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Immunomagnetic selection of CD34+ cells: factors influencing component purity and yield
BACKGROUND: In immunomagnetic selection of CD34+ cells from HPC transplants, not all factors that affect yield and purity of CD34+ cells are known. METHODS: Forty‐three consecutive procedures of immunomagnetic selection of CD34+ cells from peripheral blood HPCs and bone marrow harvests (autologous h...
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Published in: | Transfusion (Philadelphia, Pa.) Pa.), 2000-05, Vol.40 (5), p.507-512 |
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creator | Hildebrandt, M. Serke, S. Meyer, O. Ebell, W. Salama, A. |
description | BACKGROUND: In immunomagnetic selection of CD34+ cells from HPC transplants, not all factors that affect yield and purity of CD34+ cells are known.
METHODS: Forty‐three consecutive procedures of immunomagnetic selection of CD34+ cells from peripheral blood HPCs and bone marrow harvests (autologous harvests, n = 27; allogeneic harvests; n=16) were performed by use of a cell selection system (Isolex 300i, Baxter Immunotherapy). The composition of the starting component and the subsets of CD34+ cells were analyzed for correlation with the yield and purity of the final component.
RESULTS: The mean purity of the final components was 84.3 percent (range, 27‐99%), and the mean yield was 51.4 percent (range, 9.4‐80.4%). Partial regression analysis showed that, among the factors correlating with purity and/or yield, the RBC volume in the starting fraction had the highest predictive impact on the purity and yield of CD34+ cells, even after the exclusion of procedures using bone marrow harvests as an HPC source (beta coefficient, –0.704; p = 0.001).
CONCLUSION: The use of the Isolex 300i system allows efficient recovery of CD34+ cells in routine selection procedures. The volume of RBCs in the starting component should be minimized to ensure a high yield and purity of the final component. |
doi_str_mv | 10.1046/j.1537-2995.2000.40050507.x |
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METHODS: Forty‐three consecutive procedures of immunomagnetic selection of CD34+ cells from peripheral blood HPCs and bone marrow harvests (autologous harvests, n = 27; allogeneic harvests; n=16) were performed by use of a cell selection system (Isolex 300i, Baxter Immunotherapy). The composition of the starting component and the subsets of CD34+ cells were analyzed for correlation with the yield and purity of the final component.
RESULTS: The mean purity of the final components was 84.3 percent (range, 27‐99%), and the mean yield was 51.4 percent (range, 9.4‐80.4%). Partial regression analysis showed that, among the factors correlating with purity and/or yield, the RBC volume in the starting fraction had the highest predictive impact on the purity and yield of CD34+ cells, even after the exclusion of procedures using bone marrow harvests as an HPC source (beta coefficient, –0.704; p = 0.001).
CONCLUSION: The use of the Isolex 300i system allows efficient recovery of CD34+ cells in routine selection procedures. The volume of RBCs in the starting component should be minimized to ensure a high yield and purity of the final component.</description><identifier>ISSN: 0041-1132</identifier><identifier>EISSN: 1537-2995</identifier><identifier>DOI: 10.1046/j.1537-2995.2000.40050507.x</identifier><identifier>PMID: 10827251</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Inc</publisher><subject>ALL = acute lymphatic leukemia ; Antigens, CD34 - blood ; Hematocrit ; Humans ; Immunomagnetic Separation - methods ; Linear Models ; NC(s) = nucleated cell(s) ; Neuroblastoma - blood ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - blood ; Sarcoma, Ewing - blood</subject><ispartof>Transfusion (Philadelphia, Pa.), 2000-05, Vol.40 (5), p.507-512</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4697-2679676e7bc7f6891a33f16c321fb6973959d915474ba8d62f167634d65f09f43</citedby><cites>FETCH-LOGICAL-c4697-2679676e7bc7f6891a33f16c321fb6973959d915474ba8d62f167634d65f09f43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10827251$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hildebrandt, M.</creatorcontrib><creatorcontrib>Serke, S.</creatorcontrib><creatorcontrib>Meyer, O.</creatorcontrib><creatorcontrib>Ebell, W.</creatorcontrib><creatorcontrib>Salama, A.</creatorcontrib><title>Immunomagnetic selection of CD34+ cells: factors influencing component purity and yield</title><title>Transfusion (Philadelphia, Pa.)</title><addtitle>Transfusion</addtitle><description>BACKGROUND: In immunomagnetic selection of CD34+ cells from HPC transplants, not all factors that affect yield and purity of CD34+ cells are known.
METHODS: Forty‐three consecutive procedures of immunomagnetic selection of CD34+ cells from peripheral blood HPCs and bone marrow harvests (autologous harvests, n = 27; allogeneic harvests; n=16) were performed by use of a cell selection system (Isolex 300i, Baxter Immunotherapy). The composition of the starting component and the subsets of CD34+ cells were analyzed for correlation with the yield and purity of the final component.
RESULTS: The mean purity of the final components was 84.3 percent (range, 27‐99%), and the mean yield was 51.4 percent (range, 9.4‐80.4%). Partial regression analysis showed that, among the factors correlating with purity and/or yield, the RBC volume in the starting fraction had the highest predictive impact on the purity and yield of CD34+ cells, even after the exclusion of procedures using bone marrow harvests as an HPC source (beta coefficient, –0.704; p = 0.001).
