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Strunk, D; Rohde, E; Lanzer, G; Linkesch, W.
Phenotypic characterization and preclinical production of human lineage-negative cells for regenerative stem cell therapy.
TRANSFUSION. 2005; 45: 315-326. Doi: 10.1111/j.1537-2995.2005.04056.x
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Führende Autor*innen der Med Uni Graz
Strunk Dirk
Co-Autor*innen der Med Uni Graz
Lanzer Gerhard
Linkesch Werner
Rohde Eva
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Abstract:
BACKGROUND: Regenerative stem cell therapy (SCT) is currently being tested in clinical trials. The ideal type and source of cells have not yet been defined. Lineage (Lin) depletion is an experimental procedure capable of enriching all recently recognized SC types with regenerative potency. This study was performed to define a practicable monoclonal antibody (MoAb) cocktail for Lin depletion and to test whether clinical-scale Lin depletion is possible. STUDY DESIGN AND METHODS: MoAbs (CD2/14/15/19/41/56/glycophorin A) were selected to mark seven mature hematopoietic lineages. Lin7-negative (Lin7NEG) cells were analyzed in peripheral blood (PB, n = 9), mobilized PB (MPB, n = 5), umbilical cord blood (UCB, n = 5), and marrow aspirates (BM, n = 4) by flow cytometry. Preclinical Lin depletion was tested with leukapheresis products from PB following good manufacturing practice (GMP) principles. RESULTS: Lin7NEG cells comprised 0.23 +/- 0.04, 0.27 +/- 0.03, 0.53 +/- 0.07, and 0.49 +/- 0.03 percent of PB, MPB, UCB, and BM, respectively. Basophils, CD34+, and dendritic cells constituted the major Lin7NEG subpopulations (84 +/- 2, 90 +/- 3, 40 +/- 3, and 80 +/- 3% in PB, MPB, UCB, and BM, respectively). Minor populations included CD7- and CD45- cells. Preclinical CD2/14/15/19/56 (Lin5) depletion after automated red blood cell and platelet reduction resulted in up to a 16.7-fold enrichment of CD34+ and CD34-/Lin5NEG cells. CONCLUSIONS: A seven-MoAb cocktail is sufficient to label more than 99 percent of nucleated cells in PB, MPB, UCB, and BM. Preclinical Lin depletion can be performed under GMP conditions from PB apheresis procedures.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Antibodies, Monoclonal - immunology
Biological Markers - immunology
Cell Lineage - immunology
Cell Separation - methods
Female - methods
Flow Cytometry - methods
Fluorescent Antibody Technique - methods
Hematopoietic Stem Cell Transplantation - methods
Hematopoietic Stem Cells - cytology
Humans - cytology
Immunophenotyping - cytology
Leukapheresis - methods
Male - methods
Membrane Proteins - immunology
Middle Aged - immunology

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