Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation
- Autores
- Cicora, Federico; Roberti, Javier Eugenio; Lausada, Natalia Raquel; González, Pedro Horacio; Guerrieri, Diego; Stringa, Pablo Luis; Cicora, Paola; Vásquez, Daniela; González, Ivana; Palti, Gustavo; Intile, Dante; Raimondi, Clemente
- Año de publicación
- 2012
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- A major concern in transplantation is the preservation of organ function. Ischemia time and microcirculatory disturbance of the organ cannot be avoided and may result in ischemia reperfusion injury (IRI), increasing the risk of delayed graft function (DGF) and acute and chronic rejection. Anti-thymocyte immunoglobulin (rATG) is a polyclonal antibody preparation with multiple effects when administered to recipients. Our objective has been to evaluate whether the administration of rATG to kidney donors instead of recipients, in an experimental model of syngeneic rat transplantation, ameliorates IRI and facilitates immediate graft function recovery. Urea and creatinine levels and necrosis severity scores were significantly lower in kidneys from donors that had received rATG (urea: control: 211 ± 8. mg/dl vs. treatment: 110 ± 15. mg/dl, p < 0.001; creatinine: control: 4.6 ± 0.24. mg/dl vs. treatment: 2.6 ± 0.22. mg/dl, p < 0.001; necrosis severity scores: control: 2.3 vs. treatment: 1.6, p < 0.05). TUNEL staining showed 80 ± 13 positive cells in control group and 9 ± 3 (p < 0.001) in treatment group. In situ expression of proinflammatory cytokines TNF-α, IL-6, IL-21 and TGF-β1 was reduced in rATG group (p < 0.01); the same was observed for KIM-1 and caspase 8 (p < 0.001). Cytoprotective genes Bcl2 and HO-1 were upregulated in situ in treatment group (p < 0.001). In situ expression of IL-17, caspase 9, IL-23a, CxCl3 and ICAM1 showed no difference between groups (p > 0.05). Findings suggest ATG administered to donors may ameliorate the IRI process in kidney transplantation, expressed by lower necrosis and apoptosis scores and the improvement of renal function, which may be explained through the diminished in situ expression of inflammatory mediators.
Fil: Cicora, Federico. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina. Hospital Aleman; Argentina
Fil: Roberti, Javier Eugenio. Universidad de Belgrano; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Lausada, Natalia Raquel. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina
Fil: González, Pedro Horacio. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas; Argentina
Fil: Guerrieri, Diego. Universidad de Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Stringa, Pablo Luis. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Cicora, Paola. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; Argentina
Fil: Vásquez, Daniela. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; Argentina
Fil: González, Ivana. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; Argentina
Fil: Palti, Gustavo. Hospital Alemán; Argentina
Fil: Intile, Dante. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; Argentina
Fil: Raimondi, Clemente. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina - Materia
-
KIDNEY TRANSPLANTATION
DONOR PRECONDITIONING
APOPTOSIS
ISCHEMIA REPERFUSION INJURY - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/245828
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Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantationCicora, FedericoRoberti, Javier EugenioLausada, Natalia RaquelGonzález, Pedro HoracioGuerrieri, DiegoStringa, Pablo LuisCicora, PaolaVásquez, DanielaGonzález, IvanaPalti, GustavoIntile, DanteRaimondi, ClementeKIDNEY TRANSPLANTATIONDONOR PRECONDITIONINGAPOPTOSISISCHEMIA REPERFUSION INJURYhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3A major concern in transplantation is the preservation of organ function. Ischemia time and microcirculatory disturbance of the organ cannot be avoided and may result in ischemia reperfusion injury (IRI), increasing the risk of delayed graft function (DGF) and acute and chronic rejection. Anti-thymocyte immunoglobulin (rATG) is a polyclonal antibody preparation with multiple effects when administered to recipients. Our objective has been to evaluate whether the administration of rATG to kidney donors instead of recipients, in an experimental model of syngeneic rat transplantation, ameliorates IRI and facilitates immediate graft function recovery. Urea and creatinine levels and necrosis severity scores were significantly lower in kidneys from donors that had received rATG (urea: control: 211 ± 8. mg/dl vs. treatment: 110 ± 15. mg/dl, p < 0.001; creatinine: control: 4.6 ± 0.24. mg/dl vs. treatment: 2.6 ± 0.22. mg/dl, p < 0.001; necrosis severity scores: control: 2.3 vs. treatment: 1.6, p < 0.05). TUNEL staining showed 80 ± 13 positive cells in control group and 9 ± 3 (p < 0.001) in treatment group. In situ expression of proinflammatory cytokines TNF-α, IL-6, IL-21 and TGF-β1 was reduced in rATG group (p < 0.01); the same was observed for KIM-1 and caspase 8 (p < 0.001). Cytoprotective genes Bcl2 and HO-1 were upregulated in situ in treatment group (p < 0.001). In situ expression of IL-17, caspase 9, IL-23a, CxCl3 and ICAM1 showed no difference between groups (p > 0.05). Findings suggest ATG administered to donors may ameliorate the IRI process in kidney transplantation, expressed by lower necrosis and apoptosis scores and the improvement of renal function, which may be explained through the diminished in situ expression of inflammatory mediators.Fil: Cicora, Federico. