Transduction of Umbilical Cord Blood CD34+ NOD/SCID-Repopulating Cells by Simian Foamy Virus Type 1 (SFV-1) Vector
Foamy viruses are nonpathogenic retroviruses that offer unique opportunities for gene transfer into various cell types including hematopoietic stem cells. We used a simian foamy virus type 1 vector (SFV-1) containing a LacZ reporter gene with a titer of 1–5 × 10 6 viral particles/ml that was free of...
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Veröffentlicht in: | Virology (New York, N.Y.) N.Y.), 2002-10, Vol.302 (2), p.229-235 |
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creator | Zucali, James R. Ciccarone, Tina Kelley, Vicky Park, Jeonghae Johnson, Calvin M. Mergia, Ayalew |
description | Foamy viruses are nonpathogenic retroviruses that offer unique opportunities for gene transfer into various cell types including hematopoietic stem cells. We used a simian foamy virus type 1 vector (SFV-1) containing a
LacZ reporter gene with a titer of 1–5 × 10
6 viral particles/ml that was free of replication-competent retrovirus to transduce human umbilical cord blood CD34+ cells. Transduced CD34+ cord blood cells were transplanted into NOD/SCID mice and plated in serum-free methylcellulose culture to determine the transduction efficiency of human hematopoietic progenitor cells. A transduction efficiency of about 20% was obtained. At 6–10 weeks posttransplantation, human hematopoietic cell engraftment and marking were determined. Marrow from transplanted mice demonstrated human cell engraftment by the presence of human (CD45+) cells containing both CD19+ lymphoid and CD33+ myeloid cells. Serial sampling of NOD/SCID bone marrow revealed the presence of 6.7–14.0% CD45+ cells at 6 weeks posttransplant as compared to 3.6–27.2% CD45+ cells at 9–10 weeks posttransplant. Human progenitors examined from NOD/SCID bone marrow cells 9 weeks posttransplant revealed from 7.4 to 25.9% of the colonies exhibiting X-gal staining. Our study demonstrates the ability of a simian foamy virus vector to transduce the SCID-repopulating cell and offers a promising new gene delivery system for use in hematopoietic stem cell gene therapy. |
doi_str_mv | 10.1006/viro.2002.1604 |
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LacZ reporter gene with a titer of 1–5 × 10
6 viral particles/ml that was free of replication-competent retrovirus to transduce human umbilical cord blood CD34+ cells. Transduced CD34+ cord blood cells were transplanted into NOD/SCID mice and plated in serum-free methylcellulose culture to determine the transduction efficiency of human hematopoietic progenitor cells. A transduction efficiency of about 20% was obtained. At 6–10 weeks posttransplantation, human hematopoietic cell engraftment and marking were determined. Marrow from transplanted mice demonstrated human cell engraftment by the presence of human (CD45+) cells containing both CD19+ lymphoid and CD33+ myeloid cells. Serial sampling of NOD/SCID bone marrow revealed the presence of 6.7–14.0% CD45+ cells at 6 weeks posttransplant as compared to 3.6–27.2% CD45+ cells at 9–10 weeks posttransplant. Human progenitors examined from NOD/SCID bone marrow cells 9 weeks posttransplant revealed from 7.4 to 25.9% of the colonies exhibiting X-gal staining. Our study demonstrates the ability of a simian foamy virus vector to transduce the SCID-repopulating cell and offers a promising new gene delivery system for use in hematopoietic stem cell gene therapy.</description><identifier>ISSN: 0042-6822</identifier><identifier>EISSN: 1096-0341</identifier><identifier>DOI: 10.1006/viro.2002.1604</identifier><identifier>PMID: 12441067</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Antigens, CD34 - blood ; CD34+ cells ; Cells, Cultured ; Fetal Blood - cytology ; foamy virus ; Gene Transfer Techniques ; Genetic Vectors ; Hematopoietic Stem Cell Transplantation ; Hematopoietic Stem Cells - cytology ; Humans ; Lac Operon - genetics ; Mice ; Mice, Inbred NOD ; Mice, SCID ; NOD/SCID ; Reverse Transcriptase Polymerase Chain Reaction ; Spumavirus - genetics ; Transduction, Genetic</subject><ispartof>Virology (New York, N.Y.), 2002-10, Vol.302 (2), p.229-235</ispartof><rights>2002 Elsevier Science (USA)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-b42411d13c9e510a2d4813822fe7c4b45d961cddb19f7ff63c95d0c577cae0a63</citedby><cites>FETCH-LOGICAL-c411t-b42411d13c9e510a2d4813822fe7c4b45d961cddb19f7ff63c95d0c577cae0a63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0042682202916041$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12441067$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zucali, James R.