HLA-DR+ NK cells are mostly characterized by less mature phenotype and high functional activity

Immunol Cell Biol. 2018 Feb;96(2):212-228. doi: 10.1111/imcb.1032. Epub 2017 Dec 19.

Abstract

NK cells change their phenotype and functional characteristics during activation. In this work, we searched for a relationship of HLA-DR expression with differentiation stages and functional activity of NK cells ex vivo and stimulated in vitro with IL-2 challenged with gene modified feeder K562 cells expressing membrane-bound IL-21 (K562-mbIL21). This stimulation technique has been described for NK cell expansion in clinical use. We have observed that HLA-DR expression in freshly isolated circulating NK cells was mostly associated with less differentiated CD56bright CD57- cells, although in some individuals it could also be found in terminally differentiated CD57+ cells. Ex vivo HLA-DR+ NK cells possessed better capacity to produce IFN-γ in response to cytokine stimulation compared to their HLA-DR- counterparts. In vitro activation with IL-2 and K562-mbIL21 induces an increase in HLA-DR-positive NK cell proportion, again mostly among CD56bright CD57- NK cells. This happened in particular due to appearance of HLA-DR+ expression de novo in HLA-DR-negative cells. Acquired in vitro HLA-DR expression was associated with NK cell proliferation activity, more intense cytokine-induced IFN-γ production, increased degranulation toward feeder cells, and higher expression of CD86 and NKG2D. Thus, stimulation with IL-2/K562-mbIL21 causes a significant phenotype and functional shift during NK cell activation and expansion.

Keywords: HLA-DR; Human NK cells; IL-2; IL-21; NK cell activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / metabolism
  • Cell Death
  • Cell Differentiation
  • Cell Proliferation
  • Cell Separation
  • Cytotoxicity, Immunologic
  • HLA-DR Antigens / metabolism*
  • Humans
  • Interferon-gamma / metabolism
  • Interleukin-2 / metabolism
  • K562 Cells
  • Killer Cells, Natural / cytology*
  • Killer Cells, Natural / immunology*
  • Phenotype

Substances

  • Biomarkers
  • HLA-DR Antigens
  • Interleukin-2
  • Interferon-gamma