Autologous peripheral blood progenitor cell transplantation.
Autologous peripheral blood progenitor cell transplantation.
复制标题
自体外周血祖细胞移植。
DOI:
10.1002/jca.2920100307
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发表时间:
1995
期刊:
影响因子:
--
通讯作者:
Anderson,KC
中科院分区:
文献类型:
--
作者:
Anderson,KC
Harvesting of autologous peripheral blood stem cells (PBSCs) has been facilitated by using currently available, efficient apheresis technology at the time of rebound from chemotherapy while patients are receiving recombinant growth factors, i.e., granulocyte (G) or granulocyte‐macrophage (GM) colony stimulating factor (CSF). Ideally pheresis should be done before patients have had extensive stem cell toxins, i.e., alkylating agents or nitrosoureas. This strategy has facilitated the use of high dose chemoradiotherapy given as a single regimen or in a divided dose for patients with solid tumors or hematologic malignancies and results in more rapid engraftment than bone marrow transplantation (BMT). Although mere are no assays which measure repopulating stem cells, enumeration of CD34+cells within PBSCs is a direct and rapid assay which provides an index of both early and late long‐term reconstitutive capacity, since it correlates with colony‐forming unit (CFU)‐GMs, as well as pre‐progenitor or delta assays and long‐term culture‐initiating cells (LTC‐IC). A threshold of ≥2 × 106CD34+cells/kg recipient body weight has been reported to be required for engraftment, but may vary depending upon the clinical setting. Strategies for mobilization of normal PBSCs also increase tumor cell contamination within PB in the setting of both hematologic malignancies and solid tumors, but the significance of these tumor cells in terms of patient outcome is unclear. Recently isolation of CD34+cells from PBSCs has been done using magnetic beads or immunoabsorption on columns or rigid plates in order to enrich for normal hematopoietic progenitors and potentially decrease tumor cell contamination. As for other cellular blood components, standards have been developed to assure efficient collection and processing, thawing, and reinfusion, and to maintain optimal PBPC viability. Finally, future directions of clinical research include expansion of hematopoietic progenitor cells ex vivo; use of umbilical cord or placenta as rich sources of progenitor cells; syngeneic hematopoietic stem cell transplantation; related and unrelated allogeneic hematopoietic stem cell transplantation; treatment of infections, i.e., Epstein Barr virus, or tumor relapse after allogeneic BMT using donor PBSC infusions; and gene therapy approaches.
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影响因子:
20.3
作者:
M. Dimopoulos;R. Alexanian;D. Przepiorka;J. Hester;B. Andersson;S. Giralt;R. Mehra;K. V. Besien;K. Delasalle;C. Reading
通讯作者:
C. Reading
影响因子:
20.3
作者:
G. Tricot;S. Jagannath;D. Vesole;J. Nelson;S. Tindle;L. Miller;B. Cheson;J. Crowley;B. Barlogie
通讯作者:
G. Tricot;S. Jagannath;D. Vesole;J. Nelson;S. Tindle;L. Miller;B. Cheson;J. Crowley;B. Barlogie
影响因子:
20.3
作者:
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通讯作者:
J. Brouet
影响因子:
20.3
作者:
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通讯作者:
J. Berenson
影响因子:
20.3
作者:
W. Brugger;R. Henschler;S. Heimfeld;R. Berenson;R. Mertelsmann;Lothar Kanz
通讯作者:
Lothar Kanz