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DOI 10.1093/infdis/jiaa035

Медицинская библиотека · The Journal of infectious diseases · 2020

Candida Species-Dependent Release of IL-12 by Dendritic Cells Induces Different Levels of NK Cell Stimulation.

Marolda Alessandra, Hünniger Kerstin, Böttcher Sarah, Vivas Wolfgang, Löffler Jürgen, Figge Marc Thilo, Kurzai Oliver

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

Candida albicans and Candida glabrata are the 2 most prevalent Candida species causing bloodstream infections. Patterns of innate immune activation triggered by the 2 fungi differ considerably.

METHODS

To analyze human natural killer (NK) cell activation by both species, we performed ex vivo whole-blood infection assays and confrontation assays with primary human NK cells.

RESULTS

C. albicans was a stronger activator for isolated human NK cells than C. glabrata. In contrast, activation of blood NK cells, characterized by an upregulated surface exposure of early activation antigen CD69 and death receptor ligand TRAIL, as well as interferon-γ (IFN-γ) secretion, was more pronounced during C. glabrata infection. NK cell activation in blood is mediated by humoral mediators released by other immune cells and does not depend on direct activation by fungal cells. Cross-talk between Candida-confronted monocyte-derived dendritic cells (moDC) and NK cells resulted in the same NK activation phenotype as NK cells in human blood. Blocking experiments and cytokine substitution identified interleukin-12 as a critical mediator in regulation of primary NK cells by moDC.

CONCLUSIONS

Activation of human NK cells in response to Candida in human blood mainly occurs indirectly by mediators released from monocytic cells.

Для цитирования: Marolda Alessandra, Hünniger Kerstin, Böttcher Sarah, Vivas Wolfgang, Löffler Jürgen, Figge Marc Thilo, Kurzai Oliver. Candida Species-Dependent Release of IL-12 by Dendritic Cells Induces Different Levels of NK Cell Stimulation.. The Journal of infectious diseases. 2020. DOI: 10.1093/infdis/jiaa035.

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