Loeffler Juergen, Haddad Ziad, Bonin Michael, Romeike Nele, Mezger Markus, Schumacher Ulrike, Kapp Markus, Gebhardt Florian, Grigoleit Goetz-Ulrich, Stevanović Stefan, Einsele Hermann, Hebart Holger
Department of Hematology and Oncology, Medizinische Klinik II, University of Würzburg, Würzburg, Germany.
Department of Hematology and Oncology, Tübingen University Hospital, Tübingen, Germany.
J Med Microbiol. 2009 Jan;58(Pt 1):49-58. doi: 10.1099/jmm.0.003293-0.
Monocytes play a major role in the cellular defence against Aspergillus fumigatus in immunocompromised patients. To obtain a better understanding of the mechanisms involved in this interaction, phagocytosis and gene expression profiling of human monocytes was carried out after incubation with A. fumigatus resting, swollen and germinating conidia and hyphae (for 3, 6 and 9 h). The majority of monocytes phagocytosed up to three conidia during the first 3 h of incubation. Microarray analysis showed an increased expression level of immune-relevant genes, which was dependent on the germination state of the fungus and the incubation period. Among these genes, those encoding interleukin-8, macrophage inflammatory protein 3-alpha (CCL20) and monocyte chemotactic protein-1 (CCL2) were found to be potential key regulators involved in the A. fumigatus-induced immune response. In addition, A. fumigatus was found to be an inducer of the genes encoding urokinase type plasminogen activator (uPA), urokinase type plasminogen activator receptor (uPAR),plasminogen activator inhibitor (PAI), pentraxin-3 (PTX3) and intercellular adhesion molecule-1 (ICAM-1), which, in combination, may contribute to thrombosis and local lung tissue injury.
