Allogeneic bone marrow stem cell transplantation following CD34+immunomagnetic enrichment in patients with inherited metabolic storage diseases

被引:23
作者
Gaipa, G
Dassi, M
Perseghin, P
Venturi, N
Corti, P
Bonanomi, S
Balduzzi, A
Longoni, D
Uderzo, C
Biondi, A
Masera, G
Parini, R
Bertagnolio, B
Uziel, G
Peters, C
Rovelli, A
机构
[1] Univ Milano Bicocca, Clin Pediat, Osped S Gerardo, I-20052 Monza, Italy
[2] Osped San Gerardo, Serv Trasfusionale, Unita Aferesi & Criobiol, Monza, Italy
[3] Univ Milan, ICP, Clin Pediat 1, Milan, Italy
[4] Univ Milan, Ist Nazl Neurol C Besta, Milan, Italy
[5] Univ Minnesota, Div Hematol Oncol Blood & Bone Marrow Transplanta, Minneapolis, MN USA
关键词
hematopoietic stem cell transplantation; storage diseases; immunomagnetic enrichment;
D O I
10.1038/sj.bmt.1704024
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
T-cell depletion is an essential step in reducing the risk of graft-versus-host disease (GVHD) in patients with inherited metabolic storage diseases (IMSD) undergoing hematopoietic stem cell transplantation. This goal can be achieved either by selective removal of T cells or by positive selection of CD34 + cells. Large-scale preparations of purified CD34 + cells from bone marrow products have not been extensively described. We report our results with bone marrow C634 + cell enrichment using the CliniMACS system in eight children with IMSD. The median recovery of positively selected CD34 + cells was 46.2% with a purity of 9.5%, and a residual T cell content of 0.04 x 10(6). A median of 5.5 x 10(6)/kg of CD34+ cells was infused. All patients engrafted at a median time of 12 days and none of the patients developed GVHD. This method is technically feasible and can be successfully used to transplant children with IMSD.
引用
收藏
页码:857 / 860
页数:4
相关论文
共 17 条
[1]  
Beaujean F, 1997, TRANSFUS SCI, V18, P251
[2]   COMPARISON OF PURITY AND ENRICHMENT OF CD34(+) CELLS FROM BONE-MARROW, UMBILICAL-CORD AND PERIPHERAL-BLOOD (PRIMED FOR APHERESIS) USING 5 SEPARATION SYSTEMS [J].
DEWYNTER, EA ;
COUTINHO, LH ;
PEI, X ;
MARSH, JCW ;
HOWS, J ;
LUFT, T ;
TESTA, NG .
STEM CELLS, 1995, 13 (05) :524-532
[3]  
GRAINGER J, 2002, BONE MARROW TRANS S2, V29, P30
[4]   Outcome of second hematopoietic cell transplantation in Hurler syndrome [J].
Grewal, SS ;
Krivit, W ;
Defor, TE ;
Shapiro, EG ;
Orchard, PJ ;
Abel, SL ;
Lockman, LA ;
Ziegler, RS ;
Dusenbery, KE ;
Peters, C .
BONE MARROW TRANSPLANTATION, 2002, 29 (06) :491-496
[5]   Transplantation of megadoses of purified haploidentical stem cells [J].
Handgretinger, R ;
Schumm, M ;
Lang, P ;
Greil, J ;
Reiter, A ;
Bader, P ;
Niethammer, D ;
Klingebiel, T .
HEMATOPOIETIC STEM CELLS: BIOLOGY AND TRANSPLANTATION, 1999, 872 :351-362
[6]   Isolation and transplantation of autologous peripheral CD34+ progenitor cells highly purified by magnetic-activated cell sorting [J].
Handgretinger, R ;
Lang, P ;
Schumm, M ;
Taylor, G ;
Neu, S ;
Koscielnak, E ;
Niethammer, D ;
Klingebiel, T .
BONE MARROW TRANSPLANTATION, 1998, 21 (10) :987-993
[7]   The history and future of T-cell depletion as graft-versus-host disease prophylaxis for allogeneic hematopoietic stem cell transplantation [J].
Ho, VT ;
Soiffer, RJ .
BLOOD, 2001, 98 (12) :3192-3204
[8]   BIOCHEMICAL DISCRIMINATION OF HURLER AND SCHEIE SYNDROMES [J].
HOPWOOD, JJ ;
MULLER, V .
CLINICAL SCIENCE, 1979, 57 (03) :265-272
[9]  
KRESSE H, 1982, METHOD ENZYMOL, V83, P559
[10]  
Krivit W, 1999, Curr Opin Neurol, V12, P167, DOI 10.1097/00019052-199904000-00007