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dc.contributor.authorPettengell, Ruth
dc.contributor.authorWoll, Penella J
dc.contributor.authorChang, James
dc.contributor.authorCoutinho, Lucia H
dc.contributor.authorTesta, Nydia G
dc.contributor.authorCrowther, Derek
dc.date.accessioned2010-04-26T13:26:30Z
dc.date.available2010-04-26T13:26:30Z
dc.date.issued1994-07
dc.identifier.citationEffects of erythropoietin on mobilisation of haemopoietic progenitor cells. 1994, 14 (1):125-30 Bone Marrow Transplant.en
dc.identifier.issn0268-3369
dc.identifier.pmid7951099
dc.identifier.urihttp://hdl.handle.net/10541/97389
dc.description.abstractPeripheral blood progenitor cell (PBPC) mobilising regimens that do not include cytotoxic drugs are needed if PBPC are to be used for allogeneic transplantation. We have studied the effects of erythropoietin on bone marrow and circulating haemopoietic progenitors. Eleven patients with untreated lymphoma received epoetin-alpha 300 or 450 iu/kg subcutaneously (sc) thrice weekly for 2 weeks. Their bone marrows and peripheral bloods were normal at entry. There were no differences between dose levels. Peripheral blood colony-forming cell (CFC) numbers increased fivefold over baseline (p = 0.003) including a sevenfold increase in GM-CFC (p = 0.003). CD34-positive cell numbers increased 4.6-fold (P < 0.01). Maximal CFC release was seen at days 5-8. No consistent change in megakaryocyte numbers was seen. The increase in numbers of cells capable of long-term haemopoiesis was not significant. The ratio of myeloid:erythroid cells in bone marrow reduced from 2.7 to 0.86 after erythropoietin treatment (p = 0.047). In bone marrow the only significant rise in CFCs was in erythroid progenitors. Erythropoietin alone resulted in a modest increase in PBPC that is unlikely to be useful for transplantation. The effects of erythropoietin in combination with other cytokines or with cytotoxic drugs remain to be explored.
dc.language.isoenen
dc.subjectHaematopoiesisen
dc.subjectHaematopoietic Stem Cell Transplantationen
dc.subjectHaematopoietic Stem Cellsen
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshBone Marrow
dc.subject.meshColony-Forming Units Assay
dc.subject.meshErythropoietin
dc.subject.meshFemale
dc.subject.meshHematopoiesis
dc.subject.meshHematopoietic Stem Cell Transplantation
dc.subject.meshHematopoietic Stem Cells
dc.subject.meshHodgkin Disease
dc.subject.meshHumans
dc.subject.meshLymphoma, Non-Hodgkin
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshRecombinant Proteins
dc.subject.meshTransplantation, Autologous
dc.titleEffects of erythropoietin on mobilisation of haemopoietic progenitor cells.en
dc.typeArticleen
dc.contributor.departmentDepartment of Medical Oncology, Christie Hospital, Manchester, UK.en
dc.identifier.journalBone Marrow Transplantationen
html.description.abstractPeripheral blood progenitor cell (PBPC) mobilising regimens that do not include cytotoxic drugs are needed if PBPC are to be used for allogeneic transplantation. We have studied the effects of erythropoietin on bone marrow and circulating haemopoietic progenitors. Eleven patients with untreated lymphoma received epoetin-alpha 300 or 450 iu/kg subcutaneously (sc) thrice weekly for 2 weeks. Their bone marrows and peripheral bloods were normal at entry. There were no differences between dose levels. Peripheral blood colony-forming cell (CFC) numbers increased fivefold over baseline (p = 0.003) including a sevenfold increase in GM-CFC (p = 0.003). CD34-positive cell numbers increased 4.6-fold (P < 0.01). Maximal CFC release was seen at days 5-8. No consistent change in megakaryocyte numbers was seen. The increase in numbers of cells capable of long-term haemopoiesis was not significant. The ratio of myeloid:erythroid cells in bone marrow reduced from 2.7 to 0.86 after erythropoietin treatment (p = 0.047). In bone marrow the only significant rise in CFCs was in erythroid progenitors. Erythropoietin alone resulted in a modest increase in PBPC that is unlikely to be useful for transplantation. The effects of erythropoietin in combination with other cytokines or with cytotoxic drugs remain to be explored.


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