Experimental Assessment of Intestinal Damage in Controlled Donation After Circulatory Death for Visceral Transplantation

Autores
Stringa, Pablo Luis; Vecchio Dezillio, Leandro Emmanuel; Talayero, Paloma; Serradilla, Javier; Errea, Agustina Juliana; Papa Gobbi, Rodrigo; Camps Ortega, Onys; Pucci Molineris, Melisa Eliana; Lausada, Natalia Raquel; Andres Moreno, Ane Miren; Rumbo, Martín; Hernández Oliveros, Francisco
Año de publicación
2023
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
There is an urgent need to address the shortage of potential multivisceral grafts in order to reduce the average time in waiting list. Since donation after circulatory death (DCD) has been successfully employed for other solid organs, a thorough evaluation of the use of intestinal grafts from DCD is warranted. Here, we have generated a model of Maastricht III DCD in rodents, focusing on the viability of intestinal and multivisceral grafts at five (DCD5) and twenty (DCD20) minutes of cardiac arrest compared to living and brain death donors. DCD groups exhibited time-dependent damage. DCD20 generated substantial intestinal mucosal injury and decreased number of Goblet cells whereas grafts from DCD5 closely resemble those of brain death and living donors groups in terms intestinal morphology, expression of tight junction proteins and number of Paneth and Globet cells. Upon transplantation, intestines from DCD5 showed increased ischemia/reperfusion damage compared to living donor grafts, however mucosal integrity was recovered 48 h after transplantation. No differences in terms of graft rejection, gene expression and absorptive function between DCD5 and living donor were observed at 7 post-transplant days. Collectively, our results highlight DCD as a possible strategy to increase multivisceral donation and transplantation procedures.
Instituto de Estudios Inmunológicos y Fisiopatológicos
Consejo Nacional de Investigaciones Científicas y Técnicas
Materia
Ciencias Médicas
donation after cardiac death
experimental transplantation
intestinal transplantation
organ procurement
solid organ transplant
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/162848

id SEDICI_dd45639d59b704aeafe68244af4a2a68
oai_identifier_str oai:sedici.unlp.edu.ar:10915/162848
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Experimental Assessment of Intestinal Damage in Controlled Donation After Circulatory Death for Visceral TransplantationStringa, Pablo LuisVecchio Dezillio, Leandro EmmanuelTalayero, PalomaSerradilla, JavierErrea, Agustina JulianaPapa Gobbi, RodrigoCamps Ortega, OnysPucci Molineris, Melisa ElianaLausada, Natalia RaquelAndres Moreno, Ane MirenRumbo, MartínHernández Oliveros, FranciscoCiencias Médicasdonation after cardiac deathexperimental transplantationintestinal transplantationorgan procurementsolid organ transplantThere is an urgent need to address the shortage of potential multivisceral grafts in order to reduce the average time in waiting list. Since donation after circulatory death (DCD) has been successfully employed for other solid organs, a thorough evaluation of the use of intestinal grafts from DCD is warranted. Here, we have generated a model of Maastricht III DCD in rodents, focusing on the viability of intestinal and multivisceral grafts at five (DCD5) and twenty (DCD20) minutes of cardiac arrest compared to living and brain death donors. DCD groups exhibited time-dependent damage. DCD20 generated substantial intestinal mucosal injury and decreased number of Goblet cells whereas grafts from DCD5 closely resemble those of brain death and living donors groups in terms intestinal morphology, expression of tight junction proteins and number of Paneth and Globet cells. Upon transplantation, intestines from DCD5 showed increased ischemia/reperfusion damage compared to living donor grafts, however mucosal integrity was recovered 48 h after transplantation. No differences in terms of graft rejection, gene expression and absorptive function between DCD5 and living donor were observed at 7 post-transplant days. Collectively, our results highlight DCD as a possible strategy to increase multivisceral donation and transplantation procedures.Instituto de Estudios Inmunológicos y FisiopatológicosConsejo Nacional de Investigaciones Científicas y Técnicas2023-01-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/162848enginfo:eu-repo/semantics/altIdentifier/issn/1432-2277info:eu-repo/semantics/altIdentifier/doi/10.3389/ti.2023.10803info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T11:14:42Zoai:sedici.unlp.edu.ar:10915/162848Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 11:14:42.784SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Experimental Assessment of Intestinal Damage in Controlled Donation After Circulatory Death for Visceral Transplantation
title Experimental Assessment of Intestinal Damage in Controlled Donation After Circulatory Death for Visceral Transplantation
spellingShingle Experimental Assessment of Intestinal Damage in Controlled Donation After Circulatory Death for Visceral Transplantation
Stringa, Pablo Luis
Ciencias Médicas
donation after cardiac death
experimental transplantation
intestinal transplantation
