Augmented mobilization and collection of CD34+ hematopoietic cells from normal human volunteers stimulated with granulocyte-colony-stimulating factor by single-dose administration of AMD3100, a CXCR4 antagonist

被引:179
作者
Liles, WC
Rodger, E
Broxmeyer, HE
Dehner, C
Badel, K
Calandra, G
Christensen, J
Wood, B
Price, TH
Dale, DC
机构
[1] Univ Washington, Dept Med, Seattle, WA 98195 USA
[2] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
[4] Walther Canc Inst, Indianapolis, IN USA
[5] AnorMed Inc, Langley, BC, Canada
[6] Puget Sound Blood Ctr, Seattle, WA 98104 USA
关键词
D O I
10.1111/j.1537-2995.2005.04222.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: AMD3100, a selective antagonist of CXCR4, rapidly mobilizes CD34+ hematopoietic progenitor cells (HPCs) from marrow to peripheral blood with minimal side effects. STUDY DESIGN AND METHODS: To further investigate potential clinical utility of AMD3100 for CD34+ cell mobilization and collection, a Phase I study in normal volunteers was performed examining single-dose administration of AMD3100 alone and in combination with a standard 5-day granulocyte-colony-stimulating factor (G-CSF) regimen. RESULTS: AMD3100 (160 mu g/kg x 1 on Day 5) significantly increased both G-CSF-stimulated (10 mu g/kg/ day) mobilization of CD34+ cells (3.8-fold) and leukapheresis yield of CD34+ cells. Moreover, collection of CD34+ cells was comparable between individuals mobilized by a single-dose regimen of AMD3100 (240 mu g/ kg) and individuals mobilized with a 5-day regimen of G-CSF AMD3100-mobilized leukapheresis products contained significantly greater numbers of T and B cells compared to G-CSF-stimulated leukapheresis products. CONCLUSION: These findings indicate that AMD3100 can be used alone or as an adjunct to G-CSF to mobilize cells for HPC transplantation.
引用
收藏
页码:295 / 300
页数:6
相关论文
共 38 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
    Aiuti, A
    Webb, IJ
    Bleul, C
    Springer, T
    GutierrezRamos, JC
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (01) : 111 - 120
  • [2] Anderlini P, 1997, BLOOD, V90, P903
  • [3] Allogeneic blood progenitor cell collection in normal donors after mobilization with filgrastim:: the M.D. Anderson Cancer Center experience
    Anderlini, P
    Donato, M
    Chan, KW
    Huh, YO
    Gee, AP
    Lauppe, MJ
    Champlin, RE
    Körbling, M
    [J]. TRANSFUSION, 1999, 39 (06) : 555 - 560
  • [4] Barille-Nion Sophie, 2003, Hematology Am Soc Hematol Educ Program, P248
  • [5] Treatment of multiple myeloma
    Barlogie, B
    Shaughnessy, J
    Tricot, G
    Jacobson, J
    Zangari, M
    Anaissie, E
    Walker, R
    Crowley, J
    [J]. BLOOD, 2004, 103 (01) : 20 - 32
  • [6] FACTORS THAT INFLUENCE COLLECTION AND ENGRAFTMENT OF AUTOLOGOUS PERIPHERAL-BLOOD STEM-CELLS
    BENSINGER, W
    APPELBAUM, F
    ROWLEY, S
    STORB, R
    SANDERS, J
    LILLEBY, K
    GOOLEY, T
    DEMIRER, T
    SCHIFFMAN, K
    WEAVER, C
    CLIFT, R
    CHAUNCEY, T
    KLARNET, J
    MONTGOMERY, P
    PETERSDORF, S
    WEIDEN, P
    WITHERSPOON, R
    BUCKNER, CD
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (10) : 2547 - 2555
  • [7] Factors that influence the collection and engraftment of allogeneic peripheral-blood stem cells in patients with hematologic malignancies
    Brown, RA
    Adkins, D
    Goodnough, LT
    Haug, JS
    Todd, G
    Wehde, M
    Hendricks, D
    Ehlenbeck, C
    Laub, L
    DiPersio, J
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (09) : 3067 - 3074
  • [8] Cottler-Fox Michele H, 2003, Hematology Am Soc Hematol Educ Program, P419
  • [9] Dale DC, 2003, BLOOD, V102, p38A
  • [10] An evaluation of predictive factors for CD34+cell harvest yields from patients mobilized with chemotherapy and growth factors
    Ford, CD
    Chan, KJ
    Reilly, WF
    Petersen, FB
    [J]. TRANSFUSION, 2003, 43 (05) : 622 - 625