Long-term Tolerance Toward Haploidentical Vascularized Composite Allograft Transplantation in a Canine Model Using Bone Marrow or Mobilized Stem Cells
BACKGROUNDThe development of safe and reliable protocols for the transplantation of the face and hands may be accomplished with animal modeling of transplantation of vascularized composite allografts (VCA). Previously, we demonstrated that tolerance to a VCA could be achieved after canine recipients...
Gespeichert in:
Veröffentlicht in: | Transplantation 2016-12, Vol.100 (12), p.e120-e127 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e127 |
---|---|
container_issue | 12 |
container_start_page | e120 |
container_title | Transplantation |
container_volume | 100 |
creator | Chang, Jeff Graves, Scott S Butts-Miwongtum, Tiffany Sale, George E Storb, Rainer Mathes, David Woodbridge |
description | BACKGROUNDThe development of safe and reliable protocols for the transplantation of the face and hands may be accomplished with animal modeling of transplantation of vascularized composite allografts (VCA). Previously, we demonstrated that tolerance to a VCA could be achieved after canine recipients were simultaneously given marrow from a dog leukocyte antigen–identical donor. In the present study, we extend those findings across a dog leukocyte antigen mismatched barrier.
METHODSEight recipient dogs received total body irradiation (4.5 cGy), hematopoietic cell transplantation (HCT), either marrow (n = 4) or granulocyte-colony stimulating factor mobilized peripheral blood stem cells (n = 4), and a VCA transplant from the HCT donor. Post grafting immunosuppression consisted of mycophenolate mofetil (28 days) and cyclosporine (35 days).
RESULTSIn 4 dogs receiving bone marrow, 1 accepted both its marrow transplant and demonstrated long-term tolerance to the donor VCA (>52 weeks). Three dogs rejected both their marrow transplants and VCA at 5 to 7 weeks posttransplant. Dogs receiving mobilized stem cells all accepted their stem cell transplant and became tolerant to the VCA. However, 3 dogs developed graft-versus-host disease, whereas 1 dog rejected its stem cell graft by week 15 but exhibited long-term tolerance toward its VCA (>90 weeks).
CONCLUSIONSThe data suggest that simultaneous transplantation of mobilized stem cells and a VCA is feasible and leads to tolerance toward the VCA in a haploidentical setting. However, there is a higher rate of donor stem cell engraftment compared with marrow HCT and an increase in the incidence of graft-versus-host disease. |
doi_str_mv | 10.1097/TP.0000000000001496 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1841801785</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1841801785</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3957-728e9b0ab1de3fb1d6ca7b90111dfdb2ab9942565ff60f6c29c9c96cf4a0cf233</originalsourceid><addsrcrecordid>eNpdkV9v1SAYxolxccfpJzAxXHrTyZ-2lMvZzM3kmC2x87Z5S-EMpVChzYn7IPu8YzvTGCH8e_k9DyQPQu8oOaVEio_d9Sn5p9FS1i_Qhla8LGrSkJdoQ0hJC8q5OEavU_qRoYoL8QodM9HUlEm2Qffb4HfFouOEu-B0BK903u0hjvgSZhfsqP1iFTj8HZJaHUR7p0fchmkOyS4anzkXdhHMgrusTrMDv8Big8fWY8AteOs1_hpG7fBNsn6HP4XHAsQY9jjEfDVY92T6bdETbrVz6Q06MuCSfvu8nqCbz-dde1lsry6-tGfbQnFZiUKwRsuBwEBHzU2eawVikIRSOppxYDBIWbKqroypiakVkyr3WpkSiDKM8xP04eA7x_Br1WnpJ5tU_gF4HdbU06akDaGiqTLKD6iKIaWoTT9HO0H83VPSPwbSd9f9_4Fk1fvnB9Zh0uNfzZ8EMlAegH1wOYb00617HftbDW65ffITjSQFIzTz-VTkwQR_AHPxmHA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1841801785</pqid></control><display><type>article</type><title>Long-term Tolerance Toward Haploidentical Vascularized Composite Allograft Transplantation in a Canine Model Using Bone Marrow or Mobilized Stem Cells</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><creator>Chang, Jeff ; Graves, Scott S ; Butts-Miwongtum, Tiffany ; Sale, George E ; Storb, Rainer ; Mathes, David Woodbridge</creator><creatorcontrib>Chang, Jeff ; Graves, Scott S ; Butts-Miwongtum, Tiffany ; Sale, George E ; Storb, Rainer ; Mathes, David Woodbridge</creatorcontrib><description>BACKGROUNDThe development of safe and reliable protocols for the transplantation of the face and hands may be accomplished with animal modeling of transplantation of vascularized composite allografts (VCA). Previously, we demonstrated that tolerance to a VCA could be achieved after canine recipients were simultaneously given marrow from a dog leukocyte antigen–identical donor. In the present study, we extend those findings across a dog leukocyte antigen mismatched barrier.