CONCLUSION: The use of the Isolex 300i system allows efficient recovery of CD34+ cells in routine selection procedures. The volume of RBCs in the starting component should be minimized to ensure a high yield and purity of the final component.</description><subject>ALL = acute lymphatic leukemia</subject><subject>Antigens, CD34 - blood</subject><subject>Hematocrit</subject><subject>Humans</subject><subject>Immunomagnetic Separation - methods</subject><subject>Linear Models</subject><subject>NC(s) = nucleated cell(s)</subject><subject>Neuroblastoma - blood</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - blood</subject><subject>Sarcoma, Ewing - blood</subject><issn>0041-1132</issn><issn>1537-2995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqVkE1r3DAQhkVpaTbb_oUiKPRS7GosWVq1p7DbpIH0g5CS3oRWloK2trS1bLr77yPjJPRa5iCGeefR8CD0FkgJhPEPuxJqKopKyrqsCCElI6TOJcrDM7R4mj1HC0IYFAC0OkGnKe1ytpIEXqITIKtKVDUs0O1l140hdvou2MEbnGxrzeBjwNHh9Yay99jYtk0fsdNmiH3CPrh2tMH4cIdN7PYx2DDg_dj74Yh1aPDR27Z5hV443Sb7-uFdop_nn2_WX4qr7xeX67OrwjAu86FcSC64FVsjHF9J0JQ64IZW4LY5QGUtGwk1E2yrVw2v8lBwyhpeOyIdo0v0bubu-_hntGlQnU_TxTrYOCYlABiIDFqiT3PQ9DGl3jq1732n-6MCoiavaqcmd2pypyav6tGrOuTtNw_fjNvONv_sziJzYDMH_vrWHv-HrW6uzx-7jClmjE-DPTxhdP9bcUFFrW6_XaivP36tNtcbodb0Hlmfljw</recordid><startdate>200005</startdate><enddate>200005</enddate><creator>Hildebrandt, M.</creator><creator>Serke, S.</creator><creator>Meyer, O.</creator><creator>Ebell, W.</creator><creator>Salama, A.</creator><general>Blackwell Science Inc</general><scope>BSCLL</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>7X8</scope></search><sort><creationdate>200005</creationdate><title>Immunomagnetic selection of CD34+ cells: factors influencing component purity and yield</title><author>Hildebrandt, M. ; Serke, S. ; Meyer, O. ; Ebell, W. ; Salama, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4697-2679676e7bc7f6891a33f16c321fb6973959d915474ba8d62f167634d65f09f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>ALL = acute lymphatic leukemia</topic><topic>Antigens, CD34 - blood</topic><topic>Hematocrit</topic><topic>Humans</topic><topic>Immunomagnetic Separation - methods</topic><topic>Linear Models</topic><topic>NC(s) = nucleated cell(s)</topic><topic>Neuroblastoma - blood</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - blood</topic><topic>Sarcoma, Ewing - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hildebrandt, M.</creatorcontrib><creatorcontrib>Serke, S.</creatorcontrib><creatorcontrib>Meyer, O.</creatorcontrib><creatorcontrib>Ebell, W.</creatorcontrib><creatorcontrib>Salama, A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transfusion (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hildebrandt, M.</au><au>Serke, S.</au><au>Meyer, O.</au><au>Ebell, W.</au><au>Salama, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunomagnetic selection of CD34+ cells: factors influencing component purity and yield</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><addtitle>Transfusion</addtitle><date>2000-05</date><risdate>2000</risdate><volume>40</volume><issue>5</issue><spage>507</spage><epage>512</epage><pages>507-512</pages><issn>0041-1132</issn><eissn>1537-2995</eissn><abstract>BACKGROUND: In immunomagnetic selection of CD34+ cells from HPC transplants, not all factors that affect yield and purity of CD34+ cells are known.
METHODS: Forty‐three consecutive procedures of immunomagnetic selection of CD34+ cells from peripheral blood HPCs and bone marrow harvests (autologous harvests, n = 27; allogeneic harvests; n=16) were performed by use of a cell selection system (Isolex 300i, Baxter Immunotherapy). The composition of the starting component and the subsets of CD34+ cells were analyzed for correlation with the yield and purity of the final component.
RESULTS: The mean purity of the final components was 84.3 percent (range, 27‐99%), and the mean yield was 51.4 percent (range, 9.4‐80.4%). Partial regression analysis showed that, among the factors correlating with purity and/or yield, the RBC volume in the starting fraction had the highest predictive impact on the purity and yield of CD34+ cells, even after the exclusion of procedures using bone marrow harvests as an HPC source (beta coefficient, –0.704; p = 0.001).
CONCLUSION: The use of the Isolex 300i system allows efficient recovery of CD34+ cells in routine selection procedures. The volume of RBCs in the starting component should be minimized to ensure a high yield and purity of the final component.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Inc</pub><pmid>10827251</pmid><doi>10.1046/j.1537-2995.2000.40050507.x</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ALL = acute lymphatic leukemia Antigens, CD34 - blood Hematocrit Humans Immunomagnetic Separation - methods Linear Models NC(s) = nucleated cell(s) Neuroblastoma - blood Precursor Cell Lymphoblastic Leukemia-Lymphoma - blood Sarcoma, Ewing - blood |
title | Immunomagnetic selection of CD34+ cells: factors influencing component purity and yield |
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