Induction of myeloma-specific cytotoxic T lymphocytes responses by natural killer cells stimulated-dendritic cells in patients with multiple myeloma

Leuk Res. 2011 Sep;35(9):1241-7. doi: 10.1016/j.leukres.2011.03.032. Epub 2011 May 25.

Abstract

The interaction between dendritic cells (DCs) and natural killer (NK) cells plays a key role in inducing DC maturation for subsequent T-cell priming. We investigated to generate potent DCs by stimulated with NK cells to induce myeloma-specific cytotoxic T lymphocytes (CTLs). NK cells-stimulated-DCs exhibited high expression of costimulatory molecules and high production of IL-12p70. These DCs induce high potency of Th1 polarization and exhibit a high ability to generate myeloma-specific CTLs responses. These results suggest that functionally potent DCs can be generated by stimulation with NK cells and may provide an effective source of DC-based immunotherapy in multiple myeloma.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Polarity / drug effects
  • Cell Polarity / immunology
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Cytotoxicity, Immunologic / drug effects
  • Cytotoxicity, Immunologic / physiology
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology*
  • Dendritic Cells / pathology
  • HL-60 Cells
  • Humans
  • Interferon Type I / pharmacology
  • K562 Cells
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / pathology
  • Killer Cells, Natural / physiology*
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / immunology
  • Lymphocyte Activation / physiology*
  • Multiple Myeloma / immunology*
  • Multiple Myeloma / pathology
  • Polydeoxyribonucleotides / pharmacology
  • Recombinant Proteins
  • T-Cell Antigen Receptor Specificity / drug effects
  • T-Cell Antigen Receptor Specificity / immunology
  • T-Lymphocytes, Cytotoxic / drug effects
  • T-Lymphocytes, Cytotoxic / immunology*
  • T-Lymphocytes, Cytotoxic / pathology

Substances

  • Interferon Type I
  • Polydeoxyribonucleotides
  • Recombinant Proteins
  • poly d(I-C)