organ procurement
solid organ transplant
title_short Experimental Assessment of Intestinal Damage in Controlled Donation After Circulatory Death for Visceral Transplantation
title_full Experimental Assessment of Intestinal Damage in Controlled Donation After Circulatory Death for Visceral Transplantation
title_fullStr Experimental Assessment of Intestinal Damage in Controlled Donation After Circulatory Death for Visceral Transplantation
title_full_unstemmed Experimental Assessment of Intestinal Damage in Controlled Donation After Circulatory Death for Visceral Transplantation
title_sort Experimental Assessment of Intestinal Damage in Controlled Donation After Circulatory Death for Visceral Transplantation
dc.creator.none.fl_str_mv Stringa, Pablo Luis
Vecchio Dezillio, Leandro Emmanuel
Talayero, Paloma
Serradilla, Javier
Errea, Agustina Juliana
Papa Gobbi, Rodrigo
Camps Ortega, Onys
Pucci Molineris, Melisa Eliana
Lausada, Natalia Raquel
Andres Moreno, Ane Miren
Rumbo, Martín
Hernández Oliveros, Francisco
author Stringa, Pablo Luis
author_facet Stringa, Pablo Luis
Vecchio Dezillio, Leandro Emmanuel
Talayero, Paloma
Serradilla, Javier
Errea, Agustina Juliana
Papa Gobbi, Rodrigo
Camps Ortega, Onys
Pucci Molineris, Melisa Eliana
Lausada, Natalia Raquel
Andres Moreno, Ane Miren
Rumbo, Martín
Hernández Oliveros, Francisco
author_role author
author2 Vecchio Dezillio, Leandro Emmanuel
Talayero, Paloma
Serradilla, Javier
Errea, Agustina Juliana
Papa Gobbi, Rodrigo
Camps Ortega, Onys
Pucci Molineris, Melisa Eliana
Lausada, Natalia Raquel
Andres Moreno, Ane Miren
Rumbo, Martín
Hernández Oliveros, Francisco
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Ciencias Médicas
donation after cardiac death
experimental transplantation
intestinal transplantation
organ procurement
solid organ transplant
topic Ciencias Médicas
donation after cardiac death
experimental transplantation
intestinal transplantation
organ procurement
solid organ transplant
dc.description.none.fl_txt_mv There is an urgent need to address the shortage of potential multivisceral grafts in order to reduce the average time in waiting list. Since donation after circulatory death (DCD) has been successfully employed for other solid organs, a thorough evaluation of the use of intestinal grafts from DCD is warranted. Here, we have generated a model of Maastricht III DCD in rodents, focusing on the viability of intestinal and multivisceral grafts at five (DCD5) and twenty (DCD20) minutes of cardiac arrest compared to living and brain death donors. DCD groups exhibited time-dependent damage. DCD20 generated substantial intestinal mucosal injury and decreased number of Goblet cells whereas grafts from DCD5 closely resemble those of brain death and living donors groups in terms intestinal morphology, expression of tight junction proteins and number of Paneth and Globet cells. Upon transplantation, intestines from DCD5 showed increased ischemia/reperfusion damage compared to living donor grafts, however mucosal integrity was recovered 48 h after transplantation. No differences in terms of graft rejection, gene expression and absorptive function between DCD5 and living donor were observed at 7 post-transplant days. Collectively, our results highlight DCD as a possible strategy to increase multivisceral donation and transplantation procedures.
Instituto de Estudios Inmunológicos y Fisiopatológicos
Consejo Nacional de Investigaciones Científicas y Técnicas
description There is an urgent need to address the shortage of potential multivisceral grafts in order to reduce the average time in waiting list. Since donation after circulatory death (DCD) has been successfully employed for other solid organs, a thorough evaluation of the use of intestinal grafts from DCD is warranted. Here, we have generated a model of Maastricht III DCD in rodents, focusing on the viability of intestinal and multivisceral grafts at five (DCD5) and twenty (DCD20) minutes of cardiac arrest compared to living and brain death donors. DCD groups exhibited time-dependent damage. DCD20 generated substantial intestinal mucosal injury and decreased number of Goblet cells whereas grafts from DCD5 closely resemble those of brain death and living donors groups in terms intestinal morphology, expression of tight junction proteins and number of Paneth and Globet cells. Upon transplantation, intestines from DCD5 showed increased ischemia/reperfusion damage compared to living donor grafts, however mucosal integrity was recovered 48 h after transplantation. No differences in terms of graft rejection, gene expression and absorptive function between DCD5 and living donor were observed at 7 post-transplant days. Collectively, our results highlight DCD as a possible strategy to increase multivisceral donation and transplantation procedures.
publishDate 2023
dc.date.none.fl_str_mv 2023-01-12
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/162848
url http://sedici.unlp.edu.ar/handle/10915/162848
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/1432-2277
info:eu-repo/semantics/altIdentifier/doi/10.3389/ti.2023.10803
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
_version_ 1842260652113002496
score 13.13397