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(1-3)-β-D-Glucan vs Galactomannan Antigen in Diagnosing Invasive Fungal Infections (IFIs)
C Fontana1, R Gaziano, M Favaro
1Department of Experimental Medicine and Surgery, "Tor Vergata" University of Rome, Via Montpellier 1, 00133, Rome, Italy.
Abstract:
Invasive fungal infections (IFIs) are serious and often life-threatening complications in patients with haematological malignancies. Early diagnosis and the initiation of efficacious antifungal treatments could affect the prognosis of these patients. The detection of (1-3)-β-D-Glucan (BDG) could be a promising non-culture-based, noninvasive tool for IFI analyses in haemato-oncological patients, allowing the diagnosis of the two major IFIs, invasive aspergillosis (IA) and invasive candidiasis (IC), with a single test. The aim of this work was to evaluate and compare the use of the BDG in combination with the galactomannan antigen (GAL) assay in order to exclude or confirm suspected IFIs. Sera from 46 haemato-oncological patients (24 with proven/probable IFI and 22 without IFI symptoms) were evaluated retrospectively for the detection of GAL and BDG. In 24 patients, the serum BDG levels facilitated IFI diagnosis: 18 probable IA, 3 proven IA and 3 IC. In the remaining 22 patients, the BDG level helped exclude IFIs. The BDG was positive earlier than GAL in 5/24 cases [three of probable invasive aspergillosis (IA), one of proven IA and one case of proven invasive candidiasis (IC)] and was positive at the same time as GAL in 19/24 cases; in no case was GAL positive before BDG was. The BDG detection is useful, however, the test has a great limitation because it is a completely manual procedure.
Insights
The (1-3)-β-D-Glucan (BDG) test aids in diagnosing invasive fungal infections (IFIs) in cancer patients. BDG shows promise as a noninvasive tool, often detecting infections earlier than the galactomannan (GAL) assay.
Area of Science:
- Medical Mycology
- Clinical Diagnostics
- Hematology-Oncology
Background:
- Invasive fungal infections (IFIs) pose significant risks for patients with hematological malignancies.
- Early diagnosis and treatment are crucial for improving patient outcomes.
- Non-culture-based, noninvasive diagnostic tools are needed for timely IFI detection.
Purpose of the Study:
- To evaluate the utility of (1-3)-β-D-Glucan (BDG) in combination with galactomannan (GAL) assay for diagnosing IFIs in hemato-oncological patients.
- To compare the diagnostic performance and timing of BDG and GAL assays.
- To assess the role of BDG in excluding IFIs.
Main Methods:
- Retrospective analysis of serum samples from 46 hemato-oncological patients.
- Detection of (1-3)-β-D-Glucan (BDG) and galactomannan (GAL) antigen.
- Comparison of BDG and GAL results with proven/probable IFI status.
Main Results:
- BDG facilitated IFI diagnosis in 24 patients (18 probable IA, 3 proven IA, 3 IC).
- BDG helped exclude IFIs in 22 patients.
- BDG was positive earlier than GAL in 5 cases and concurrently in 19 cases; GAL was never positive before BDG.
Conclusions:
- Serum BDG is a valuable noninvasive marker for diagnosing invasive aspergillosis and invasive candidiasis in hemato-oncological patients.
- BDG can aid in the early detection and exclusion of IFIs.
- A significant limitation of the BDG assay is its entirely manual procedure.