</creatorcontrib><creatorcontrib>Ciccarone, Tina</creatorcontrib><creatorcontrib>Kelley, Vicky</creatorcontrib><creatorcontrib>Park, Jeonghae</creatorcontrib><creatorcontrib>Johnson, Calvin M.</creatorcontrib><creatorcontrib>Mergia, Ayalew</creatorcontrib><title>Transduction of Umbilical Cord Blood CD34+ NOD/SCID-Repopulating Cells by Simian Foamy Virus Type 1 (SFV-1) Vector</title><title>Virology (New York, N.Y.)</title><addtitle>Virology</addtitle><description>Foamy viruses are nonpathogenic retroviruses that offer unique opportunities for gene transfer into various cell types including hematopoietic stem cells. We used a simian foamy virus type 1 vector (SFV-1) containing a
LacZ reporter gene with a titer of 1–5 × 10
6 viral particles/ml that was free of replication-competent retrovirus to transduce human umbilical cord blood CD34+ cells. Transduced CD34+ cord blood cells were transplanted into NOD/SCID mice and plated in serum-free methylcellulose culture to determine the transduction efficiency of human hematopoietic progenitor cells. A transduction efficiency of about 20% was obtained. At 6–10 weeks posttransplantation, human hematopoietic cell engraftment and marking were determined. Marrow from transplanted mice demonstrated human cell engraftment by the presence of human (CD45+) cells containing both CD19+ lymphoid and CD33+ myeloid cells. Serial sampling of NOD/SCID bone marrow revealed the presence of 6.7–14.0% CD45+ cells at 6 weeks posttransplant as compared to 3.6–27.2% CD45+ cells at 9–10 weeks posttransplant. Human progenitors examined from NOD/SCID bone marrow cells 9 weeks posttransplant revealed from 7.4 to 25.9% of the colonies exhibiting X-gal staining. Our study demonstrates the ability of a simian foamy virus vector to transduce the SCID-repopulating cell and offers a promising new gene delivery system for use in hematopoietic stem cell gene therapy.</description><subject>Animals</subject><subject>Antigens, CD34 - blood</subject><subject>CD34+ cells</subject><subject>Cells, Cultured</subject><subject>Fetal Blood - cytology</subject><subject>foamy virus</subject><subject>Gene Transfer Techniques</subject><subject>Genetic Vectors</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Hematopoietic Stem Cells - cytology</subject><subject>Humans</subject><subject>Lac Operon - genetics</subject><subject>Mice</subject><subject>Mice, Inbred NOD</subject><subject>Mice, SCID</subject><subject>NOD/SCID</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Spumavirus - genetics</subject><subject>Transduction, Genetic</subject><issn>0042-6822</issn><issn>1096-0341</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcGLEzEUxoMobl29epScRJHpvpfJJO1Rp1YXFhdst9eQSTISmZnMJjML_e9NacGTePp48Hsf730fIW8Rlgggbp58DEsGwJYogD8jC4S1KKDk-JwsADgrxIqxK_Iqpd-QZynhJblCxjmCkAsS91EPyc5m8mGgoaUPfeM7b3RH6xAt_dKFYGm9Kfkn-uN-c7OrbzfFTzeGce705IdftHZdl2hzpDvfez3QbdD9kR58nBPdH0dHkX7YbQ8FfqQHZ6YQX5MXre6Se3PRa_Kw_bqvvxd3999u6893heGIU9FwltViadauQtDM8hWW-ZnWScMbXtm1QGNtg-tWtq3IXGXBVFIa7UCL8pq8P_uOMTzOLk2q98nka_XgwpyUZBIkVv8HcSVKVknI4PIMmhhSiq5VY_S9jkeFoE51qFMd6lSHOtWRF95dnOemd_Yvfsk_A6sz4HIQT95FlYx3g3HWxxyWssH_y_sPmQ6Wkw</recordid><startdate>20021025</startdate><enddate>20021025</enddate><creator>Zucali, James R.</creator><creator>Ciccarone, Tina</creator><creator>Kelley, Vicky</creator><creator>Park, Jeonghae</creator><creator>Johnson, Calvin M.