METHODSEight recipient dogs received total body irradiation (4.5 cGy), hematopoietic cell transplantation (HCT), either marrow (n = 4) or granulocyte-colony stimulating factor mobilized peripheral blood stem cells (n = 4), and a VCA transplant from the HCT donor. Post grafting immunosuppression consisted of mycophenolate mofetil (28 days) and cyclosporine (35 days).
RESULTSIn 4 dogs receiving bone marrow, 1 accepted both its marrow transplant and demonstrated long-term tolerance to the donor VCA (>52 weeks). Three dogs rejected both their marrow transplants and VCA at 5 to 7 weeks posttransplant. Dogs receiving mobilized stem cells all accepted their stem cell transplant and became tolerant to the VCA. However, 3 dogs developed graft-versus-host disease, whereas 1 dog rejected its stem cell graft by week 15 but exhibited long-term tolerance toward its VCA (>90 weeks).
CONCLUSIONSThe data suggest that simultaneous transplantation of mobilized stem cells and a VCA is feasible and leads to tolerance toward the VCA in a haploidentical setting. However, there is a higher rate of donor stem cell engraftment compared with marrow HCT and an increase in the incidence of graft-versus-host disease.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/TP.0000000000001496</identifier><identifier>PMID: 27861292</identifier><language>eng</language><publisher>United States: Copyright Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Animals ; Antigens - chemistry ; Bone Marrow Cells - metabolism ; Composite Tissue Allografts - immunology ; Cyclosporine - pharmacology ; Dogs ; Graft Rejection - immunology ; Graft Survival ; Graft vs Host Disease ; Granulocyte Colony-Stimulating Factor - pharmacology ; Hematopoietic Stem Cell Mobilization - methods ; Hematopoietic Stem Cell Transplantation ; Immunosuppression Therapy ; Leukocytes - immunology ; Mycophenolic Acid - pharmacology ; Reproducibility of Results ; Skin Transplantation ; Transplantation Conditioning ; Transplantation Tolerance ; Transplantation, Homologous</subject><ispartof>Transplantation, 2016-12, Vol.100 (12), p.e120-e127</ispartof><rights>Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3957-728e9b0ab1de3fb1d6ca7b90111dfdb2ab9942565ff60f6c29c9c96cf4a0cf233</citedby><cites>FETCH-LOGICAL-c3957-728e9b0ab1de3fb1d6ca7b90111dfdb2ab9942565ff60f6c29c9c96cf4a0cf233</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/27861292$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, Jeff</creatorcontrib><creatorcontrib>Graves, Scott S</creatorcontrib><creatorcontrib>Butts-Miwongtum, Tiffany</creatorcontrib><creatorcontrib>Sale, George E</creatorcontrib><creatorcontrib>Storb, Rainer</creatorcontrib><creatorcontrib>Mathes, David Woodbridge</creatorcontrib><title>Long-term Tolerance Toward Haploidentical Vascularized Composite Allograft Transplantation in a Canine Model Using Bone Marrow or Mobilized Stem Cells</title><title>Transplantation</title><addtitle>Transplantation</addtitle><description>BACKGROUNDThe development of safe and reliable protocols for the transplantation of the face and hands may be accomplished with animal modeling of transplantation of vascularized composite allografts (VCA). Previously, we demonstrated that tolerance to a VCA could be achieved after canine recipients were simultaneously given marrow from a dog leukocyte antigen–identical donor. In the present study, we extend those findings across a dog leukocyte antigen mismatched barrier.
METHODSEight recipient dogs received total body irradiation (4.5 cGy), hematopoietic cell transplantation (HCT), either marrow (n = 4) or granulocyte-colony stimulating factor mobilized peripheral blood stem cells (n = 4), and a VCA transplant from the HCT donor. Post grafting immunosuppression consisted of mycophenolate mofetil (28 days) and cyclosporine (35 days).
