Diagnosis of invasive aspergillosis remains difficult, and is often based on a combination of patient characteristics, radiological and microbiological findings. To data, galactomannan (GM) is the only well-validated biomarker available. However, GM still has its shortcomings. There is therefore a need for new, complementary biomarkers. In this study, two of those tests, bis(methylthio)gliotoxin (bmGT) and a lateral flow device, will be validated in a hematological population, and compare it to GM.
Diagnosis of invasive aspergillosis is often difficult to achieve with certainty, as this requires direct evidence of invasive growth on histopathological examination. A probable diagnosis can be suspected based on both clinical and mycological evidence of the disease, in presence of a susceptible patient. The EORTC-MSG guidelines offer a widely accepted basis for this diagnosis. Under these guidelines, mycological evidence can consist of a positive culture of aspergillus spp, or of detection of galactomannan (GM) in a relevant body sample. GM is a part of the Aspergillus mould and can be detected using a commercially available immunoenzymatic sandwich microplate assay. However, like most biomarkers, galactomannan is far from a perfect biomarker. Several beta-lactam antibiotics are known to cause false positives, and anti-mould therapy has been reported to significantly lower the sensitivity\[1\]. Additional biomarkers that could circumvent these problems would therefore be beneficial. A potential new target is gliotoxin (GT), a secondary metabolite of several fungi, the most clinically important of which is Aspergillus\[2\]. GT is released during invasive growth, and can therefore be used as a biomarker of invasive fungal disease by GT-producing fungi. However, GT is quickly removed by red blood cells from circulation, making it an unreliable marker\[3\]. A degradation product of GT, bis(methylthio)gliotoxin (bmGT), appears to be more stable as it is not taken up by red blood cells. Serum bmGT or bmGT in bronchoalveolar lavage (BAL) fluid has already been shown in small studies to be a potential marker of invasive aspergillosis, especially when used in combination with GM\[3-5\]. Recently, another highly specific test has become available, based on detection of an extracellular glycoprotein secreted during the growth of Aspergillus species, using a monoclonal antibody (JF5) in an immunochromatographic lateral-flow device (LFD)\[6,7\]. This test allows fast (\<15 minutes) testing using a commercially available device. In this study, both the LFD and bmGT will be characterized and validated in a hematological population, and compared to GM.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
226
Twice weekly blood sample, and at every outpatient visit
University Hospitals Leuven
Leuven, Belgium
Diagnostic accuracy of serum bmGT
Determine the diagnostic accuracy (specificity, sensitivity predictive values, accuracy and other key diagnostic values) of serum bmGT in the diagnosis of invasive aspergillosis, using the revised EORTC criteria as gold standard.
Time frame: 2 weeks
Diagnostic accuracy of a combination of serum bmGT and serum GM
Determine diagnostic accuracy of a combination of serum GM and serum bmGT in the diagnosis of invasive aspergillosis.
Time frame: 2 weeks
Prognostic value of serum bmGT
Determine prognostic value (therapy response / mortality) of initial serum bmGT levels.
Time frame: 6 weeks
Prognostic value of serum bmGT kinetics
Evaluate serum bmGT kinetics as surrogate marker of therapeutic response.
Time frame: 6 weeks
Renal and hepatic influence on bmGT
Evaluate the impact of renal and hepatic function on initial bmGT levels and bmGT kinetics.
Time frame: 2 weeks
Compare bmGT-HPTLC to bmGT-LC/MS
Compare bmGT levels as measured by HPTLC to levels as measured by our own in-house developed chromatographic method.
Time frame: Same day
Diagnostic accuracy of BAL bmGT
Determine diagnostic accuracy of bmGT in BAL in the diagnosis of invasive aspergillosis.
Time frame: 2 weeks
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Diagnostic accuracy of LFD
Determine diagnostic accuracy of the lateral flow device (LFD) in BAL and serum in the diagnosis of invasive aspergillosis.
Time frame: 2 weeks