Combined positive and negative cell selection from allogeneic peripheral blood progenitor cells (PBPC) by use of immunomagnetic methods

Citation
Ga. Martin-henao et al., Combined positive and negative cell selection from allogeneic peripheral blood progenitor cells (PBPC) by use of immunomagnetic methods, BONE MAR TR, 27(7), 2001, pp. 683-687
Citations number
20
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
Journal title
BONE MARROW TRANSPLANTATION
ISSN journal
02683369 → ACNP
Volume
27
Issue
7
Year of publication
2001
Pages
683 - 687
Database
ISI
SICI code
0268-3369(200104)27:7<683:CPANCS>2.0.ZU;2-S
Abstract
Twenty-four mobilized peripheral blood products from healthy donors for all ogeneic transplantation were positively selected for CD34(+) cells and depl eted of CD4(+) and CD8(+) cells (+/- selection) by combining clinical grade immunomagnetic methods. A sequential, 'two-step' strategy combining positi ve selection of CD34(+) cells by use of the Isolex 300i (versions 1 and 2) device and T cell depletion (TCD) using the MaxSep device and a simultaneou s, 'one-step' method of CD34(+) cell selection and TCD using the Isolex 300 i (software versions 1 and 2) have been investigated. Using these magnetic bead separation systems, two groups of sequential +/- selection (Isolex 300 i version 1/MaxSep and Isolex 300i version 2/MaxSep) and two groups of simu ltaneous +/- selection (Isolex 300i versions 1 and 2) were analysed, In the sequential +/- selection, logarithms of TCD (CD3(+) cell depletion) obtain ed by the positive selection step had median values of 3.7 with the version 1 (n = 5) and 4.5 with version 2 software of the Isolex 300i (n = 5) (P = 0.07), Version 2 also gave a higher CD34(+) cell purity and yield than did version 1 (92% vs 77%, P < 0.05 and 55% vs 34%, P = 0.3, respectively), Add itional TCD obtained in the second step with the MaxSep device for the two groups had a median value of 0.9 log and 7% CD34(+) cell losses. In the sim ultaneous +/- selection, the Isolex 300i version 2 (n = 10) gave a median T CD of 5.1 log and version 1 (n = 4) of 4 log (P < 0.005), Higher CD34(+) ce ll purity and yield were also obtained with version 2 than with version 1 ( 97% and 76%, P < 0.005 and 57% and 39%, P = 0.07, respectively). These data indicate that simultaneous, 'one-step' +/- selection in the Isolex 300i ve rsion 2 achieves a high TCD with a high CD34(+) cell purity and an acceptab le CD34(+) cell yield.