Immunotherapy using autologous monocyte-derived dendritic cells pulsed with leukemic cell lysates for acute myeloid leukemia relapse after autologous peripheral blood stem cell transplantation

J Clin Apher. 2004;19(2):66-70. doi: 10.1002/jca.10080.

Abstract

Although a second stem cell transplantation (SCT) can be used as salvage therapy in patients with relapsing leukemia after SCT, most of these patients have a poor outcome. We tried clinical vaccination using monocyte-derived dendritic cells (DCs) pulsed with leukemic lysates to treat relapsing acute myeloid leukemia (AML) after autologous SCT. To generate DCs, CD14+ cells isolated from peripheral blood stem cell products were cultured in AIM-V in the presence of GM-CSF and IL-4. Adding TNF-alpha on day 6 induced maturation of the DCs, which were harvested on day 8 or 9. The DCs were incubated with tumor lysate and KLH for 2 hr at 37 degrees C. After certifying the absence of microorganisms and endotoxins, the patients received four DC vaccinations at two- to three-week intervals. Two patients received four DC vaccinations with means of 7.8 x 10(6) and 9 x 10(6) DCs at two- to three-week intervals. The DC vaccinations were well tolerated with no apparent side effects. After the vaccinations, the patients showed immunological responses with positive delayed-type hypersensitivity skin reaction and increasing autologous T cells stimulatory capacity to the DCs; however, the BM blast percentage of the patients did not improve. The results suggest that DCs are a feasible cellular therapy for relapsing AML after autologous SCT.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • CD3 Complex / biosynthesis
  • Cell Separation
  • Dendritic Cells / cytology*
  • Female
  • Flow Cytometry
  • Humans
  • Immunotherapy / methods*
  • Interleukin-4 / metabolism
  • Leukemia, Myeloid, Acute / pathology*
  • Leukemia, Myeloid, Acute / therapy*
  • Lipopolysaccharide Receptors / biosynthesis
  • Male
  • Monocytes / metabolism*
  • Peripheral Blood Stem Cell Transplantation / methods*
  • Phenotype
  • Recurrence
  • Stem Cell Transplantation
  • Temperature
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • CD3 Complex
  • Lipopolysaccharide Receptors
  • Tumor Necrosis Factor-alpha
  • Interleukin-4