Published ahead of print on March 16, 2006, doi:10.1164/rccm.200508-1271OC
© 2006 American Thoracic Society doi: 10.1164/rccm.200508-1271OC
Chemokines Indicate Allergic Bronchopulmonary Aspergillosis in Patients with Cystic Fibrosis![]() ![]() Department of Pediatrics, University Hospital of Berne, Berne, Switzerland; Children's Hospital of the Ludwig-Maximilians-University of Munich, Munich; and Medical Center, Department of Pneumology, University Hospital, Freiburg, Germany Correspondence and requests for reprints should be addressed to Dominik Hartl, M.D., Research Center Kubus Dr., v. Haunersches Kinderspital Lindwurmstr., 2a D-80337 Munich, Germany. E-mail: dominic.hartl{at}med.uni-muenchen.de Rationale: Allergic bronchopulmonary aspergillosis (ABPA) is characterized by a Th2 immune response. Mouse models suggest a critical role for the Th2 chemokines thymus- and activation-regulated chemokine (TARC) and macrophage-derived chemokine (MDC) in ABPA. Objectives: To determine whether serum levels of TARC and MDC characterize ABPA in patients with cystic fibrosis (CF) and to examine longitudinally if levels of TARC and MDC indicate ABPA exacerbations in patients with CF.
Methods: Levels of TARC and MDC and levels of Th1 (IL-12 and IFN- Results: Patients with ABPA had significantly higher serum levels of TARC compared with the other patient groups. Cytokine levels did not differ among the patient groups. Longitudinally, levels of TARC indicated ABPA exacerbations in patients with CF more clearly than IgE levels. In patients with CF and ABPA, levels of TARC correlated positively with specific IgE to A. fumigatus and rAsp f4. Conclusions: Serum levels of TARC differentiate patients with CF or patients with asthma with ABPA from patients with CF colonized with or sensitized to A. fumigatus, atopic patients with CF, and atopic control subjects. Longitudinally, levels of TARC indicate ABPA exacerbations, suggesting TARC as a marker for identification and monitoring of ABPA in patients with CF.
Key Words: allergic bronchopulmonary aspergillosis chemokines cystic fibrosis TARC This article has been cited by other articles:
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