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      Comparison of monocyte enrichment by immuno-magnetic depletion or adherence for the clinical-scale generation of DC.

      Cytotherapy
      Antigens, CD19, immunology, Antigens, CD2, B-Lymphocytes, cytology, Cell Adhesion, Cell Culture Techniques, instrumentation, methods, Cell Division, Cell Separation, Cell Survival, Dendritic Cells, Dextrans, metabolism, Flow Cytometry, Humans, Immunomagnetic Separation, Immunophenotyping, Monocytes, Pinocytosis, T-Lymphocytes

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          Abstract

          DC generated from monocytes have been used for vaccines. We have developed a monocyte enrichment procedure by depleting T and B cells with anti-CD2 and anti-CD19 Abs using the automated Isolex 300i magnetic cell selector for clinical-scale DC generation in gas permeable SteriCell culture bags. We have also compared DC function, yield and purity of DC generated from adherent monocytes using culture bags in a closed system, with DC generated in conventional tissue culture flasks. Monocytes were enriched from normal donor apheresis products using CD2/19 depletion with experimental software on the Isolex 300i (ISO), adherence (AD) to SteriCell bags and to T175 flasks and then cultured for 7 days in serum-free X-VIVO 15 media with GM-CSF and IL-4. Phenotype and dextran uptake were analyzed by flow cytometry and allogeneic MLR was also evaluated. ISO-DC and AD-DC from SteriCell bags showed similar viability. Higher purity of ISO-DC than AD-DC was measured by forward- and side-scatter flow cytometry. Similar expression of CD1a, CD80, CD86 and CD83 were observed in both ISO-DC and AD-DC. Similar dextran uptake and allo MLR were also observed. These data indicated that functional DC were generated in gas permeable SteriCell culture bags from both ISO- and AD-monocytes in a closed system.

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