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Updated: Aug 11, 2026

Detection of Invasive Pulmonary Aspergillosis in Haematological Malignancy Patients by using Lateral-flow Technology
Published on: March 22, 2012
Rapid diagnosis of candidiasis and aspergillosis
Abstract:
Published studies support the hypothesis that at least two antigens of Candida albicans and Candida tropicalis circulate in the bloodstream of patients with severe candidiasis. One antigen (probably mannan) is stable and the other (probably protein) is labile. The stabile antigen can rarely be detected without prior dissociation from antibody. Dissociation treatment destroys the labile antigen, leaving in doubt whether any is antibody bound. Dissociation steps have also been necessary for detection of Aspergillus fumigatus antigen in sera from patients with invasive aspergillosis. Concentrations of the stable antigens of both Candida and Aspergillus appear to be in the nanogram-per-milliliter range, generally lying at the limits of detection by conventional assays. Improvements in sensitivity and practicality are needed, but the tests are clearly promising.
Insights
Detecting fungal antigens in severe candidiasis patients shows promise. Stable Candida and Aspergillus antigens are detectable in blood, though detection methods need improvement for better sensitivity.
Area of Science:
- Mycology
- Clinical Microbiology
- Immunodiagnostics
Background:
- Severe candidiasis involves bloodstream infections by Candida species.
- Circulating fungal antigens are potential biomarkers for invasive fungal infections.
- Previous studies suggest the presence of both stable and labile antigens in candidiasis.
Purpose of the Study:
- To evaluate the presence and detectability of circulating fungal antigens in patients with severe candidiasis.
- To assess the characteristics of stable and labile antigens from Candida albicans and Candida tropicalis.
- To explore the utility of antigen detection for diagnosing invasive aspergillosis.
Main Methods:
- Analysis of patient sera for fungal antigens using dissociation techniques.
- Characterization of antigen stability (stable vs. labile) and antibody binding.
- Quantification of antigen concentrations in the nanogram-per-milliliter range.
Main Results:
- Two types of circulating antigens (stable and labile) were supported in severe candidiasis.
- Stable antigens required dissociation from antibodies for detection.
- Dissociation destroyed labile antigens, complicating assessment of antibody-bound forms.
- Similar dissociation steps were needed for Aspergillus fumigatus antigen detection.
- Stable antigen concentrations were in the nanogram-per-milliliter range, near assay detection limits.
Conclusions:
- Circulating stable antigens of Candida and Aspergillus are detectable in patients with invasive infections.
- Current detection assays for these fungal antigens have limitations in sensitivity and practicality.
- Further improvements in diagnostic assays are needed, but antigen detection shows diagnostic potential.
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