Procedures for the expansion of CD14(+) precursors from acute myeloid leukemic cells to facilitate dendritic cell-based immunotherapy

Immunotherapy. 2013 Nov;5(11):1183-90. doi: 10.2217/imt.13.125.

Abstract

Aims: Vaccination with acute myeloid leukemia (AML)-derived dendritic cells (DCs) is a promising immunotherapeutic approach to prevent relapse of AML. However, in clinical practice AML-derived DC culture is unfeasible in 40% of cases. Here, we demonstrate that AML cells can be expanded in vitro prior to differentiation with cocktails of cytokines with known myeloid growth-promoting effects.

Results: Nine out of 13 initially CD14(-) samples gain de novo CD14 (>10%) expression (69% increment; p = 0.01) after in vitro expansion. These expanded CD14(+) leukemic cells displayed a high probability (six out of six initially CD14(-) samples tested) to differentiate into DCs upon culture with GM-CSF, TNF-α and IL-4.

Conclusion: Induction of CD14 on initially CD14(-) AML cells potentially increases the number of patients eligible for DC-based immunotherapy.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cytokines / immunology
  • Cytokines / pharmacology
  • Dendritic Cells* / immunology
  • Dendritic Cells* / transplantation
  • Female
  • Humans
  • Leukemia, Myeloid, Acute* / immunology
  • Leukemia, Myeloid, Acute* / therapy
  • Lipopolysaccharide Receptors / immunology*
  • Male
  • Vaccination*

Substances

  • Cytokines
  • Lipopolysaccharide Receptors