Improved immunomagnetic enrichment of CD34+ cells from umbilical cord blood using the CliniMACS cell separation system

被引:5
作者
Blake, Joseph M. [1 ]
Nicoud, Ian B. [1 ]
Weber, Daniel [1 ]
Voorhies, Howard [1 ]
Guthrie, Katherine A. [1 ]
Heimfeld, Shelly [1 ]
Delaney, Colleen [1 ,2 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
[2] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
CD34; CliniMACS; cord blood; enrichment; immunomagnetic selection; HEMATOPOIETIC STEM-CELLS; EX-VIVO EXPANSION; PROGENITOR CELLS; TRANSPLANTATION; ENGRAFTMENT;
D O I
10.3109/14653249.2012.681040
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background aims. CD34(+) enrichment from cord blood units (CBU) is used increasingly in clinical applications involving ex vivo expansion. The CliniMACS instrument from Miltenyi Biotec is a current good manufacturing practice (cGMP) immunomagnetic selection system primarily designed for processing larger numbers of cells: a standard tubing set (TS) can process a maximum of 60 billion cells, while the larger capacity tubing set (LS) will handle 120 billion cells. In comparison, most CBU contain only 1-2 billion cells, raising a question regarding the optimal tubing set for CBU CD34(+) enrichment. We compared CD34(+) cell recovery and overall viability after CliniMACS processing of fresh CBU with either TS or LS. Methods. Forty-six freshly collected CBU (<= 36 h) were processed for CD34(+) enrichment; 22 consecutive units were selected using TS and a subsequent 24 processed with LS. Cell counts and immunophenotyping were performed pre- and post-selection to assess total nucleated cells (TNC), viability and CD34(+) cell content. Results. Two-sample t-tests of mean CD34(+) recovery and viability revealed significant differences in favor of LS (CD34(+) recovery, LS = 56%, TS = 45%, P = 0.003; viability, LS = 74%, TS = 59%, P = 0.011). Stepwise linear regression, considering pre-processing unit age, viability, TNC and CD34+ purity, demonstrated statistically significant correlations only with the tubing set used and age of unit. Conclusions. For CD34(+) enrichment from fresh CBU, LS provided higher post-selection viability and more efficient recovery. In this case, a lower maximum TNC specification of TS was not predictive of better performance. The same may hold for smaller scale enrichment of other cell types with the CliniMACS instrument.
引用
收藏
页码:818 / 822
页数:5
相关论文
共 12 条
[1]   Allogeneic hematopoietic cell transplantation for hematologic malignancy: relative risks and benefits of double umbilical cord blood [J].
Brunstein, Claudio G. ;
Gutman, Jonathan A. ;
Weisdorf, Daniel J. ;
Woolfrey, Ann E. ;
DeFor, Todd E. ;
Gooley, Theodore A. ;
Verneris, Michael R. ;
Appelbaum, Frederick R. ;
Wagner, John E. ;
Delaney, Colleen .
BLOOD, 2010, 116 (22) :4693-4699
[2]   Ex vivo expansion of human hematopoietic stem and progenitor cells [J].
Dahlberg, Ann ;
Delaney, Colleen ;
Bernstein, Irwin D. .
BLOOD, 2011, 117 (23) :6083-6090
[3]   Strategies to enhance umbilical cord blood stem cell engraftment in adult patients [J].
Delaney, Colleen ;
Ratajczak, Mariusz Z. ;
Laughlin, Mary J. .
EXPERT REVIEW OF HEMATOLOGY, 2010, 3 (03) :273-283
[4]   Notch-mediated expansion of human cord blood progenitor cells capable of rapid myeloid reconstitution [J].
Delaney, Colleen ;
Heimfeld, Shelly ;
Brashem-Stein, Carolyn ;
Voorhies, Howard ;
Manger, Ronald L. ;
Bernstein, Irwin D. .
NATURE MEDICINE, 2010, 16 (02) :232-U143
[5]   Refreezing of cord blood hematopoietic stem cells for allogenic transplantation: in vitro and in vivo validation of a clinical phase I/II protocol in European and Italian Good Manufacturing Practice conditions [J].
Gunetti, Monica ;
Ferrero, Ivana ;
Rustichelli, Deborah ;
Berger, Massimo ;
Gammaitoni, Loretta ;
Timeus, Fabio ;
Piacibello, Wanda ;
Aglietta, Massimo ;
Fagioli, Franca .
EXPERIMENTAL HEMATOLOGY, 2008, 36 (02) :235-243
[6]  
Ko KH, 2011, METHODS MOL BIOL, V761, P249, DOI 10.1007/978-1-61779-182-6_17
[7]   Simultaneous cord blood transplantation of ex vivo expanded together with non-expanded cells for high risk leukemia [J].
Kögler, G ;
Nürnberger, W ;
Fischer, J ;
Niehues, T ;
Somville, T ;
Göbel, U ;
Wernet, P .
BONE MARROW TRANSPLANTATION, 1999, 24 (04) :397-403
[8]   Clinically relevant expansion of hematopoietic stem cells with conserved function in a single-use, closed-system bioprocess [J].
Madlambayan, Gerard J. ;
Rogers, Ian ;
Purpura, Kelly A. ;
Ito, Caryn ;
Yu, Mei ;
Kirouac, Daniel ;
Casper, Robert F. ;
Zandstra, Peter W. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2006, 12 (10) :1020-1030
[9]  
Miltenyi Biotec GmbH, 2006, CLINIMACS US MAN US
[10]   Superior ex vivo cord blood expansion following co-culture with bone marrow-derived mesenchymal stem cells [J].
Robinson, SN ;
Ng, J ;
Niu, T ;
Yang, H ;
McMannis, JD ;
Karandish, S ;
Kaur, I ;
Fu, P ;
Del Angel, M ;
Messinger, R ;
Flagge, F ;
de Lima, M ;
Decker, W ;
Xing, D ;
Champlin, R ;
Shpall, EJ .
BONE MARROW TRANSPLANTATION, 2006, 37 (04) :359-366