Transplantation of hematopoietic stem cells from the peripheral blood

被引:72
作者
Jansen, J [1 ]
Hanks, S [1 ]
Thompson, JM [1 ]
Dugan, MJ [1 ]
Akard, LP [1 ]
机构
[1] Indiana Blood & Marrow Transplantat, Beech Grove, IN 46107 USA
关键词
stem-cell transplantation; CD34; colony-forming unit granulocyte macrophage; CFU-GM; mobilization;
D O I
10.1111/j.1582-4934.2005.tb00335.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hematopoietic stem cells can be collected from the peripheral blood. These hematopoietic stem cells (HSC), or better progenitor cells, are mostly expressed as the percentage of cells than react with CD34 antibodies or that form colonies in semi-solid medium (CFU-GM). Under steady-state conditions the number of HSC is much lower in peripheral blood than in bone marrow. Mobilization with chemotherapy and/or growth factors may lead to a concentration of HSC in the peripheral blood that equals or exceeds the concentration in bone marrow. Transplantation of HSC from the peripheral blood results in faster hematologic recovery than HSC from bone marrow. This decreases the risk of infection and the need for blood-product support. For autologous stem-cell transplantation (SCT), the use of peripheral blood cells has completely replaced the use of bone marrow. For allogeneic SCT, on the other hand, the situation is more complex. Since peripheral blood contains more T-lymphocytes than bone marrow, the use of HSC from the peripheral blood increases the risk of graft-versus-host disease after allogencic SCT. For patients with good-risk leukemia, bone marrow is still preferred, but for patients with high-risk disease, peripheral blood SCT has become the therapy of choice.
引用
收藏
页码:37 / 50
页数:14
相关论文
共 63 条
[21]   Immunobiology of allogeneic peripheral blood mononuclear cells mobilized with granulocyte-colony stimulating factor [J].
Gyger, M ;
Stuart, RK ;
Perreault, C .
BONE MARROW TRANSPLANTATION, 2000, 26 (01) :1-16
[22]   CAMPATH-1 antibodies in stem-cell transplantation [J].
Hale, G ;
Cobbold, S ;
Novitzky, N ;
Bunjes, D ;
Willemze, R ;
Prentice, HG ;
Milligan, D ;
Mackinnon, S ;
Waldmann, H .
CYTOTHERAPY, 2001, 3 (03) :145-164
[23]  
Ho AD, 1996, EXP HEMATOL, V24, P1460
[24]   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
[25]   Survival after HLA-identical allogeneic peripheral blood stem cell and bone marrow transplantation for hematologic malignancies: meta-analysis of randomized controlled trials [J].
Horan, JT ;
Liesveld, JL ;
Fernandez, ID ;
Lyman, GH ;
Phillips, GL ;
Lerner, NB ;
Fisher, SG .
BONE MARROW TRANSPLANTATION, 2003, 32 (03) :293-298
[26]  
JACOBSON LO, 1949, J LAB CLIN MED, V34, P1538
[27]   Impaired PBPC collection in patients with myeloma after high-dose melphalan [J].
Jansen, J ;
Thompson, JM ;
Dugan, MJ ;
Wiemann, MC ;
Hanks, S ;
Greenspan, AR ;
Akard, LP .
CYTOTHERAPY, 2004, 6 (05) :498-504
[28]   Peripheral blood progenitor cell transplantation [J].
Jansen, J ;
Thompson, JM ;
Dugan, MJ ;
Nolan, P ;
Wiemann, MC ;
Birhiray, R ;
Henslee-Downey, PJ ;
Akard, LP .
THERAPEUTIC APHERESIS, 2002, 6 (01) :5-14
[29]  
JANSEN J, 1983, EXP HEMATOL, V11, P967
[30]  
KESSINGER A, 1989, BONE MARROW TRANSPL, V4, P643