Detailseite
Projekt Druckansicht

Schwächung der innaten anti-bakteriellen Immunantwort in Chronischer Lymphatischer Leukämie

Fachliche Zuordnung Immunologie
Förderung Förderung von 2016 bis 2020
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 314635618
 
Erstellungsjahr 2020

Zusammenfassung der Projektergebnisse

Patients with chronic lymphocytic leukemia (CLL) suffer from frequent and severe bacterial infections. Although it is well known that neutrophils are critical innate immune cells facilitating the early defense, the underlying phenotypical and functional changes in neutrophils during CLL are elusive. Using the murine adoptive transfer model of CLL, we demonstrate aggravated bacterial burden in CLL- bearing mice upon a urinary tract infection of the urinary bladder with uropathogenic E.coli. Bioinformatic analyses of the neutrophil proteome revealed not only increased signatures of interferon-signaling, but also decreased protein expression associated with granule composition and neutrophil migration. Functional experiments validated these findings by showing reduced levels of myeloperoxidase and acidification of neutrophil granules after ex vivo phagocytosis of bacteria. Pathway enrichment analysis indicated decreased expression of molecules critical for neutrophil migration, and neutrophil migration in vivo into the infected urinary bladder was insufficient. The changed migration properties of neutrophils was also evident in the reduced expression of CD62L and CXCR4 in CLL-bearing mice and also treatment-naïve CLL patients showed a similar neutrophil phenotype (CD62Llow CXCR4low). In conclusion, this study describes through proteomic and functional analyzes a molecular signature of neutrophils, which is linked to a reduced and migratory ability, potentially leading to increased bacterial infections in CLL patients.

Projektbezogene Publikationen (Auswahl)

 
 

Zusatzinformationen

Textvergrößerung und Kontrastanpassung