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina. Hospital Aleman; ArgentinaFil: Roberti, Javier Eugenio. Universidad de Belgrano; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Lausada, Natalia Raquel. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; ArgentinaFil: González, Pedro Horacio. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas; ArgentinaFil: Guerrieri, Diego. Universidad de Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Stringa, Pablo Luis. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Cicora, Paola. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; ArgentinaFil: Vásquez, Daniela. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; ArgentinaFil: González, Ivana. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; ArgentinaFil: Palti, Gustavo. Hospital Alemán; ArgentinaFil: Intile, Dante. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; ArgentinaFil: Raimondi, Clemente. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; ArgentinaElsevier Science2012-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/245828Cicora, Federico; Roberti, Javier Eugenio; Lausada, Natalia Raquel; González, Pedro Horacio; Guerrieri, Diego; et al.; Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation; Elsevier Science; Transplant Immunology; 27; 1; 8-2012; 1-70966-3274CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0966327412000275info:eu-repo/semantics/altIdentifier/doi/10.1016/j.trim.2012.03.004info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:54:11Zoai:ri.conicet.gov.ar:11336/245828instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:54:11.82CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation |
title |
Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation |
spellingShingle |
Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation Cicora, Federico KIDNEY TRANSPLANTATION DONOR PRECONDITIONING APOPTOSIS ISCHEMIA REPERFUSION INJURY |
title_short |
Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation |
title_full |
Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation |
title_fullStr |
Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation |
title_full_unstemmed |
Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation |
title_sort |
Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation |
dc.creator.none.fl_str_mv |
Cicora, Federico Roberti, Javier Eugenio Lausada, Natalia Raquel González, Pedro Horacio Guerrieri, Diego Stringa, Pablo Luis Cicora, Paola Vásquez, Daniela González, Ivana Palti, Gustavo Intile, Dante Raimondi, Clemente |
author |
Cicora, Federico |
author_facet |
Cicora, Federico Roberti, Javier Eugenio Lausada, Natalia Raquel González, Pedro Horacio Guerrieri, Diego Stringa, Pablo Luis Cicora, Paola Vásquez, Daniela González, Ivana Palti, Gustavo Intile, Dante Raimondi, Clemente |
author_role |
author |
author2 |
Roberti, Javier Eugenio Lausada, Natalia Raquel González, Pedro Horacio Guerrieri, Diego Stringa, Pablo Luis Cicora, Paola Vásquez, Daniela González, Ivana Palti, Gustavo Intile, Dante Raimondi, Clemente |
author2_role |
author author author author author author author author author author author |
dc.subject.none.fl_str_mv |
KIDNEY TRANSPLANTATION DONOR PRECONDITIONING APOPTOSIS ISCHEMIA REPERFUSION INJURY |
topic |
KIDNEY TRANSPLANTATION DONOR PRECONDITIONING APOPTOSIS ISCHEMIA REPERFUSION INJURY |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
A major concern in transplantation is the preservation of organ function. Ischemia time and microcirculatory disturbance of the organ cannot be avoided and may result in ischemia reperfusion injury (IRI), increasing the risk of delayed graft function (DGF) and acute and chronic rejection. Anti-thymocyte immunoglobulin (rATG) is a polyclonal antibody preparation with multiple effects when administered to recipients. Our objective has been to evaluate whether the administration of rATG to kidney donors instead of recipients, in an experimental model of syngeneic rat transplantation, ameliorates IRI and facilitates immediate graft function recovery. Urea and creatinine levels and necrosis severity scores were significantly lower in kidneys from donors that had received rATG (urea: control: 211 ± 8. mg/dl vs. treatment: 110 ± 15. mg/dl, p < 0.001; creatinine: control: 4.6 ± 0.24. mg/dl vs. treatment: 2.6 ± 0.22. mg/dl, p < 0.001; necrosis severity scores: control: 2.3 vs. treatment: 1.6, p < 0.05). TUNEL staining showed 80 ± 13 positive cells in control group and 9 ± 3 (p < 0.001) in treatment group. In situ expression of proinflammatory cytokines TNF-α, IL-6, IL-21 and TGF-β1 was reduced in rATG group (p < 0.01); the same was observed for KIM-1 and caspase 8 (p < 0.001). Cytoprotective genes Bcl2 and HO-1 were upregulated in situ in treatment group (p < 0.001). In situ expression of IL-17, caspase 9, IL-23a, CxCl3 and ICAM1 showed no difference between groups (p > 0.05). Findings suggest ATG administered to donors may ameliorate the IRI process in kidney transplantation, expressed by lower necrosis and apoptosis scores and the improvement of renal function, which may be explained through the diminished in situ expression of inflammatory mediators. Fil: Cicora, Federico. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina. Hospital Aleman; Argentina Fil: Roberti, Javier Eugenio. Universidad de Belgrano; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Lausada, Natalia Raquel. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina Fil: González, Pedro Horacio. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas; Argentina Fil: Guerrieri, Diego. Universidad de Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Stringa, Pablo Luis. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Cicora, Paola. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; Argentina Fil: Vásquez, Daniela. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; Argentina Fil: González, Ivana. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; Argentina Fil: Palti, Gustavo. Hospital Alemán; Argentina Fil: Intile, Dante. Fundación Para la Investigación y Asistencia de la Enfermedad Renal; Argentina Fil: Raimondi, Clemente. Universidad Nacional de La Plata. Facultad de Ciencias Médicas; Argentina |
description |
A major concern in transplantation is the preservation of organ function. Ischemia time and microcirculatory disturbance of the organ cannot be avoided and may result in ischemia reperfusion injury (IRI), increasing the risk of delayed graft function (DGF) and acute and chronic rejection. Anti-thymocyte immunoglobulin (rATG) is a polyclonal antibody preparation with multiple effects when administered to recipients. Our objective has been to evaluate whether the administration of rATG to kidney donors instead of recipients, in an experimental model of syngeneic rat transplantation, ameliorates IRI and facilitates immediate graft function recovery. Urea and creatinine levels and necrosis severity scores were significantly lower in kidneys from donors that had received rATG (urea: control: 211 ± 8. mg/dl vs. treatment: 110 ± 15. mg/dl, p < 0.001; creatinine: control: 4.6 ± 0.24. mg/dl vs. treatment: 2.6 ± 0.22. mg/dl, p < 0.001; necrosis severity scores: control: 2.3 vs. treatment: 1.6, p < 0.05). TUNEL staining showed 80 ± 13 positive cells in control group and 9 ± 3 (p < 0.001) in treatment group. In situ expression of proinflammatory cytokines TNF-α, IL-6, IL-21 and TGF-β1 was reduced in rATG group (p < 0.01); the same was observed for KIM-1 and caspase 8 (p < 0.001). Cytoprotective genes Bcl2 and HO-1 were upregulated in situ in treatment group (p < 0.001). In situ expression of IL-17, caspase 9, IL-23a, CxCl3 and ICAM1 showed no difference between groups (p > 0.05). Findings suggest ATG administered to donors may ameliorate the IRI process in kidney transplantation, expressed by lower necrosis and apoptosis scores and the improvement of renal function, which may be explained through the diminished in situ expression of inflammatory mediators. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-08 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion 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://hdl.handle.net/11336/245828 Cicora, Federico; Roberti, Javier Eugenio; Lausada, Natalia Raquel; González, Pedro Horacio; Guerrieri, Diego; et al.; Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation; Elsevier Science; Transplant Immunology; 27; 1; 8-2012; 1-7 0966-3274 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/245828 |
identifier_str_mv |
Cicora, Federico; Roberti, Javier Eugenio; Lausada, Natalia Raquel; González, Pedro Horacio; Guerrieri, Diego; et al.; Donor preconditioning with rabbit anti-rat thymocyte immunoglobulin ameliorates ischemia reperfusion injury in rat kidney transplantation; Elsevier Science; Transplant Immunology; 27; 1; 8-2012; 1-7 0966-3274 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0966327412000275 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.trim.2012.03.004 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier Science |
publisher.none.fl_str_mv |
Elsevier Science |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
_version_ |
1842269270646456320 |
score |
13.13397 |