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 |
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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. 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><identifier>ISSN: 0268-3369</identifier><identifier>EISSN: 1476-5365</identifier><identifier>DOI: 10.1038/sj.bmt.1700799</identifier><identifier>PMID: 9193752</identifier><identifier>CODEN: BMTRE9</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing Group</publisher><subject>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</subject><ispartof>Bone marrow transplantation (Basingstoke), 1997-06, Vol.19 (11), p.1095-1101</ispartof><rights>1997 INIST-CNRS</rights><rights>Macmillan Publishers Limited 1997.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-31952022def1ec91344852cb76f61932ddc2d07433e1cf99a42f71c429933dec3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2679590$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9193752$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HOLYOAKE, T. 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. 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.</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. Complications. Transfusion reactions. Cell and gene therapy</subject><subject>Transplantation Conditioning</subject><issn>0268-3369</issn><issn>1476-5365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kM1PGzEQxS3UKg0fV26VLLXXDf5aOz62KbRISM0BzivHHgdHu-utvQmEvx5TVpxmpPfmzcwPoUtKFpTw5VXeLTbduKCKEKX1CZpToWRVc1l_QnPC5LLiXOov6DTnHSFUCFLP0ExTzVXN5uhl9YsLPMQcxnAAvP65XmF4HkzvwJUGH8Ih4s4ccR9HPKR4CA6w2yezaQFDv03Gjx30I_axbeNT6Le4O0Ibi27-J9pH6GIyLsTxEZIZjjjBNpSRfI4-e9NmuJjqGXq4ub5f_anu_v6-Xf24qyxXcqw41TUjjDnwFKymXIhlzexGSS_LF8w5yxxRgnOg1mttBPOKWsG05tyB5Wfo23tuOf_fHvLY7OI-9WVlw6RglFJJ6uJavLtsijkn8M2QQmfSsaGkeSPd5F1TSDcT6TLwdYrdbzpwH_YJbdG_T7rJ1rQ-md6G_GFjUulaE_4KOgmIWQ</recordid><startdate>19970601</startdate><enddate>19970601</enddate><creator>HOLYOAKE, T. L</creator><creator>ALCORN, M. J</creator><creator>RICHMOND, L</creator><creator>FARRELL, E</creator><creator>PEARSON, C</creator><creator>GREEN, R</creator><creator>DUNLOP, D. J</creator><creator>FITZSIMONS, E</creator><creator>PRAGNELL, I. B</creator><creator>FRANKLIN, I. M</creator><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QP</scope><scope>7T5</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>19970601</creationdate><title>CD34 positive PBPC expanded ex vivo may not provide durable engraftment following myeloablative chemoradiotherapy regimens</title><author>HOLYOAKE, T. L ; ALCORN, M. J ; RICHMOND, L ; FARRELL, E ; PEARSON, C ; GREEN, R ; DUNLOP, D. J ; FITZSIMONS, E ; PRAGNELL, I. B ; FRANKLIN, I. 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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. Transfusion reactions. Cell and gene therapy</topic><topic>Transplantation Conditioning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HOLYOAKE, T. 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. 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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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