Distinguishing Invasive from Chronic Pulmonary Infections: Host Pentraxin 3 and Fungal Siderophores in Bronchoalveolar Lavage Fluids

. 2022 Nov 12 ; 8 (11) : . [epub] 20221112

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid36422015

Grantová podpora
21-17044S Grant Agency of Czech Republic
SGS01-2021 Internal Grant Agency of University of Ostrava
CZ.02.1.01/0.0/0.0/16_025/000739 Ministry of Education, Youth and Sport of the Czech Republic

The multiple forms of pulmonary aspergillosis caused by Aspergillus species are the most common respiratory mycoses. Although invasive, the analysis of diagnostic biomarkers in bronchoalveolar lavage fluid (BALF) is a clinical standard for diagnosing these conditions. The BALF samples from 22 patients with proven or probable aspergillosis were assayed for human pentraxin 3 (Ptx3), fungal ferricrocin (Fc), and triacetylfusarinine C (TafC) in a retrospective study. The infected group included patients with invasive pulmonary aspergillosis (IPA) and chronic aspergillosis (CPA). The BALF data were compared to a control cohort of 67 patients with invasive pulmonary mucormycosis (IPM), non-Aspergillus colonization, or bacterial infections. The median Ptx3 concentrations in patients with and without aspergillosis were 4545.5 and 242.0 pg/mL, respectively (95% CI, p < 0.05). The optimum Ptx3 cutoff for IPA was 2545 pg/mL, giving a sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of 100, 98, 95, and 100%, respectively. The median Ptx3 concentration for IPM was high at 4326 pg/mL. Pentraxin 3 assay alone can distinguish IPA from CPA and invasive fungal disease from colonization. Combining Ptx3 and TafC assays enabled the diagnostic discrimination of IPM and IPA, giving a specificity and PPV of 100%.

California Institute for Medical Research 2260 Clove Dr San Jose CA 95128 USA

Department of Analytical Chemistry Faculty of Science Palacký University 77146 Olomouc Czech Republic

Department of Anesthesiology and Intensive Care Medicine University Hospital Ostrava 70800 Ostrava Czech Republic

Department of Bacteriology and Mycology National Reference Laboratory for Mycological Diagnostics Public Health Institute in Ostrava 70200 Ostrava Czech Republic

Department of Biology and Ecology Faculty of Science University of Ostrava 71000 Ostrava Czech Republic

Department of Clinical Biochemistry AGEL Hornická poliklinika s r o 70200 Ostrava Czech Republic

Department of Epidemiology and Public Health Faculty of Medicine University of Ostrava 70030 Ostrava Czech Republic

Department of Hemato oncology University Hospital of Ostrava 70800 Ostrava Czech Republic

Department of Immunology Faculty of Medicine and Dentistry Palacky University Olomouc 77515 Olomouc Czech Republic

Department of Immunology Public Health Institute in Ostrava 70200 Ostrava Czech Republic

Department of Intensive Medicine Emergency Medicine and Forensic Studies University of Ostrava 71000 Ostrava Czech Republic

Department of Lung Disease and Tuberculosis University Hospital Ostrava 70800 Ostrava Czech Republic

Department of Medical Microbiology Prague and Kladno Public Health Institute in Ústí nad Labem 18600 Prague Czech Republic

Department of Microbiology Faculty of Medicine and Dentistry Palacky University Olomouc 77515 Olomouc Czech Republic

Department of Pneumology and Phthisiology Ostrava City Hospital 72880 Ostrava Czech Republic

Division of Infectious Diseases and Geographic Medicine Stanford University School of Medicine Stanford CA 95128 USA

Institute of Laboratory Medicine Faculty of Medicine University of Ostrava 70300 Ostrava Czech Republic

Institute of Microbiology of the Czech Academy of Sciences 14220 Prague Czech Republic

Institute of Physiology and Pathophysiology Faculty of Medicine University of Ostrava 71000 Ostrava Czech Republic

Lung Department Krnov Combined Medical Facility 79401 Krnov Czech Republic

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