Enumeration of bone marrow 'homing' haemopoietic stem cells from G-CSF-mobilised normal donors and influence on engraftment following allogeneic transplantation

被引:25
作者
Spencer, A [1 ]
Jackson, J [1 ]
Baulch-Brown, C [1 ]
机构
[1] Alfred Hosp, BMT Programme, Melbourne, Vic, Australia
关键词
CXCR4; allogeneic transplant; engraftment;
D O I
10.1038/sj.bmt.1703289
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Expression of the chemokine receptor CXCR4 on human haemopoietic stem cells (HSC) may play a crucial role in localising these cells to the bone marrow. To evaluate whether CXCR4 expression is clinically relevant we have enumerated CXCR4-positive HSC used for allogeneic transplantation and sought any relationship with the rate of subsequent haemopoietic reconstitution. CD34-positive progenitor cells were isolated from peripheral blood stem cell (PBSC) collections from 16 normal donors. The proportion of cells co-expressing CXCR4 was enumerated and the times to recipient haemopoietic reconstitution measured. The median frequency of CD34-positive cells co-expressing CXCR4 was 41% (range 16% to 76%) and the median number of CXCR4 CD34 double-positive cells infused at transplantation was 2.5 x 10(6) cells/kg (range 0.8-10.3). Patients receiving >2.5 x 10(6) CXCR4 CD34 double-positive cells/kg demonstrated a significant shortening of time to platelet engraftment compared to the recipients of the lower cell doses (10 days vs 14.5 days, respectively, P = 0.02) with all but one of the recipients of the higher cell doses achieving platelet engraftment by day 11. Coexpression of CXCR4 on CD34-positive progenitor cells may be an important determinant of post-transplant engraftment and in our hands transplantation of a minimum of 2.5 x 10(6) CXCR4 CD34 double-positive cells/kg ensured rapid post-transplant platelet recovery.
引用
收藏
页码:1019 / 1022
页数:4
相关论文
共 12 条
[1]   The chemokine SDF-1 is a chemoattractant for human CD34(+) hematopoietic progenitor cells and provides a new mechanism to explain the mobilization of CD34(+) progenitors to peripheral blood [J].
Aiuti, A ;
Webb, IJ ;
Bleul, C ;
Springer, T ;
GutierrezRamos, JC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (01) :111-120
[2]   Purification of primitive human hematopoietic cells capable of repopulating immune-deficient mice [J].
Bhatia, M ;
Wang, JCY ;
Kapp, U ;
Bonnet, D ;
Dick, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5320-5325
[3]  
DEOGYEON J, 2000, J CLIN INVEST, V105, P101
[4]   High CD34+ cell counts decrease hematologic toxicity of autologous peripheral blood progenitor cell transplantation [J].
Ketterer, N ;
Salles, G ;
Raba, M ;
Espinouse, D ;
Sonet, A ;
Tremisi, P ;
Dumontet, C ;
Moullet, I ;
Eljaafari-Corbin, A ;
Neidhardt-Berard, EM ;
Bouafia, F ;
Coiffier, B .
BLOOD, 1998, 91 (09) :3148-3155
[5]   The chemokine receptor CXCR-4 is expressed on CD34+ hematopoietic progenitors and leukemic cells and mediates transendothelial migration induced by stromal cell-derived factor-1 [J].
Möhle, R ;
Bautz, F ;
Rafii, S ;
Moore, MAS ;
Brugger, W ;
Kanz, L .
BLOOD, 1998, 91 (12) :4523-4530
[6]   Dependence of human stem cell engraftment and repopulation of NOD/SCID mice on CXCR4 [J].
Peled, A ;
Petit, I ;
Kollet, O ;
Magid, M ;
Ponomaryov, T ;
Byk, T ;
Nagler, A ;
Ben-Hur, H ;
Many, A ;
Shultz, L ;
Lider, O ;
Alon, R ;
Zipori, D ;
Lapidot, T .
SCIENCE, 1999, 283 (5403) :845-848
[7]   The human hematopoietic stem cell compartment is heterogeneous for CXCR4 expression [J].
Rosu-Myles, M ;
Gallacher, L ;
Murdoch, B ;
Hess, DA ;
Keeney, M ;
Kelvin, D ;
Dale, L ;
Ferguson, SSG ;
Wu, DM ;
Fellows, F ;
Bhatia, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) :14626-14631
[8]  
Sutherland D R, 1996, J Hematother, V5, P213, DOI 10.1089/scd.1.1996.5.213
[9]   The biology and clinical uses of blood stem cells [J].
To, LB ;
Haylock, D ;
Simmons, PJ ;
Juttner, CA .
BLOOD, 1997, 89 (07) :2233-2258
[10]  
TRICOT G, 1995, BLOOD, V85, P588