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Split Tolerance in a Murine Model of Heterotopic En Bloc Chest Wall Transplantation

BACKGROUND: Congenital and acquired chest wall deformities represent a significant challenge to functional reconstruction and may impact feasibility of heart transplantation for patients with end-stage organ failure. In the recent past, the concept of replacing like-with-like tissue by using vascula...

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Autores principales: Oh, Byoungchol, Furtmüller, Georg J., Malek, Veronika, Fryer, Madeline L., Brayton, Cory, Walczak, Piotr, Janowski, Miroslaw, Brandacher, Gerald, Dorafshar, Amir H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889449/
https://www.ncbi.nlm.nih.gov/pubmed/29632774
http://dx.doi.org/10.1097/GOX.0000000000001595
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author Oh, Byoungchol
Furtmüller, Georg J.
Malek, Veronika
Fryer, Madeline L.
Brayton, Cory
Walczak, Piotr
Janowski, Miroslaw
Brandacher, Gerald
Dorafshar, Amir H.
author_facet Oh, Byoungchol
Furtmüller, Georg J.
Malek, Veronika
Fryer, Madeline L.
Brayton, Cory
Walczak, Piotr
Janowski, Miroslaw
Brandacher, Gerald
Dorafshar, Amir H.
author_sort Oh, Byoungchol
collection PubMed
description BACKGROUND: Congenital and acquired chest wall deformities represent a significant challenge to functional reconstruction and may impact feasibility of heart transplantation for patients with end-stage organ failure. In the recent past, the concept of replacing like-with-like tissue by using vascularized composite allografts (VCA) has been enthusiastically employed for reconstruction of complex tissue defects. METHODS: In this study, we introduce a novel murine model for en bloc chest wall, heart, and thymus transplantation and thereby the use of complex tissue allografts for reconstruction of both chest wall defects and also end-stage organ failure. Additionally, this model allows us to study the features of combined vascularized bone marrow (VBM), thymus, and heart transplantation on allograft survival and function. Heterotopic chest wall, thymus, and heart transplants were performed in untreated syngeneic and allogeneic combinations and in allogeneic combinations treated with costimulation blockade (CTLA4-Ig and MR-1). RESULTS: Indefinite (ie, 150 d, N = 3) graft survival was observed in syngeneic controls. In untreated recipients of allogeneic grafts, the skin component was rejected after 10 (±1) days, whereas rejection of the heart occurred after 13 (± 1) days (N = 3). Costimulation blockade treatment prolonged survival of the heart and chest wall component (130 d, N = 3) as well as the VBM niche as evidenced by donor-specific chimerism (average: 2.35 ± 1.44%), whereas interestingly, the skin component was rejected after 13 (±1) days. CONCLUSION: Thus, this novel microsurgical model of VCA combined with solid organ transplantation is technically feasible and results in split tolerance when treated with costimulatory blockade.
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spelling pubmed-58894492018-04-09 Split Tolerance in a Murine Model of Heterotopic En Bloc Chest Wall Transplantation Oh, Byoungchol Furtmüller, Georg J. Malek, Veronika Fryer, Madeline L. Brayton, Cory Walczak, Piotr Janowski, Miroslaw Brandacher, Gerald Dorafshar, Amir H. Plast Reconstr Surg Glob Open Experimental BACKGROUND: Congenital and acquired chest wall deformities represent a significant challenge to functional reconstruction and may impact feasibility of heart transplantation for patients with end-stage organ failure. In the recent past, the concept of replacing like-with-like tissue by using vascularized composite allografts (VCA) has been enthusiastically employed for reconstruction of complex tissue defects. METHODS: In this study, we introduce a novel murine model for en bloc chest wall, heart, and thymus transplantation and thereby the use of complex tissue allografts for reconstruction of both chest wall defects and also end-stage organ failure. Additionally, this model allows us to study the features of combined vascularized bone marrow (VBM), thymus, and heart transplantation on allograft survival and function. Heterotopic chest wall, thymus, and heart transplants were performed in untreated syngeneic and allogeneic combinations and in allogeneic combinations treated with costimulation blockade (CTLA4-Ig and MR-1). RESULTS: Indefinite (ie, 150 d, N = 3) graft survival was observed in syngeneic controls. In untreated recipients of allogeneic grafts, the skin component was rejected after 10 (±1) days, whereas rejection of the heart occurred after 13 (± 1) days (N = 3). Costimulation blockade treatment prolonged survival of the heart and chest wall component (130 d, N = 3) as well as the VBM niche as evidenced by donor-specific chimerism (average: 2.35 ± 1.44%), whereas interestingly, the skin component was rejected after 13 (±1) days. CONCLUSION: Thus, this novel microsurgical model of VCA combined with solid organ transplantation is technically feasible and results in split tolerance when treated with costimulatory blockade. Wolters Kluwer Health 2017-12-28 /pmc/articles/PMC5889449/ /pubmed/29632774 http://dx.doi.org/10.1097/GOX.0000000000001595 Text en Copyright © 2017 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Experimental
Oh, Byoungchol
Furtmüller, Georg J.
Malek, Veronika
Fryer, Madeline L.
Brayton, Cory
Walczak, Piotr
Janowski, Miroslaw
Brandacher, Gerald
Dorafshar, Amir H.
Split Tolerance in a Murine Model of Heterotopic En Bloc Chest Wall Transplantation
title Split Tolerance in a Murine Model of Heterotopic En Bloc Chest Wall Transplantation
title_full Split Tolerance in a Murine Model of Heterotopic En Bloc Chest Wall Transplantation
title_fullStr Split Tolerance in a Murine Model of Heterotopic En Bloc Chest Wall Transplantation
title_full_unstemmed Split Tolerance in a Murine Model of Heterotopic En Bloc Chest Wall Transplantation
title_short Split Tolerance in a Murine Model of Heterotopic En Bloc Chest Wall Transplantation
title_sort split tolerance in a murine model of heterotopic en bloc chest wall transplantation
topic Experimental
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889449/
https://www.ncbi.nlm.nih.gov/pubmed/29632774
http://dx.doi.org/10.1097/GOX.0000000000001595
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