Angiogenesis Facilitated by Autologous Whole Bone Marrow Stem Cell Transplantation for Buerger's Disease
We hypothesized that angiogenesis can be triggered by autologous whole bone marrow stem cell transplantation. Twenty‐seven patients (34 lower limbs) with Buerger's disease, who were not candidates for surgical revascularization or radiologic intervention, were enrolled in this study. Six sites...
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creator | Kim, Dong‐Ik Kim, Mi‐Jung Joh, Jin‐Hyun Shin, Sung‐Wook Do, Young‐Soo Moon, Ji‐Young Kim, Na‐Ri Lim, Joung‐Eun Kim, Ae‐Kyeong Eo, Hyun‐Seon Kim, Byung‐Soo Cho, Seung‐Woo Yang, Seung‐Hye Park, Chan‐Jeoung Shim, Jong‐Sup |
description | We hypothesized that angiogenesis can be triggered by autologous whole bone marrow stem cell transplantation. Twenty‐seven patients (34 lower limbs) with Buerger's disease, who were not candidates for surgical revascularization or radiologic intervention, were enrolled in this study. Six sites of the tibia bone were fenestrated using a 2.5‐mm‐diameter screw under fluoroscopic guidance. Clinical status and outcome were determined using the “Recommended Standards for Reports.” To mobilize endothelial progenitor cells (EPCs) from bone marrow, recombinant human granulocyte colony‐stimulating factor (r‐HuG‐CSF) was injected subcutaneously as a dose of 75 μg, preoperatively. During the follow‐up period (19.1 ± 3.5 months), one limb showed a markedly improved outcome (+3), and 26 limbs showed a moderately improved outcome (+2). Thirteen limbs among 17 limbs with nonhealing ulcers healed. Postoperative angiograms were obtained for 22 limbs. Two limbs showed marked (+3), five limbs moderate (+2), and nine limbs slight (+1) collateral development. However, six limbs showed no collateral development (0). Peripheral blood and bone marrow samples were analyzed for CD34 and CD133 molecules to enumerate potential EPCs, and EPC numbers were found to be increased in peripheral blood and in bone marrow after r‐HuG‐CSF injection. In conclusion, the transplantation of autologous whole BMCs by fenestration of the tibia bone represents a simple, safe, and effective means of inducing therapeutic angiogenesis in patients with Buerger's disease. |
doi_str_mv | 10.1634/stemcells.2005-0349 |
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Twenty‐seven patients (34 lower limbs) with Buerger's disease, who were not candidates for surgical revascularization or radiologic intervention, were enrolled in this study. Six sites of the tibia bone were fenestrated using a 2.5‐mm‐diameter screw under fluoroscopic guidance. Clinical status and outcome were determined using the “Recommended Standards for Reports.” To mobilize endothelial progenitor cells (EPCs) from bone marrow, recombinant human granulocyte colony‐stimulating factor (r‐HuG‐CSF) was injected subcutaneously as a dose of 75 μg, preoperatively. During the follow‐up period (19.1 ± 3.5 months), one limb showed a markedly improved outcome (+3), and 26 limbs showed a moderately improved outcome (+2). Thirteen limbs among 17 limbs with nonhealing ulcers healed. Postoperative angiograms were obtained for 22 limbs. Two limbs showed marked (+3), five limbs moderate (+2), and nine limbs slight (+1) collateral development. However, six limbs showed no collateral development (0). Peripheral blood and bone marrow samples were analyzed for CD34 and CD133 molecules to enumerate potential EPCs, and EPC numbers were found to be increased in peripheral blood and in bone marrow after r‐HuG‐CSF injection. In conclusion, the transplantation of autologous whole BMCs by fenestration of the tibia bone represents a simple, safe, and effective means of inducing therapeutic angiogenesis in patients with Buerger's disease.</description><identifier>ISSN: 1066-5099</identifier><identifier>EISSN: 1549-4918</identifier><identifier>DOI: 10.1634/stemcells.2005-0349</identifier><identifier>PMID: 16439614</identifier><language>eng</language><publisher>Bristol: John Wiley & Sons, Ltd</publisher><subject>Adult ; Angiogenesis ; Bone marrow ; Bone Marrow Cells ; Female ; Humans ; Male ; Neovascularization, Physiologic ; Stem Cell Transplantation ; Stem cells ; Thromboangiitis Obliterans - therapy ; Transplantation, Autologous ; Treatment Outcome</subject><ispartof>Stem cells (Dayton, Ohio), 2006-05, Vol.24 (5), p.1194-1200</ispartof><rights>Copyright © 2006 