RESULTSIn 4 dogs receiving bone marrow, 1 accepted both its marrow transplant and demonstrated long-term tolerance to the donor VCA (>52 weeks). Three dogs rejected both their marrow transplants and VCA at 5 to 7 weeks posttransplant. Dogs receiving mobilized stem cells all accepted their stem cell transplant and became tolerant to the VCA. However, 3 dogs developed graft-versus-host disease, whereas 1 dog rejected its stem cell graft by week 15 but exhibited long-term tolerance toward its VCA (>90 weeks).
CONCLUSIONSThe data suggest that simultaneous transplantation of mobilized stem cells and a VCA is feasible and leads to tolerance toward the VCA in a haploidentical setting. However, there is a higher rate of donor stem cell engraftment compared with marrow HCT and an increase in the incidence of graft-versus-host disease.</description><subject>Animals</subject><subject>Antigens - chemistry</subject><subject>Bone Marrow Cells - metabolism</subject><subject>Composite Tissue Allografts - immunology</subject><subject>Cyclosporine - pharmacology</subject><subject>Dogs</subject><subject>Graft Rejection - immunology</subject><subject>Graft Survival</subject><subject>Graft vs Host Disease</subject><subject>Granulocyte Colony-Stimulating Factor - pharmacology</subject><subject>Hematopoietic Stem Cell Mobilization - methods</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Immunosuppression Therapy</subject><subject>Leukocytes - immunology</subject><subject>Mycophenolic Acid - pharmacology</subject><subject>Reproducibility of Results</subject><subject>Skin Transplantation</subject><subject>Transplantation Conditioning</subject><subject>Transplantation Tolerance</subject><subject>Transplantation, Homologous</subject><issn>0041-1337</issn><issn>1534-6080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkV9v1SAYxolxccfpJzAxXHrTyZ-2lMvZzM3kmC2x87Z5S-EMpVChzYn7IPu8YzvTGCH8e_k9DyQPQu8oOaVEio_d9Sn5p9FS1i_Qhla8LGrSkJdoQ0hJC8q5OEavU_qRoYoL8QodM9HUlEm2Qffb4HfFouOEu-B0BK903u0hjvgSZhfsqP1iFTj8HZJaHUR7p0fchmkOyS4anzkXdhHMgrusTrMDv8Big8fWY8AteOs1_hpG7fBNsn6HP4XHAsQY9jjEfDVY92T6bdETbrVz6Q06MuCSfvu8nqCbz-dde1lsry6-tGfbQnFZiUKwRsuBwEBHzU2eawVikIRSOppxYDBIWbKqroypiakVkyr3WpkSiDKM8xP04eA7x_Br1WnpJ5tU_gF4HdbU06akDaGiqTLKD6iKIaWoTT9HO0H83VPSPwbSd9f9_4Fk1fvnB9Zh0uNfzZ8EMlAegH1wOYb00617HftbDW65ffITjSQFIzTz-VTkwQR_AHPxmHA</recordid><startdate>201612</startdate><enddate>201612</enddate><creator>Chang, Jeff</creator><creator>Graves, Scott S</creator><creator>Butts-Miwongtum, Tiffany</creator><creator>Sale, George E</creator><creator>Storb, Rainer</creator><creator>Mathes, David Woodbridge</creator><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</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>7X8</scope></search><sort><creationdate>201612</creationdate><title>Long-term Tolerance Toward Haploidentical Vascularized Composite Allograft Transplantation in a Canine Model Using Bone Marrow or Mobilized Stem Cells</title><author>Chang, Jeff ; Graves, Scott S ; Butts-Miwongtum, Tiffany ; Sale, George E ; Storb, Rainer ; Mathes, David Woodbridge</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3957-728e9b0ab1de3fb1d6ca7b90111dfdb2ab9942565ff60f6c29c9c96cf4a0cf233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Antigens - chemistry</topic><topic>Bone Marrow Cells - metabolism</topic><topic>Composite Tissue Allografts - immunology</topic><topic>Cyclosporine - pharmacology</topic><topic>Dogs</topic><topic>Graft Rejection - immunology</topic><topic>Graft Survival</topic><topic>Graft vs Host Disease</topic><topic>Granulocyte Colony-Stimulating Factor - pharmacology</topic><topic>Hematopoietic Stem Cell Mobilization - methods</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Immunosuppression Therapy</topic><topic>Leukocytes - immunology</topic><topic>Mycophenolic Acid - pharmacology</topic><topic>Reproducibility of Results</topic><topic>Skin Transplantation</topic><topic>Transplantation Conditioning</topic><topic>Transplantation Tolerance</topic><topic>Transplantation, Homologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chang, Jeff</creatorcontrib><creatorcontrib>Graves, Scott S</creatorcontrib><creatorcontrib>Butts-Miwongtum, Tiffany</creatorcontrib><creatorcontrib>Sale, George