Increased blood volume and CD34(+)CD38(-) progenitor cell recovery using anovel umbilical cord blood collection system

Citation
O. Belvedere et al., Increased blood volume and CD34(+)CD38(-) progenitor cell recovery using anovel umbilical cord blood collection system, STEM CELLS, 18(4), 2000, pp. 245-251
Citations number
26
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
STEM CELLS
ISSN journal
10665099 → ACNP
Volume
18
Issue
4
Year of publication
2000
Pages
245 - 251
Database
ISI
SICI code
1066-5099(2000)18:4<245:IBVACP>2.0.ZU;2-D
Abstract
A major problem with the use of umbilical cord/placental blood (UCB) is the limited blood volume that can be collected from a single donor. In this st udy, me evaluated a novel system for the collection of UCB and analyzed the kinetics of output of hematopoietic stem cells in the collected blood. Sequential UCB fractions were collected from 48 placentas by gravity follow ing common procedures. When UCB nom was ended, collection was continued usi ng the device. Nucleated cell (NC) density in each fraction was evaluated a nd the expression of CD34, CD38 and other hematopoietic markers was assesse d by flow cytometry. The total collected volume was 60.9 +/- 26.2 ml (mean +/- SD, range 17-141. 5). The device yield (volume collected using the device/total volume) was 2 6.5 +/- 15.1%. No significant difference was observed in NC count in sequen tial fractions. A significant increase in CD34(+) cell content in sequentia l fractions and a 2.07 +/- 1.18-fold increase in the percentage of CD34(+) cells in the last versus first fraction were observed. Furthermore, within the CD34(+) population, the percentage of CD38(-) pluripotent stem cells in the first fraction was 3.24 +/- 1.39, while in the last fraction it raised to 34.43 +/- 22.62. Thus, at the end of a collection performed following current procedures, fu rther blood rich in the most primitive progenitor cells can be recovered. T herefore, the optimization and standardization of collection procedures are required to obtain maximal recovery from each placenta and increase the pe rcentage of UCB units suitable for clinical use.