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    Plasmacytoid dendritic cell depletion modifies FoxP3+ T cell homeostasis and the clinical course of bacterial pneumonia in mice (2019)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Lippitsch, Anne
    Baal, Nelli
    Chukovetskyi, Yuri
    Cunningham, Sarah
    Michel, Gabriela
    Dietert, Kristina (WE 12)
    Gurtner, Corinne
    Gruber, Achim D. (WE 12)
    Bein, Gregor
    Hackstein, Holger
    Quelle
    Journal of leukocyte biology : JLB
    Bandzählung: 106
    Heftzählung: 4
    Seiten: 977 – 985
    ISSN: 1938-3673
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://jlb.onlinelibrary.wiley.com/doi/full/10.1002/JLB.3AB0119-014RR
    DOI: 10.1002/JLB.3AB0119-014RR
    Pubmed: 31265764
    Kontakt
    Institut für Tierpathologie

    Robert-von-Ostertag-Str. 15
    14163 Berlin
    +49 30 838 62450
    pathologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    Plasmacytoid dendritic cells (pDC) are critical to antiviral defense because of their high production of type I IFNs; less is known regarding their functions in bacterial infection. Moreover, pDC are involved in immunomodulation. A stable pool of regulatory T cells (Treg) is crucial for maintaining immune homeostasis. However, interactions between pDC and Treg regarding the regulation of Treg homeostasis are understudied. By using BDCA2-DTR mice as a systemic pDC depletion model, we identified increased steady-state numbers of FoxP3+ T cells with an effector Treg-like phenotype in lungs, liver, and spleen tissues. During sublethal, pulmonary Klebsiella pneumoniae infection, pDC deficiency also elevated respiratory FoxP3+ T cell numbers. Additionally, the improvement in acute pneumonia survival until day 5 post infection was accompanied by impaired proinflammatory cytokine production. In contrast, pDC-depleted mice exhibited a delayed clinical recovery during the post-acute phase. Therefore, we assume that pDC act as immunomodulators supporting the rapid onset of immune response in a proinflammatory manner and regulate inflammation or tissue regeneration in the post-acute phase. In summary, pDC assist in FoxP3+ T cell homeostasis and the regulation of Klebsiella-pneumonia progression.