M. Elias and J. van Zanten contributed equally to this manuscript.
Closed system generation of dendritic cells from a single blood volume for clinical application in immunotherapy†
Article first published online: 12 MAY 2005
Copyright © 2005 Wiley-Liss, Inc.
Journal of Clinical Apheresis
Volume 20, Issue 4, pages 197–207, December 2005
How to Cite
Elias, M., van Zanten, J., Hospers, G.A.P., Setroikromo, A., de Jong, M.A., de Leij, L.F.M.H. and Mulder, N.H. (2005), Closed system generation of dendritic cells from a single blood volume for clinical application in immunotherapy. J. Clin. Apheresis, 20: 197–207. doi: 10.1002/jca.20054
- Issue published online: 8 DEC 2005
- Article first published online: 12 MAY 2005
- Manuscript Accepted: 4 FEB 2005
- Manuscript Received: 23 NOV 2004
Dendritic cells (DC) used for clinical trials should be processed on a large scale conforming to current good manufacturing practice (cGMP) guidelines. The aim of this study was to develop a protocol for clinical grade generation of immature DC in a closed-system. Aphereses were performed with the Cobe Spectra™ continuous flow cell separator and material was derived from one volume of blood processed. Optimisation of a 3-phase collection autoPBSC technique significantly improved the quality of the initial mononuclear cell (MNC) product. Monocytes were then enriched from MNC by immunomagnetic depletion of CD19+ B cells and CD2+ T cells and partial depletion of NK cells using the Isolex 300I Magnetic cell selector. The quality of the initial mononuclear cell product was found to determine the outcome of monocyte enrichment. Enriched monocytes were cultured in Opticyte gas-permeable containers using CellGro serum-free medium supplemented with GM-CSF and IL-4 to generate immature DC. A seeding concentration of 1 × 106 was found optimal in terms of DC phenotype expression, monocyte percentage in culture, and cell viability. The differentiation pattern favours day 7 for harvest of immature DC. DC recovery, viability, as well as phenotype expression after cryopreservation of immature DC was considered in this study. DC were induced to maturation and evaluated in FACS analysis for phenotype expression and proliferation assays. Mature DC were able to generate an allogeneic T-cell response as well as an anti-CMV response as detected by proliferation assays. These data indicate that the described large-scale GMP-compatible system results in the generation of stable DC derived from one volume of blood processed, which are qualitatively and quantitatively sufficient for clinical application in immunotherapeutic protocols. J. Clin. Apheresis © 2005 Wiley-Liss, Inc.