E</creatorcontrib><creatorcontrib>Storb, Rainer</creatorcontrib><creatorcontrib>Mathes, David Woodbridge</creatorcontrib><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>Transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, Jeff</au><au>Graves, Scott S</au><au>Butts-Miwongtum, Tiffany</au><au>Sale, George E</au><au>Storb, Rainer</au><au>Mathes, David Woodbridge</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term Tolerance Toward Haploidentical Vascularized Composite Allograft Transplantation in a Canine Model Using Bone Marrow or Mobilized Stem Cells</atitle><jtitle>Transplantation</jtitle><addtitle>Transplantation</addtitle><date>2016-12</date><risdate>2016</risdate><volume>100</volume><issue>12</issue><spage>e120</spage><epage>e127</epage><pages>e120-e127</pages><issn>0041-1337</issn><eissn>1534-6080</eissn><abstract>BACKGROUNDThe development of safe and reliable protocols for the transplantation of the face and hands may be accomplished with animal modeling of transplantation of vascularized composite allografts (VCA). Previously, we demonstrated that tolerance to a VCA could be achieved after canine recipients were simultaneously given marrow from a dog leukocyte antigen–identical donor. In the present study, we extend those findings across a dog leukocyte antigen mismatched barrier.
METHODSEight recipient dogs received total body irradiation (4.5 cGy), hematopoietic cell transplantation (HCT), either marrow (n = 4) or granulocyte-colony stimulating factor mobilized peripheral blood stem cells (n = 4), and a VCA transplant from the HCT donor. Post grafting immunosuppression consisted of mycophenolate mofetil (28 days) and cyclosporine (35 days).
RESULTSIn 4 dogs receiving bone marrow, 1 accepted both its marrow transplant and demonstrated long-term tolerance to the donor VCA (>52 weeks). Three dogs rejected both their marrow transplants and VCA at 5 to 7 weeks posttransplant. Dogs receiving mobilized stem cells all accepted their stem cell transplant and became tolerant to the VCA. However, 3 dogs developed graft-versus-host disease, whereas 1 dog rejected its stem cell graft by week 15 but exhibited long-term tolerance toward its VCA (>90 weeks).
CONCLUSIONSThe data suggest that simultaneous transplantation of mobilized stem cells and a VCA is feasible and leads to tolerance toward the VCA in a haploidentical setting. However, there is a higher rate of donor stem cell engraftment compared with marrow HCT and an increase in the incidence of graft-versus-host disease.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>27861292</pmid><doi>10.1097/TP.0000000000001496</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0041-1337 |
ispartof | Transplantation, 2016-12, Vol.100 (12), p.e120-e127 |
issn | 0041-1337 1534-6080 |
language | eng |
recordid | cdi_proquest_miscellaneous_1841801785 |
source | MEDLINE; Journals@Ovid Complete |
subjects | Animals Antigens - chemistry Bone Marrow Cells - metabolism Composite Tissue Allografts - immunology Cyclosporine - pharmacology Dogs Graft Rejection - immunology Graft Survival Graft vs Host Disease Granulocyte Colony-Stimulating Factor - pharmacology Hematopoietic Stem Cell Mobilization - methods Hematopoietic Stem Cell Transplantation Immunosuppression Therapy Leukocytes - immunology Mycophenolic Acid - pharmacology Reproducibility of Results Skin Transplantation Transplantation Conditioning Transplantation Tolerance Transplantation, Homologous |
title | Long-term Tolerance Toward Haploidentical Vascularized Composite Allograft Transplantation in a Canine Model Using Bone Marrow or Mobilized Stem Cells |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T15%3A04%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Long-term%20Tolerance%20Toward%20Haploidentical%20Vascularized%20Composite%20Allograft%20Transplantation%20in%20a%20Canine%20Model%20Using%20Bone%20Marrow%20or%20Mobilized%20Stem%20Cells&rft.jtitle=Transplantation&rft.au=Chang,%20Jeff&rft.date=2016-12&rft.volume=100&rft.issue=12&rft.spage=e120&rft.epage=e127&rft.pages=e120-e127&rft.issn=0041-1337&rft.eissn=1534-6080&rft_id=info:doi/10.1097/TP.0000000000001496&rft_dat=%3Cproquest_cross%3E1841801785%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1841801785&rft_id=info:pmid/27861292&rfr_iscdi=true |