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
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作者:
Liles, WC
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机构:Univ Washington, Dept Med, Seattle, WA 98195 USA
Liles, WC
Rodger, E
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机构:Univ Washington, Dept Med, Seattle, WA 98195 USA
Rodger, E
Broxmeyer, HE
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机构:Univ Washington, Dept Med, Seattle, WA 98195 USA
Broxmeyer, HE
Dehner, C
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机构:Univ Washington, Dept Med, Seattle, WA 98195 USA
Dehner, C
Badel, K
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机构:Univ Washington, Dept Med, Seattle, WA 98195 USA
Badel, K
Calandra, G
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机构:Univ Washington, Dept Med, Seattle, WA 98195 USA
Calandra, G
Christensen, J
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机构:Univ Washington, Dept Med, Seattle, WA 98195 USA
Christensen, J
Wood, B
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机构:Univ Washington, Dept Med, Seattle, WA 98195 USA
Wood, B
Price, TH
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机构:Univ Washington, Dept Med, Seattle, WA 98195 USA
Price, TH
Dale, DC
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机构:Univ Washington, Dept Med, Seattle, WA 98195 USA
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
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.
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Barlogie, B
Shaughnessy, J
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Shaughnessy, J
Tricot, G
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Tricot, G
Jacobson, J
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Jacobson, J
Zangari, M
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Zangari, M
Anaissie, E
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Anaissie, E
Walker, R
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Walker, R
Crowley, J
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Barlogie, B
Shaughnessy, J
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机构:
Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Shaughnessy, J
Tricot, G
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Tricot, G
Jacobson, J
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Jacobson, J
Zangari, M
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Zangari, M
Anaissie, E
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Anaissie, E
Walker, R
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
Walker, R
Crowley, J
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Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USAUniv Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA