CD34 positive PBPC expanded ex vivo may not provide durable engraftment following myeloablative chemoradiotherapy regimens

We have previously demonstrated that CD34+ cells, selected from peripheral blood progenitor cells (PBPC), can be expanded in ex vivo culture and can be infused in tandem with unmanipulated PBPC with little or no toxicity. In this study, four patients (two non-Hodgkin's lymphoma (NHL), two multi...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 1997-06, Vol.19 (11), p.1095-1101
Hauptverfasser: HOLYOAKE, T. L, ALCORN, M. J, RICHMOND, L, FARRELL, E, PEARSON, C, GREEN, R, DUNLOP, D. J, FITZSIMONS, E, PRAGNELL, I. B, FRANKLIN, I. M
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container_end_page 1101
container_issue 11
container_start_page 1095
container_title Bone marrow transplantation (Basingstoke)
container_volume 19
creator HOLYOAKE, T. L
ALCORN, M. J
RICHMOND, L
FARRELL, E
PEARSON, C
GREEN, R
DUNLOP, D. J
FITZSIMONS, E
PRAGNELL, I. B
FRANKLIN, I. M
description We have previously demonstrated that CD34+ cells, selected from peripheral blood progenitor cells (PBPC), can be expanded in ex vivo culture and can be infused in tandem with unmanipulated PBPC with little or no toxicity. In this study, four patients (two non-Hodgkin's lymphoma (NHL), two multiple myeloma (MM)) received myeloablative conditioning prior to stem cell rescue using ex vivo expanded cells alone. The two patients with NHL received cyclophosphamide and total body irradiation (CY/TBI) and the two patients with MM, busulphan and melphalan (Bu/M). One case received an inadequate CFU-GM dose, despite expansion, and in one case the expanded cells were contaminated. No definitive conclusions may therefore be drawn concerning engraftment in these two cases. However, the other two cases received high doses of committed progenitors. Following infusion of the expanded material, all four patients failed to show sustained neutrophil engraftment and none showed evidence of platelet engraftment. Back-up, unmanipulated PBPC were therefore infused on days 14, 34, 32 and 28 and subsequently all four cases achieved satisfactory engraftment of both neutrophils and platelets. In conclusion, we feel that, CD34+ cells, expanded ex vivo using the conditions described in this report, may not provide durable engraftment following fully myeloablative conditioning.
doi_str_mv 10.1038/sj.bmt.1700799
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L ; ALCORN, M. J ; RICHMOND, L ; FARRELL, E ; PEARSON, C ; GREEN, R ; DUNLOP, D. J ; FITZSIMONS, E ; PRAGNELL, I. B ; FRANKLIN, I. M</creator><creatorcontrib>HOLYOAKE, T. L ; ALCORN, M. J ; RICHMOND, L ; FARRELL, E ; PEARSON, C ; GREEN, R ; DUNLOP, D. J ; FITZSIMONS, E ; PRAGNELL, I. B ; FRANKLIN, I. M</creatorcontrib><description>We have previously demonstrated that CD34+ cells, selected from peripheral blood progenitor cells (PBPC), can be expanded in ex vivo culture and can be infused in tandem with unmanipulated PBPC with little or no toxicity. In this study, four patients (two non-Hodgkin's lymphoma (NHL), two multiple myeloma (MM)) received myeloablative conditioning prior to stem cell rescue using ex vivo expanded cells alone. The two patients with NHL received cyclophosphamide and total body irradiation (CY/TBI) and the two patients with MM, busulphan and melphalan (Bu/M). One case received an inadequate CFU-GM dose, despite expansion, and in one case the expanded cells were contaminated. No definitive conclusions may therefore be drawn concerning engraftment in these two cases. However, the other two cases received high doses of committed progenitors. Following infusion of the expanded material, all four patients failed to show sustained neutrophil engraftment and none showed evidence of platelet engraftment. Back-up, unmanipulated PBPC were therefore infused on days 14, 34, 32 and 28 and subsequently all four cases achieved satisfactory engraftment of both neutrophils and platelets. 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Graft versus host reaction ; Busulfan ; CD34 antigen ; Cell culture ; Chemoradiotherapy ; Chemotherapy ; Conditioning ; Cyclophosphamide ; Granulocyte Colony-Stimulating Factor - pharmacology ; Hematopoietic Stem Cell Transplantation ; Hemopoiesis ; Humans ; Irradiation ; Leukocytes (neutrophilic) ; Lymphoma ; Lymphoma, Non-Hodgkin - therapy ; Medical sciences ; Melphalan ; Middle Aged ; Multiple myeloma ; Multiple Myeloma - therapy ; Non-Hodgkin's lymphoma ; Peripheral blood ; Platelets ; Progenitor cells ; Radiation ; Radiation therapy ; Stem cell transplantation ; Stem cells ; Toxicity ; Transfusions. Complications. Transfusion reactions. 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L</creatorcontrib><creatorcontrib>ALCORN, M. J</creatorcontrib><creatorcontrib>RICHMOND, L</creatorcontrib><creatorcontrib>FARRELL, E</creatorcontrib><creatorcontrib>PEARSON, C</creatorcontrib><creatorcontrib>GREEN, R</creatorcontrib><creatorcontrib>DUNLOP, D. J</creatorcontrib><creatorcontrib>FITZSIMONS, E</creatorcontrib><creatorcontrib>PRAGNELL, I. B</creatorcontrib><creatorcontrib>FRANKLIN, I. M</creatorcontrib><title>CD34 positive PBPC expanded ex vivo may not provide durable engraftment following myeloablative chemoradiotherapy regimens</title><title>Bone marrow transplantation (Basingstoke)</title><addtitle>Bone Marrow Transplant</addtitle><description>We have previously demonstrated that CD34+ cells, selected from peripheral blood progenitor cells (PBPC), can be expanded in ex vivo culture and can be infused in tandem with unmanipulated PBPC with little or no toxicity. 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In conclusion, we feel that, CD34+ cells, expanded ex vivo using the conditions described in this report, may not provide durable engraftment following fully myeloablative conditioning.</description><subject>Adult</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Antigens, CD34 - analysis</subject><subject>Biological and medical sciences</subject><subject>Bone marrow</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Busulfan</subject><subject>CD34 antigen</subject><subject>Cell culture</subject><subject>Chemoradiotherapy</subject><subject>Chemotherapy</subject><subject>Conditioning</subject><subject>Cyclophosphamide</subject><subject>Granulocyte Colony-Stimulating Factor - pharmacology</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Hemopoiesis</subject><subject>Humans</subject><subject>Irradiation</subject><subject>Leukocytes (neutrophilic)</subject><subject>Lymphoma</subject><subject>Lymphoma, Non-Hodgkin - therapy</subject><subject>Medical sciences</subject><subject>Melphalan</subject><subject>Middle Aged</subject><subject>Multiple myeloma</subject><subject>Multiple Myeloma - therapy</subject><subject>Non-Hodgkin's lymphoma</subject><subject>Peripheral blood</subject><subject>Platelets</subject><subject>Progenitor cells</subject><subject>Radiation</subject><subject>Radiation therapy</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Toxicity</subject><subject>Transfusions. 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Graft versus host reaction</topic><topic>Busulfan</topic><topic>CD34 antigen</topic><topic>Cell culture</topic><topic>Chemoradiotherapy</topic><topic>Chemotherapy</topic><topic>Conditioning</topic><topic>Cyclophosphamide</topic><topic>Granulocyte Colony-Stimulating Factor - pharmacology</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Hemopoiesis</topic><topic>Humans</topic><topic>Irradiation</topic><topic>Leukocytes (neutrophilic)</topic><topic>Lymphoma</topic><topic>Lymphoma, Non-Hodgkin - therapy</topic><topic>Medical sciences</topic><topic>Melphalan</topic><topic>Middle Aged</topic><topic>Multiple myeloma</topic><topic>Multiple Myeloma - therapy</topic><topic>Non-Hodgkin's lymphoma</topic><topic>Peripheral blood</topic><topic>Platelets</topic><topic>Progenitor cells</topic><topic>Radiation</topic><topic>Radiation therapy</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><topic>Toxicity</topic><topic>Transfusions. Complications. 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L</au><au>ALCORN, M. J</au><au>RICHMOND, L</au><au>FARRELL, E</au><au>PEARSON, C</au><au>GREEN, R</au><au>DUNLOP, D. J</au><au>FITZSIMONS, E</au><au>PRAGNELL, I. B</au><au>FRANKLIN, I. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD34 positive PBPC expanded ex vivo may not provide durable engraftment following myeloablative chemoradiotherapy regimens</atitle><jtitle>Bone marrow transplantation (Basingstoke)</jtitle><addtitle>Bone Marrow Transplant</addtitle><date>1997-06-01</date><risdate>1997</risdate><volume>19</volume><issue>11</issue><spage>1095</spage><epage>1101</epage><pages>1095-1101</pages><issn>0268-3369</issn><eissn>1476-5365</eissn><coden>BMTRE9</coden><abstract>We have previously demonstrated that CD34+ cells, selected from peripheral blood progenitor cells (PBPC), can be expanded in ex vivo culture and can be infused in tandem with unmanipulated PBPC with little or no toxicity. In this study, four patients (two non-Hodgkin's lymphoma (NHL), two multiple myeloma (MM)) received myeloablative conditioning prior to stem cell rescue using ex vivo expanded cells alone. The two patients with NHL received cyclophosphamide and total body irradiation (CY/TBI) and the two patients with MM, busulphan and melphalan (Bu/M). One case received an inadequate CFU-GM dose, despite expansion, and in one case the expanded cells were contaminated. No definitive conclusions may therefore be drawn concerning engraftment in these two cases. However, the other two cases received high doses of committed progenitors. Following infusion of the expanded material, all four patients failed to show sustained neutrophil engraftment and none showed evidence of platelet engraftment. Back-up, unmanipulated PBPC were therefore infused on days 14, 34, 32 and 28 and subsequently all four cases achieved satisfactory engraftment of both neutrophils and platelets. In conclusion, we feel that, CD34+ cells, expanded ex vivo using the conditions described in this report, may not provide durable engraftment following fully myeloablative conditioning.</abstract><cop>Basingstoke</cop><pub>Nature Publishing Group</pub><pmid>9193752</pmid><doi>10.1038/sj.bmt.1700799</doi><tpages>7</tpages></addata></record>
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subjects Adult
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Antigens, CD34 - analysis
Biological and medical sciences
Bone marrow
Bone marrow, stem cells transplantation. Graft versus host reaction
Busulfan
CD34 antigen
Cell culture
Chemoradiotherapy
Chemotherapy
Conditioning
Cyclophosphamide
Granulocyte Colony-Stimulating Factor - pharmacology
Hematopoietic Stem Cell Transplantation
Hemopoiesis
Humans
Irradiation
Leukocytes (neutrophilic)
Lymphoma
Lymphoma, Non-Hodgkin - therapy
Medical sciences
Melphalan
Middle Aged
Multiple myeloma
Multiple Myeloma - therapy
Non-Hodgkin's lymphoma
Peripheral blood
Platelets
Progenitor cells
Radiation
Radiation therapy
Stem cell transplantation
Stem cells
Toxicity
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Transplantation Conditioning
title CD34 positive PBPC expanded ex vivo may not provide durable engraftment following myeloablative chemoradiotherapy regimens
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