Mobilization of hematopoietic stem cells into the peripheral blood

被引:8
作者
Damon, Lloyd E. [1 ]
Damon, Lauren E. [2 ]
机构
[1] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[2] Johns Hopkins Univ, Baltimore, MD USA
关键词
chemotherapy; CXCR4-CXCL12; hematopoietic stem cell; mobilization; mobilization failure; osteoblast; plerixafor; COLONY-STIMULATING FACTOR; AUTOLOGOUS BONE-MARROW; HIGH-DOSE CYCLOPHOSPHAMIDE; NON-HODGKINS-LYMPHOMA; PLUS G-CSF; HUMAN MEGAKARYOCYTE GROWTH; TERM REPOPULATING ABILITY; C-MPL LIGAND; PROGENITOR CELLS; MULTIPLE-MYELOMA;
D O I
10.1586/EHM.09.54
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hematopoietic stem cells can be mobilized out of the bone marrow into the blood for the reconstitution of hematopoiesis following high-dose therapy. Methods to improve mobilization efficiency and yields are rapidly emerging. Traditional methods include chemotherapy with or without myeloid growth factors. Plerixafor, a novel agent that disrupts the CXCR4-CXCL12 bond, the primary hematopoietic stem cell anchor in the bone marrow, has recently been US FDA-approved for mobilizing hematopoietic stem cells in patients with non-Hodgkin lymphoma and multiple myeloma. Plerixafor and myeloid growth factors as single agents appear safe to use in family or volunteer hematopoietic stem cells donors. Plerixafor mobilizes leukemic stem cells and is not approved for use in patients with acute leukemia. Patients failing to mobilize adequate hematopoietic stem cells with myeloid growth factors can often be successfully mobilized with chemotherapy plus myeloid growth factors or with plerixafor and granulocyte colony-stimulating factor.
引用
收藏
页码:717 / 733
页数:17
相关论文
共 176 条
[1]   The hematopoietic stem cell in its place [J].
Adams, GB ;
Scadden, DT .
NATURE IMMUNOLOGY, 2006, 7 (04) :333-337
[2]   Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor [J].
Center for Regenerative Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, United States ;
不详 ;
不详 ;
不详 ;
不详 ;
不详 .
Nature, 2006, 7076 (599-603) :599-603
[3]   Pharmacokinetics and adverse events following 5-day repeated administration of lenograstim, a recombinant human granulocyte colony-stimulating factor, in healthy subjects [J].
Akizuki, S ;
Mizorogi, F ;
Inoue, T ;
Sudo, K ;
Ohnishi, A .
BONE MARROW TRANSPLANTATION, 2000, 26 (09) :939-946
[4]   Long-term follow-up of normal peripheral blood progenitor cell donors treated with filgrastim:: no evidence of increased risk of leukemia development [J].
Anderlini, P ;
Chan, FA ;
Champlin, RE ;
Körbling, M ;
Strom, SS .
BONE MARROW TRANSPLANTATION, 2002, 30 (10) :661-663
[5]   Clinical toxicity and laboratory effects of granulocyte-colony-stimulating factor (filgrastim) mobilization and blood stem cell apheresis from normal donors, and analysis of charges for the procedures [J].
Anderlini, P ;
Przepiorka, D ;
Seong, D ;
Miller, P ;
Sundberg, J ;
Lichtiger, B ;
Norfleet, F ;
Chan, KW ;
Champlin, R ;
Korbling, M .
TRANSFUSION, 1996, 36 (07) :590-595
[6]   Peripheral blood stem cell donation: an analysis from the International Bone Marrow Transplant Registry (IBMTR) and European Group for Blood and Marrow Transplant (EBMT) databases [J].
Anderlini, P ;
Rizzo, JD ;
Nugent, ML ;
Schmitz, N ;
Champlin, RE ;
Horowitz, MM .
BONE MARROW TRANSPLANTATION, 2001, 27 (07) :689-692
[7]   A model of in vivo purging with Rituximab and high-dose AraC in follicular and mantle cell lymphoma [J].
Arcaini, L ;
Orlandi, E ;
Alessandrino, EP ;
Iacona, I ;
Brusamolino, E ;
Bonfichi, M ;
Bernasconi, P ;
Calatroni, S ;
Tenore, A ;
Montanari, F ;
Troletti, D ;
Pascutto, C ;
Regazzi, M ;
Lazzarino, M .
BONE MARROW TRANSPLANTATION, 2004, 34 (02) :175-179
[8]   BONE-MARROW TRANSPLANTATION [J].
ARMITAGE, JO .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (12) :827-838
[9]   Randomized comparison of granulocyte colony-stimulating factor versus granulocyte-macrophage colony-stimulating factor plus intensive chemotherapy for peripheral blood stem cell mobilization and autologous transplantation in multiple myeloma [J].
Arora, M ;
Burns, LJ ;
Barker, JN ;
Miller, JS ;
Defor, TE ;
Olujohungbe, AB ;
Weisdorf, DJ .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2004, 10 (06) :395-404
[10]   What is the true nature of the osteoblastic hematopoietic stem cell niche? [J].
Askmyr, Maria ;
Sims, Natalie A. ;
Martin, T. John ;
Purton, Louise E. .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2009, 20 (06) :303-309