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

Citation
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
Journal title
BONE MARROW TRANSPLANTATION
ISSN journal
02683369 → ACNP
Volume
23
Issue
10
Year of publication
1999
Pages
1061 - 1070
Database
ISI
SICI code
0268-3369(199905)23:10<1061:CCAAOA>2.0.ZU;2-V
Abstract
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.