</creator><creator>Mergia, Ayalew</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20021025</creationdate><title>Transduction of Umbilical Cord Blood CD34+ NOD/SCID-Repopulating Cells by Simian Foamy Virus Type 1 (SFV-1) Vector</title><author>Zucali, James R. ; Ciccarone, Tina ; Kelley, Vicky ; Park, Jeonghae ; Johnson, Calvin M. ; Mergia, Ayalew</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-b42411d13c9e510a2d4813822fe7c4b45d961cddb19f7ff63c95d0c577cae0a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Antigens, CD34 - blood</topic><topic>CD34+ cells</topic><topic>Cells, Cultured</topic><topic>Fetal Blood - cytology</topic><topic>foamy virus</topic><topic>Gene Transfer Techniques</topic><topic>Genetic Vectors</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Hematopoietic Stem Cells - cytology</topic><topic>Humans</topic><topic>Lac Operon - genetics</topic><topic>Mice</topic><topic>Mice, Inbred NOD</topic><topic>Mice, SCID</topic><topic>NOD/SCID</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Spumavirus - genetics</topic><topic>Transduction, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zucali, James R.</creatorcontrib><creatorcontrib>Ciccarone, Tina</creatorcontrib><creatorcontrib>Kelley, Vicky</creatorcontrib><creatorcontrib>Park, Jeonghae</creatorcontrib><creatorcontrib>Johnson, Calvin M.</creatorcontrib><creatorcontrib>Mergia, Ayalew</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Virology (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zucali, James R.</au><au>Ciccarone, Tina</au><au>Kelley, Vicky</au><au>Park, Jeonghae</au><au>Johnson, Calvin M.</au><au>Mergia, Ayalew</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transduction of Umbilical Cord Blood CD34+ NOD/SCID-Repopulating Cells by Simian Foamy Virus Type 1 (SFV-1) Vector</atitle><jtitle>Virology (New York, N.Y.)</jtitle><addtitle>Virology</addtitle><date>2002-10-25</date><risdate>2002</risdate><volume>302</volume><issue>2</issue><spage>229</spage><epage>235</epage><pages>229-235</pages><issn>0042-6822</issn><eissn>1096-0341</eissn><abstract>Foamy viruses are nonpathogenic retroviruses that offer unique opportunities for gene transfer into various cell types including hematopoietic stem cells. We used a simian foamy virus type 1 vector (SFV-1) containing a
LacZ reporter gene with a titer of 1–5 × 10
6 viral particles/ml that was free of replication-competent retrovirus to transduce human umbilical cord blood CD34+ cells. Transduced CD34+ cord blood cells were transplanted into NOD/SCID mice and plated in serum-free methylcellulose culture to determine the transduction efficiency of human hematopoietic progenitor cells. A transduction efficiency of about 20% was obtained. At 6–10 weeks posttransplantation, human hematopoietic cell engraftment and marking were determined. Marrow from transplanted mice demonstrated human cell engraftment by the presence of human (CD45+) cells containing both CD19+ lymphoid and CD33+ myeloid cells. Serial sampling of NOD/SCID bone marrow revealed the presence of 6.7–14.0% CD45+ cells at 6 weeks posttransplant as compared to 3.6–27.2% CD45+ cells at 9–10 weeks posttransplant. Human progenitors examined from NOD/SCID bone marrow cells 9 weeks posttransplant revealed from 7.4 to 25.9% of the colonies exhibiting X-gal staining. Our study demonstrates the ability of a simian foamy virus vector to transduce the SCID-repopulating cell and offers a promising new gene delivery system for use in hematopoietic stem cell gene therapy.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>12441067</pmid><doi>10.1006/viro.2002.1604</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigens, CD34 - blood CD34+ cells Cells, Cultured Fetal Blood - cytology foamy virus Gene Transfer Techniques Genetic Vectors Hematopoietic Stem Cell Transplantation Hematopoietic Stem Cells - cytology Humans Lac Operon - genetics Mice Mice, Inbred NOD Mice, SCID NOD/SCID Reverse Transcriptase Polymerase Chain Reaction Spumavirus - genetics Transduction, Genetic |
title | Transduction of Umbilical Cord Blood CD34+ NOD/SCID-Repopulating Cells by Simian Foamy Virus Type 1 (SFV-1) Vector |
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