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...

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Veröffentlicht in:Transplantation 2016-12, Vol.100 (12), p.e120-e127
Hauptverfasser: Chang, Jeff, Graves, Scott S, Butts-Miwongtum, Tiffany, Sale, George E, Storb, Rainer, Mathes, David Woodbridge
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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
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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 (&gt;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 (&gt;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 (&gt;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 (&gt;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 (&gt;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 (&gt;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>
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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
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