Journal of Hematotherapy · 1995 · 64 citations · 18 references
Life SciencesCell BiologyHematologyCell TherapyChemotherapyStem Cell BiologyCellular TherapyHematopoietic DevelopmentHematopoietic DifferentiationHematopoietic Stem Cell BiologyHematopoietic Stem Cell TransplantationHematopoietic Stem CellsBone Marrow - Derived CellsCd34 Positive SelectionEx Vivo Cell ExpansionEx Vivo Stem Cell ExpansionHematopoietic Stem Cell ExpansionMultipotent ProgenitorsSelection Of Hematopoietic ProgenitorsTransplantation For Hematologic Malignancies
A large volume culture system was developed for the ex vivo expansion of CD34 positive (+) hematopoietic progenitors, using cell donated by 15 patients receiving high-dose chemotherapy with autologous hematopoietic progenitor cell support (AHPCS). Substantial expansion of myeloid (181-fold) and megakaryocyte (41-fold) progenitors cells was demonstrated, using the conditions that we determined to be optimal: CD34+ progenitors cultured unperturbed for 7 (marrow) or 10 (blood) days in Teflon-coated bags with X-Vivo-10 medium containing 10% autologous plasma, 100 ng/ml, respectively, of recombinant stem cell factor (SCF), interleukin 3 (IL-3), interleukin 6 (IL-6), and granulocyte colony-stimulating factor (G-CSF). The studies demonstrated that (a) CD34 selection was necessary to obtain large, clinically relevant numbers of hematopoietic progenitors, (b) the addition of G-CSF to the baseline regimen of SCF/IL-3/IL-6 significantly enhanced the expansion of myeloid progenitors, (c) the addition of IL-1 to SCF/IL-3/IL-6 did not significantly enhance myeloid progenitor cell expansion, (d) CD34+ G-CSF-mobilized peripheral blood progenitor cells (PBPC) produced higher numbers of myeloid progenitors in culture than CD34+ marrow cells, and (e) long-term tissue culture (LTC) assays demonstrate the preservation of long-term initiating cells in ex vivo culture. The short-term and long-term reconstituting capability of CD34+ PBPC cultured in this system remains to be determined and will be evaluated in a clinical trial where they will be used as the sole source of AHPCS following high-dose therapy.
18
Rosemary Ford, Seth Eisenberg · Nursing Clinics of North America · 1990 · 2.7K citations
H.J. Sutherland, Peter M. Lansdorp, D Henkelman et al. · Proceedings of the National Academy of Sciences · 1990 · 678 citations
Elizabeth J. Shpall, Roy B. Jones, Scott I. Bearman et al. · Journal of Clinical Oncology · 1994 · 393 citations
Medicine, Hematology, Oncology +17