Counterflow centrifugation allows addition of appropriate numbers of T cells to allogeneic marrow and blood stem cell grafts to prevent severe GVHD without substantial loss of mature and immature progenitor cells
Fwmb. Preijers et al., Counterflow centrifugation allows addition of appropriate numbers of T cells to allogeneic marrow and blood stem cell grafts to prevent severe GVHD without substantial loss of mature and immature progenitor cells, BONE MAR TR, 23(10), 1999, pp. 1061-1070
Citations number
47
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
Using counterflow centrifugation elutriation (CCE) lymphocytes can be separ
ated from CD34(+) populations based on size. Immature progenitors tend to b
e smaller than mature cells suggesting that CCE introduces loss of stem cel
ls. We compared the separation of 12 PBSC with 16 BM transplants. Cells wer
e separated in 12 fractions (3000-2200 r.p.m.) and the rotor off (RO) fract
ion. Separation patterns of BM and PBSC were comparable. B cells were colle
cted in the high speed fractions followed by T and NK cells. In contrast, p
rogenitor cells were collected in lower speed fractions. By adding successi
vely T cell-depleted fractions to the RO fraction a BM transplant could be
composed containing 0.7 x 10(6) T cells/kg and 90%, 89% and 68% recovery of
CD34(+), CFU-GM and BFU-E. PBSC were separated in four CCE runs inducing h
igher numbers of T cells in the graft (4.4 x 10(6)/kg) and 54% CD34(+), 46%
CFU-GM and 37% BFU-E recovery. Time of engraftment was not delayed and no
graft failure was observed. The higher number of T cells was not associated
with higher incidence of GVHD. Acute GVHD greater than or equal to grade I
II occurred in 0 of 16 BM and two of 12 PBSC recipients; extensive chronic
GVHD was observed in four of 15 and three of nine recipients, respectively.
To study immature cells in the graft, CD34 subpopulations and cells with l
ong-term repopulating ability, determined using cobble-stone area formation
(CAFC assay), were evaluated in each fraction. The separation patterns in
BM and PBSC were comparable. Cells with mature and immature phenotype were
enriched in lower speed fractions (mean recovery of 74% CD34(+)/CD13(-)/DR-
). The CAFC week 2, 4 and 6 were also enriched in these fractions. These da
ta show that the used CCE procedure is a reliable method to deplete T cells
from stem cell transplants without substantial loss of immature and mature
progenitors.