IL-12/15/18-preactivated NK cells suppress GvHD in a mouse model of mismatched hematopoietic cell transplantation

Eur J Immunol. 2015 Jun;45(6):1727-35. doi: 10.1002/eji.201445200. Epub 2015 Apr 17.

Abstract

Mismatched hematopoietic cell transplants for treating leukemia are complicated by graft versus host disease (GvHD). Here, we show that adoptively transferred IL-12/15/18-preactivated NK cells suppress GvHD in a mouse model of fully mismatched hematopoietic cell transplantation. These IL-12/15/18-preactivated NK cells maintained Eomesodermin (Eomes) and T-bet expression upon transfer and, while there was no evidence of direct killing of donor T cells or host DCs by the IL-12/15/18-preactivated NK cells, proliferation of donor T cells was inhibited. Strikingly, the graft versus leukemia effect mediated by donor T cells was retained, resulting in improved overall survival of mice that received lymphoma cells, donor allogeneic T cells, and IL-12/15/18-preactivated NK cells. These results suggest that IL-12/15/18-preactivated NK cells may be useful in improving immunotherapy of mismatched hematopoietic cell transplantation. Compared with previously proposed protocols, our findings suggest that in vitro NK-cell preactivation with this cytokine cocktail offers the significant advantage that cytokines do not need to be administered systemically to sustain NK-cell activity, thus avoiding toxicity.

Keywords: Cytokine-induced NK cells; GvHD; HSCT; Lymphoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytokines / pharmacology
  • Disease Models, Animal
  • Female
  • Gene Expression
  • Graft vs Host Disease / etiology*
  • Graft vs Host Disease / therapy
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Immunotherapy, Adoptive*
  • Interferon-gamma / biosynthesis
  • Interleukin-12 / pharmacology
  • Interleukin-15 / pharmacology
  • Interleukin-18 / pharmacology
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / immunology*
  • Mice
  • Phenotype
  • T-Box Domain Proteins / genetics
  • T-Box Domain Proteins / metabolism
  • Transplantation Chimera
  • Transplantation, Homologous

Substances

  • Cytokines
  • Eomes protein, mouse
  • Interleukin-15
  • Interleukin-18
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • Interleukin-12
  • Interferon-gamma