4.2 Article

Preactivation with IL-12, IL-15, and IL-18 Induces CD25 and a Functional High-Affinity IL-2 Receptor on Human Cytokine-Induced Memory-like Natural Killer Cells

期刊

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
卷 20, 期 4, 页码 463-473

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2014.01.006

关键词

NK cell; Adoptive immunotherapy; Cytokine; IL-2; IL-2 receptor

资金

  1. American Society of Hematology (ASH) Trainee Award
  2. NIH [T32 HL708836, K08HL093299]
  3. V Foundation for Cancer Research
  4. ASH Foundation

向作者/读者索取更多资源

Natural killer (NK) cells are effector lymphocytes that are under clinical investigation for the adoptive immunotherapy of hematologic malignancies, especially acute myeloid leukemia. Recent work in mice has identified innate memory-like properties of NK cells. Human NK cells also exhibit memory-like properties, and cytokine-induced memory-like (CIML) NK cells are generated via brief preactivation with IL-12, IL-15, and IL-18, which later exhibit enhanced functionality upon restimulation. However, the optimal cytokine receptors and signals for maintenance of enhanced function and homeostasis after preactivation remain unclear. Here, we show that IL-12, IL-15, and IL-18 preactivation induces a rapid and prolonged expression of CD25, resulting in a functional high-affinity IL-2 receptor (IL-2R alpha beta gamma) that confers responsiveness to picomolar concentrations of IL-2. The expression of CD25 correlated with STAT5 phosphorylation in response to picomolar concentrations of IL-2, indicating the presence of a signal-competent IL-2R alpha beta gamma. Furthermore, picomolar concentrations of IL-2 acted synergistically with IL-12 to costimulate IFN-gamma production by preactivated NK cells, an effect that was CD25 dependent Picomolar concentrations of IL-2 also enhanced NK cell proliferation and cytotoxicity via the IL-2R alpha beta gamma. Further, after adoptive transfer into immunodeficient NOD-SCID-gamma c(-/-) mice, human cytokine preactivated NK cells expand preferentially in response to exogenous IL-2. Collectively, these data demonstrate that human CIML NK cells respond to IL-2 via IL-2R alpha beta gamma(43y with enhanced survival and functionality, and they provide additional rationale for immunotherapeutic strategies that include brief cytokine preactivation before adoptive NK cell transfer, followed by low-dose IL-2 therapy. (c) 2014 American Society for Blood and Marrow Transplantation.

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