AlphaMed Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4524-179c4946c94a5bedc48fd864a8a85176a060272417f6e0c4cabdae32904df8d63</citedby><cites>FETCH-LOGICAL-c4524-179c4946c94a5bedc48fd864a8a85176a060272417f6e0c4cabdae32904df8d63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16439614$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Dong‐Ik</creatorcontrib><creatorcontrib>Kim, Mi‐Jung</creatorcontrib><creatorcontrib>Joh, Jin‐Hyun</creatorcontrib><creatorcontrib>Shin, Sung‐Wook</creatorcontrib><creatorcontrib>Do, Young‐Soo</creatorcontrib><creatorcontrib>Moon, Ji‐Young</creatorcontrib><creatorcontrib>Kim, Na‐Ri</creatorcontrib><creatorcontrib>Lim, Joung‐Eun</creatorcontrib><creatorcontrib>Kim, Ae‐Kyeong</creatorcontrib><creatorcontrib>Eo, Hyun‐Seon</creatorcontrib><creatorcontrib>Kim, Byung‐Soo</creatorcontrib><creatorcontrib>Cho, Seung‐Woo</creatorcontrib><creatorcontrib>Yang, Seung‐Hye</creatorcontrib><creatorcontrib>Park, Chan‐Jeoung</creatorcontrib><creatorcontrib>Shim, Jong‐Sup</creatorcontrib><title>Angiogenesis Facilitated by Autologous Whole Bone Marrow Stem Cell Transplantation for Buerger's Disease</title><title>Stem cells (Dayton, Ohio)</title><addtitle>Stem Cells</addtitle><description>We hypothesized that angiogenesis can be triggered by autologous whole bone marrow stem cell transplantation. Twenty‐seven patients (34 lower limbs) with Buerger's disease, who were not candidates for surgical revascularization or radiologic intervention, were enrolled in this study. Six sites of the tibia bone were fenestrated using a 2.5‐mm‐diameter screw under fluoroscopic guidance. Clinical status and outcome were determined using the “Recommended Standards for Reports.” To mobilize endothelial progenitor cells (EPCs) from bone marrow, recombinant human granulocyte colony‐stimulating factor (r‐HuG‐CSF) was injected subcutaneously as a dose of 75 μg, preoperatively. During the follow‐up period (19.1 ± 3.5 months), one limb showed a markedly improved outcome (+3), and 26 limbs showed a moderately improved outcome (+2). Thirteen limbs among 17 limbs with nonhealing ulcers healed. Postoperative angiograms were obtained for 22 limbs. Two limbs showed marked (+3), five limbs moderate (+2), and nine limbs slight (+1) collateral development. However, six limbs showed no collateral development (0). Peripheral blood and bone marrow samples were analyzed for CD34 and CD133 molecules to enumerate potential EPCs, and EPC numbers were found to be increased in peripheral blood and in bone marrow after r‐HuG‐CSF injection. In conclusion, the transplantation of autologous whole BMCs by fenestration of the tibia bone represents a simple, safe, and effective means of inducing therapeutic angiogenesis in patients with Buerger's disease.</description><subject>Adult</subject><subject>Angiogenesis</subject><subject>Bone marrow</subject><subject>Bone Marrow Cells</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Neovascularization, Physiologic</subject><subject>Stem Cell Transplantation</subject><subject>Stem cells</subject><subject>Thromboangiitis Obliterans - therapy</subject><subject>Transplantation, Autologous</subject><subject>Treatment Outcome</subject><issn>1066-5099</issn><issn>1549-4918</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkTFv2zAQhYkiRe2k_QUFAk7JJJeUThSJTrYbJwUcdIiLjgRNnWwGsuiQEgL_-9KwkY7pdDd87x3uPUK-cjbhooBvscedxbaNk5yxMmMFqA9kzEtQGSguL9LOhMhKptSIXMb4zBiHUspPZMQFFEpwGJPttNs4v8EOo4t0YaxrXW96rOn6QKdD71u_8UOkf7a-RTrzHdJHE4J_pU_pPJ2n-3QVTBf3remS0PmONj7Q2YBhg-E20h8uoon4mXxsTBvxy3lekd-Lu9X8IVv-uv85ny4zC2UOGa-UBQXCKjDlGmsLsqmlACONLHklDBMsr3LgVSOQWbBmXRsscsWgbmQtiityc_LdB_8yYOz1zsVjTKbD9IgWlaoqpdi7IFdK5gXPE1icQBt8jAEbvQ9uZ8JBc6aPTei3JvSxCX1sIqmuz_bDeof1P805-gR8PwGvrsXD_3jqp9XdY3qdKyj-AoLxmrQ</recordid><startdate>200605</startdate><enddate>200605</enddate><creator>Kim, Dong‐Ik</creator><creator>Kim, Mi‐Jung</creator><creator>Joh, Jin‐Hyun</creator><creator>Shin, Sung‐Wook</creator><creator>Do, Young‐Soo</creator><creator>Moon, Ji‐Young</creator><creator>Kim, Na‐Ri</creator><creator>Lim, Joung‐Eun</creator><creator>Kim, Ae‐Kyeong</creator><creator>Eo, Hyun‐Seon</creator><creator>Kim, Byung‐Soo</creator><creator>Cho, Seung‐Woo</creator><creator>Yang, Seung‐Hye</creator><creator>Park, Chan‐Jeoung</creator><creator>Shim, Jong‐Sup</creator><general>John Wiley & Sons, Ltd</general><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>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200605</creationdate><title>Angiogenesis Facilitated by Autologous Whole Bone Marrow Stem Cell Transplantation for Buerger's Disease</title><author>Kim, Dong‐Ik ; Kim, Mi‐Jung ; Joh, Jin‐Hyun ; Shin, Sung‐Wook ; Do, Young‐Soo ; Moon, Ji‐Young ; Kim, Na‐Ri ; Lim, Joung‐Eun ; Kim, Ae‐Kyeong ; Eo, Hyun‐Seon ; Kim, Byung‐Soo ; Cho, Seung‐Woo ; Yang, Seung‐Hye ; Park, Chan‐Jeoung ; Shim, Jong‐Sup</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4524-179c4946c94a5bedc48fd864a8a85176a060272417f6e0c4cabdae32904df8d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Angiogenesis</topic><topic>Bone marrow</topic><topic>Bone Marrow Cells</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Neovascularization, Physiologic</topic><topic>Stem Cell Transplantation</topic><topic>Stem cells</topic><topic>Thromboangiitis Obliterans - therapy</topic><topic>Transplantation, Autologous</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Dong‐Ik</creatorcontrib><creatorcontrib>Kim, Mi‐Jung</creatorcontrib><creatorcontrib>Joh, Jin‐Hyun</creatorcontrib><creatorcontrib>Shin, Sung‐Wook</creatorcontrib><creatorcontrib>Do, Young‐Soo</creatorcontrib><creatorcontrib>Moon, Ji‐Young</creatorcontrib><creatorcontrib>Kim, Na‐Ri</creatorcontrib><creatorcontrib>Lim, Joung‐Eun</creatorcontrib><creatorcontrib>Kim, Ae‐Kyeong</creatorcontrib><creatorcontrib>Eo, Hyun‐Seon</creatorcontrib><creatorcontrib>Kim, Byung‐Soo</creatorcontrib><creatorcontrib>Cho, Seung‐Woo</creatorcontrib><creatorcontrib>Yang, Seung‐Hye</creatorcontrib><creatorcontrib>Park, Chan‐Jeoung</creatorcontrib><creatorcontrib>Shim, Jong‐Sup</creatorcontrib><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>Immunology 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>Stem cells (Dayton, Ohio)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Dong‐Ik</au><au>Kim, Mi‐Jung</au><au>Joh, Jin‐Hyun</au><au>Shin, Sung‐Wook</au><au>Do, Young‐Soo</au><au>Moon, Ji‐Young</au><au>Kim, Na‐Ri</au><au>Lim, Joung‐Eun</au><au>Kim, Ae‐Kyeong</au><au>Eo, Hyun‐Seon</au><au>Kim, Byung‐Soo</au><au>Cho, Seung‐Woo</au><au>Yang, Seung‐Hye</au><au>Park, Chan‐Jeoung</au><au>Shim, Jong‐Sup</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Angiogenesis Facilitated by Autologous Whole Bone Marrow Stem Cell Transplantation for Buerger's Disease</atitle><jtitle>Stem cells (Dayton, Ohio)</jtitle><addtitle>Stem Cells</addtitle><date>2006-05</date><risdate>2006</risdate><volume>24</volume><issue>5</issue><spage>1194</spage><epage>1200</epage><pages>1194-1200</pages><issn>1066-5099</issn><eissn>1549-4918</eissn><abstract>We hypothesized that angiogenesis can be triggered by autologous whole bone marrow stem cell transplantation. Twenty‐seven patients (34 lower limbs) with Buerger's disease, who were not candidates for surgical revascularization or radiologic intervention, were enrolled in this study. Six sites of the tibia bone were fenestrated using a 2.5‐mm‐diameter screw under fluoroscopic guidance. Clinical status and outcome were determined using the “Recommended Standards for Reports.” To mobilize endothelial progenitor cells (EPCs) from bone marrow, recombinant human granulocyte colony‐stimulating factor (r‐HuG‐CSF) was injected subcutaneously as a dose of 75 μg, preoperatively. During the follow‐up period (19.1 ± 3.5 months), one limb showed a markedly improved outcome (+3), and 26 limbs showed a moderately improved outcome (+2). Thirteen limbs among 17 limbs with nonhealing ulcers healed. Postoperative angiograms were obtained for 22 limbs. Two limbs showed marked (+3), five limbs moderate (+2), and nine limbs slight (+1) collateral development. However, six limbs showed no collateral development (0). Peripheral blood and bone marrow samples were analyzed for CD34 and CD133 molecules to enumerate potential EPCs, and EPC numbers were found to be increased in peripheral blood and in bone marrow after r‐HuG‐CSF injection. In conclusion, the transplantation of autologous whole BMCs by fenestration of the tibia bone represents a simple, safe, and effective means of inducing therapeutic angiogenesis in patients with Buerger's disease.</abstract><cop>Bristol</cop><pub>John Wiley & Sons, Ltd</pub><pmid>16439614</pmid><doi>10.1634/stemcells.2005-0349</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Angiogenesis Bone marrow Bone Marrow Cells Female Humans Male Neovascularization, Physiologic Stem Cell Transplantation Stem cells Thromboangiitis Obliterans - therapy Transplantation, Autologous Treatment Outcome |
title | Angiogenesis Facilitated by Autologous Whole Bone Marrow Stem Cell Transplantation for Buerger's Disease |
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