Primitive quiescent CD34+ cells in chronic myeloid leukemia are targeted by in vitro expanded natural killer cells, which are functionally enhanced by bortezomib

Blood. 2009 Jan 22;113(4):875-82. doi: 10.1182/blood-2008-05-158253. Epub 2008 Oct 15.

Abstract

Primitive quiescent CD34(+) chronic myeloid leukemia (CML) cells are more biologically resistant to tyrosine kinase inhibitors than their cycling counterparts; however, graft-versus-leukemia (GVL) effects after allogeneic stem cell transplantation (SCT) probably eliminate even these quiescent cells in long-term surviving CML transplant recipients. We studied the progeny of CD34(+) cells from CML patients before SCT, which were cultured 4 days in serum-free media with hematopoietic growth factors. BCR-ABL expression was similar in both cycling and quiescent noncycling CD34(+) populations. Quiescent CD34(+) cells from CML patients were less susceptible than their cycling CD34(+) and CD34(-) counterparts to lysis by natural killer (NK) cells from their HLA-identical sibling donors. Compared with cycling populations, quiescent CD34(+) CML cells had higher surface expression of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) receptors DR4 and DR5. Bortezomib up-regulated TRAIL receptor expression on quiescent CD34(+) CML cells, and further enhanced their susceptibility to cytotoxicity by in vitro expanded donor NK cells. These results suggest that donor-derived NK cell-mediated GVL effects may be improved by sensitizing residual quiescent CML cells to NK-cell cytotoxicity after SCT. Such treatment, as an adjunct to donor lymphocyte infusions and pharmacologic therapy, may reduce the risk of relapse in CML patients who require treatment by SCT.

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD34 / metabolism*
  • Boronic Acids / pharmacology*
  • Bortezomib
  • Cell Separation
  • Cells, Cultured
  • Female
  • Gene Expression Regulation, Neoplastic / genetics
  • Genetic Predisposition to Disease / genetics
  • Genotype
  • Humans
  • Killer Cells, Natural / cytology*
  • Killer Cells, Natural / drug effects*
  • Killer Cells, Natural / immunology
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / immunology
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / metabolism*
  • Male
  • Middle Aged
  • Monomeric GTP-Binding Proteins / genetics
  • Monomeric GTP-Binding Proteins / metabolism
  • Pyrazines / pharmacology*
  • Receptors, Death Domain / metabolism
  • Up-Regulation / drug effects

Substances

  • Antigens, CD34
  • Boronic Acids
  • Pyrazines
  • Receptors, Death Domain
  • Bortezomib
  • GEM protein, human
  • Monomeric GTP-Binding Proteins