background:
- Fungal spores are common airborne allergens.
- Some fungi can cause both allergic and infectious lung responses.
- Thermotolerant fungi pose a risk for lung damage in sensitized individuals.
Purpose of the Study:
- To review biomarkers for diagnosing, predicting prognosis, and guiding treatment of allergic fungal airway disease (AFAD).
- To discuss current diagnostic criteria and propose a more inclusive term (AFAD) for fungal-associated lung disease.
Main Methods:
- Review of current literature on fungal spores, aeroallergens, and lung disease.
- Analysis of diagnostic biomarkers including specific IgEs, fungal culture, quantitative PCR, total IgE, hypereosinophilia, high attenuation mucus, and bronchiectasis.
- Discussion of clinical presentations and diagnostic criteria for fungal-associated lung disease.
Main Results:
- Current diagnostic biomarkers for AFAD, such as specific IgEs and fungal cultures, have limited sensitivity.
- Novel biomarkers like specific IgEs to fungal components and quantitative PCR may improve sensitivity.
- Non-specific markers like total IgE and hypereosinophilia do not correlate well with disease activity; high attenuation mucus and bronchiectasis are specific but insensitive markers.
Conclusions:
- The term allergic bronchopulmonary aspergillosis should be replaced with the more inclusive term allergic fungal airway disease (AFAD).
- Liberalized diagnostic criteria focusing on IgE sensitization to thermotolerant fungi are recommended.
- These criteria can help identify patients susceptible to developing lung damage from fungal exposure.
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