Allogeneic peripheral blood stem cell transplantation following CD34+ enrichment by density gradient separation

被引:7
|
作者
Vij, R
Brown, R
Shenoy, S
Haug, JS
Kaesberg, D
Adkins, D
Goodnough, LT
Khoury, H
DiPersio, J
机构
[1] Washington Univ, Sch Med, Div Bone Marrow Transplantat & Stem Cell Biol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pediat Hematol, St Louis, MO 63110 USA
关键词
CD34; selection; allogeneic transplantation; GVHD; dendritic cells; cytokines;
D O I
10.1038/sj.bmt.1702427
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
GVHD is a significant cause of morbidity and mortality following allogeneic peripheral blood stem cell transplantation (AlloPBSC). CD34(+) cell selection could reduce GVHD by negative selection of T cells. In an attempt to reduce the T cell content of alloPBSC we carried out a trial in which 11 patients with hematologic malignancies received alloPBSC from HLA-matched siblings following density gradient separation using an isotonic colloidal silica solution (BDS 60; Dendreon Corporation). Cyclosporine and methylprednisone were used for GVHD prophylaxis. The mean yield of CD34(+) cells was 69 +/- 15.6% with a purity of 2.9 +/- 1.7%. The mean number of CD3(+) cells infused was 1.0 +/- 1.2 x 10(7)/kg, representing a 1.3 log depletion. A high risk of acute GVHD was observed: grade II-IV in 7/11 (64%) and grade III-IV GVHD in 5/11 (45%) patients. Nine of the 11 (82%) patients died with a median survival of 68 days. Cytokine expression in PBSC was compared pre and post processing. Interferon-gamma was detected only following density gradient separation while IL-8 expression increased 3- to 6-fold post processing. Therefore, processing with this device may augment production of pro-inflammatory cytokines.
引用
收藏
页码:1223 / 1228
页数:6
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