Title of article
Efficient monocyte-derived dendritic cell generation in patients with acute myeloid leukemia after chemotherapy treatment: Application to active immunotherapy
Author/Authors
Pierre-Joseph Royer، نويسنده , , Gwenola Bougras، نويسنده , , Frederic Ebstein، نويسنده , , Lucie Leveque، نويسنده , , Severine Tanguy-Royer، نويسنده , , Thomas Simon، نويسنده , , Nadine Juge-Morineau، نويسنده , , Patrice Chevallier، نويسنده , , Jean-Luc Harousseau، نويسنده , , Marc Gregoire، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2008
Pages
11
From page
329
To page
339
Abstract
Objective
While complete remission in acute myeloid leukemia (AML) can be achieved after chemotherapy (CT), relapses occur for the majority of patients, underlying the need to eliminate residual disease. Based on dendritic cell (DC) vaccination, the triggering of an immune response against residual leukemia cells after CT could maintain patients in remission. The aim of our study was to assess, for vaccine preparation, generation of monocyte-derived DCs in AML patients after CT.
Materials and Methods
We evaluated efficiency of the production, yields, maturation, and functional properties of DCs from 22 AML patients at different CT stages compared to those from 15 healthy donors.
Results
We demonstrated that monocyte-derived DC production is successful later than 3 weeks after the last CT cycle, whatever the CT was. Immature DCs demonstrated functional phagocytic activity. Mature DCs displayed migratory, T-cell stimulatory and Th1-activation capacities. Our results also suggest a favorable period from 20 to 60 days after CT for potent monocyte-derived DC production and immune activation.
Conclusion
In defining patient-sampling conditions, this preclinical study has direct implications for AML DC-based immunotherapy.
Journal title
Experimental Hematology
Serial Year
2008
Journal title
Experimental Hematology
Record number
514749
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