Direct Measurement of CD34 + Blood Stem Cell Absolute Counts by Flow Cytometry
Open Access
- 1 July 1998
- journal article
- research article
- Published by Oxford University Press (OUP) in The International Journal of Cell Cloning
- Vol. 16 (4) , 294-300
- https://doi.org/10.1002/stem.160294
Abstract
For the collection of adequate numbers of peripheral blood stem cells (PBSC) for PBSC transplantation, an accurate quantification of circulating CD34+ stem cells is required for deciding the optimal time of the collection. To enumerate peripheral blood (PB) CD34+ stem cells, the percentage of CD34+ cells in the gated PB mononuclear cells should be multiplied by the percentage of the gated mononuclear cells among white blood cells (WBC) and by the total WBC count. Accordingly, a minor difference in the measured percentage of the CD34+ cells can lead to a major difference in the PB CD34+ cell concentration. In the present study, we measured the concentration of PB CD34+ stem cells with a flow cytometer designed to provide direct absolute counts of cell subsets from a single instrument. Whole blood was stained with a phycoerythrin-conjugated anti-CD34 monoclonal antibody, and, after the lysis of red blood cells, CD34+ cells were counted in a fraction of the lymphocyte and monocyte gate. The accuracy of our method was demonstrated in an experiment in which various dilutions of known numbers of CD34+ leukemic cells were mixed with normal blood; the predicted value of the CD34+ cell count was observed. The concentration of CD34+ cells in leukapheresis products was measured both by our direct assay and an indirect assay that calculates the number from the percentage of CD34+ cells in mononuclear cells, and our assay was shown to produce less variation. Further, our assay showed a significant correlation between the concentration of mobilized CD34+ cells in the PB and the number of harvested CD34+ cells in leukapheresis. These findings indicate that the monitoring of the concentration of PB CD34+ cells by the present method can be used to predict the number of stem cells collected in leukapheresis. This procedure is easy to perform and can be applied to daily monitoring to decide the appropriate timing for harvest of mobilized stem cells.Keywords
This publication has 17 references indexed in Scilit:
- CD34 counts to predict the adequate collection of peripheral blood progenitor cellsBone Marrow Transplantation, 1997
- The Influence of Flow Cytometric Gating Strategy on the Standardization of CD34+ Cell Quantitation: An Australian Multicenter StudyJournal of Hematotherapy, 1996
- Improved Priming for Mobilization of and Optimal Timing for Harvest of Peripheral Blood Stem CellsJournal of Hematotherapy, 1996
- The ISHAGE Guidelines for CD34+ Cell Determination by Flow CytometryJournal of Hematotherapy, 1996
- North American Multicenter Study on Flow Cytometric Enumeration of CD34+ Hematopoietic Stem CellsJournal of Hematotherapy, 1996
- Standardization of absolute CD4+ lymphocyte counts across laboratories: An evaluation of the ortho CytoronAbsolute flow cytometry system on normal donorsCytometry, 1995
- Peripheral blood stem cells (PBSCs) collected after recombinant granulocyte colony stimulating factor (rhG‐CSF): an analysis of factors correlating with the tempo of engraftment after transplantationBritish Journal of Haematology, 1994
- Peripheral Blood Progenitor Cell Transplantation Estimated by Three-Colour (CD34, HLA-DR, CD33) Flow CytometryActa Haematologica, 1994
- Precursors of colony-forming cells in humans can be distinguished from colony-forming cells by expression of the CD33 and CD34 antigens and light scatter properties.The Journal of Experimental Medicine, 1989
- Antigen CD34+ marrow cells engraft lethally irradiated baboons.Journal of Clinical Investigation, 1988