Ij. Webb et al., Predictors of high yield and purity of CD34(+) cell-selected PBPC, collected from patients with multiple myeloma, CYTOTHERAPY, 1(3), 1999, pp. 175-182
Citations number
36
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
Background Wide ranges in cell recovery and purity may be observed followin
g CD34(+) cell selection of mobilized HPC components. Characteristics of th
e mobilized HPC, associated with isolation of a high CD34(+) cell yield and
purity following cell selection, have yet to be defined.
Methods Cell numbers and purities were determined before and after 56 CD34(
+) cell-selection procedures, performed using the CellPro Ceprate SC system
from April 1997 to February 1998. HPC were collected from 28 patients with
multiple myeloma, following cyclophosphamide (60 mg/kg) and G-CSF (10 mu g
/kg) mobilization.
Results. A median of 47.9% (range 1.5-109.6%) CD34(+) cells were recovered
ill the enriched (ENR) fraction. A linear correlation existed between total
CD34(+) cells in the ENR fraction and total CD34(+) cells in the START fra
ction (R2 = 0.93); there was a log-arithmic correlation between CD34 ENR fr
action purity and START fraction purity (R2 = 0.73). A START CD34(+) cell p
urity > 0.42% improved purity in the ENR fraction. A median of one (range o
ne to nine) procedure was required to isolate 2 x 10(6) CD34(+) cells/kg. T
hree patients pretreated with alkylating agents failed to mobilize adequate
numbers of HPC.
Discussion Isolation of highly purified CD34(+) cell-selected components us
ing the Ceprate SC system is dependent on the CD34(+) purity of the leukaph
eresis component collected. Mobilization regimens should be used to maximiz
e CD34(+) cell purity in stem cell autografts if CD34(+) cell selection is
to be performed. Similar strategies should be used to evaluate other cell-s
election devices as they become available.