Mobilization of hematopoietic progenitor cells in healthy volunteers by AMD3100, a CXCR4 antagonist

被引:596
作者
Liles, WC
Broxmeyer, HE
Rodger, E
Wood, B
Hübel, K
Cooper, S
Hangoc, G
Bridger, GJ
Henson, GW
Calandra, G
Dale, DC
机构
[1] Univ Washington, Dept Med, Seattle, WA 98195 USA
[2] Indiana Univ, Sch Med, Dept Microimmunol, Bloomington, IN 47405 USA
[3] Indiana Univ, Sch Med, Walther Oncol Ctr, Bloomington, IN 47405 USA
[4] Walther Canc Inst, Indianapolis, IN USA
[5] AnorMED Inc, Langley, BC, Canada
关键词
D O I
10.1182/blood-2003-02-0663
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Stromal cell-derived factor 1 (SDF1/CXCL12 ) and its cognate receptor, CXCR4, play key regulatory roles in CD34(+) cell trafficking. We investigated whether AMD3100, a selective CXCR14 antagonist, could mobilize hematopoietic progenitor cells from marrow to peripheral blood in healthy human volunteers. Initially, 10 persons each received a single dose of AMD3100 (80 mug/kg subcutaneously), which induced rapid, generalized leukocytosis associated with an increase in peripheral blood CD34(+) cells, representing pluripotent hematopoietic progenitors by in vitro colony-forming unit assays, from 3.8 +/- 0.5/muL to 20.7 +/- 3.5/muL at 6 hours. Subsequent dose-response studies showed a maximum increase in circulating CD34(+) cells from 2.6 +/- 0.3/muL to 40.4 +/- 3.4/muL at 9 hours after 240 mug/kg AMD3100. Serial administration of AMD3100 (80 mug/kg/d for 3 days) resulted in consistent, reversible increases in peripheral blood CD34(+) cells. AMD3100 was well tolerated and caused only mild, transient toxicity. These findings suggest potential clinical application of AMD3100 for CD34(+) cell mobilization and collection for hematopoietic stem cell transplantation. (C) 2003 by The American Society of Hematology.
引用
收藏
页码:2728 / 2730
页数:3
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