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De Novo Donor-Specific HLA Antibody Development and Peripheral CD4(+)CD25(high) Cells in Kidney Transplant Recipients: A Place for Interaction?

The aim of this study was to determine whether the abundance of regulatory T cells (Tregs) (CD4(+)CD25(high)) affects the de novo development of anti-HLA donor-specific antibodies (DSAs) in kidney transplant recipients (KTRs). Methods. Unsensitized (PRA ≤ 10%, no DSA) adult primary KTRs who received...

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Autores principales: Alberu, Josefina, Vargas-Rojas, Maria Inés, Morales-Buenrostro, Luis E., Crispin, Jose C., Rodríguez-Romo, Roxana, Uribe-Uribe, Norma O., Carrasco, Gabriel, Gómez-Martín, Diana, Alcocer-Varela, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432543/
https://www.ncbi.nlm.nih.gov/pubmed/22970343
http://dx.doi.org/10.1155/2012/302539
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author Alberu, Josefina
Vargas-Rojas, Maria Inés
Morales-Buenrostro, Luis E.
Crispin, Jose C.
Rodríguez-Romo, Roxana
Uribe-Uribe, Norma O.
Carrasco, Gabriel
Gómez-Martín, Diana
Alcocer-Varela, Jorge
author_facet Alberu, Josefina
Vargas-Rojas, Maria Inés
Morales-Buenrostro, Luis E.
Crispin, Jose C.
Rodríguez-Romo, Roxana
Uribe-Uribe, Norma O.
Carrasco, Gabriel
Gómez-Martín, Diana
Alcocer-Varela, Jorge
author_sort Alberu, Josefina
collection PubMed
description The aim of this study was to determine whether the abundance of regulatory T cells (Tregs) (CD4(+)CD25(high)) affects the de novo development of anti-HLA donor-specific antibodies (DSAs) in kidney transplant recipients (KTRs). Methods. Unsensitized (PRA ≤ 10%, no DSA) adult primary KTRs who received a living (83%) or deceased (17%) KT in our Institution during 2004/2005 were included. DSA testing was performed monthly, and Tregs were quantified by flow cytometry every 3 months, during the 1st year after KT. All patients received triple drug immunosuppressive therapy (CNI + MMF or AZA + PDN); 83% received anti-CD25. Results. 53 KTRs were included; 32% developed DSA during the 1st year after KT. Significantly lower 7-year graft survival was observed in those who developed DSA. No difference was observed in Treg numbers up to 9 months after KT, between DSA positive and negative. However, at 12 months after KT, DSA-negative patients had significantly higher numbers of Treg. Conclusions. Early development of DSA was not associated to variations in Treg abundance. The differences in Treg numbers observed at the late time point may reflect better immune acceptance of the graft and may be associated to long-term effects. Additional inhibitory mechanisms participating earlier in DSA development after KT deserve to be sought.
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spelling pubmed-34325432012-09-11 De Novo Donor-Specific HLA Antibody Development and Peripheral CD4(+)CD25(high) Cells in Kidney Transplant Recipients: A Place for Interaction? Alberu, Josefina Vargas-Rojas, Maria Inés Morales-Buenrostro, Luis E. Crispin, Jose C. Rodríguez-Romo, Roxana Uribe-Uribe, Norma O. Carrasco, Gabriel Gómez-Martín, Diana Alcocer-Varela, Jorge J Transplant Clinical Study The aim of this study was to determine whether the abundance of regulatory T cells (Tregs) (CD4(+)CD25(high)) affects the de novo development of anti-HLA donor-specific antibodies (DSAs) in kidney transplant recipients (KTRs). Methods. Unsensitized (PRA ≤ 10%, no DSA) adult primary KTRs who received a living (83%) or deceased (17%) KT in our Institution during 2004/2005 were included. DSA testing was performed monthly, and Tregs were quantified by flow cytometry every 3 months, during the 1st year after KT. All patients received triple drug immunosuppressive therapy (CNI + MMF or AZA + PDN); 83% received anti-CD25. Results. 53 KTRs were included; 32% developed DSA during the 1st year after KT. Significantly lower 7-year graft survival was observed in those who developed DSA. No difference was observed in Treg numbers up to 9 months after KT, between DSA positive and negative. However, at 12 months after KT, DSA-negative patients had significantly higher numbers of Treg. Conclusions. Early development of DSA was not associated to variations in Treg abundance. The differences in Treg numbers observed at the late time point may reflect better immune acceptance of the graft and may be associated to long-term effects. Additional inhibitory mechanisms participating earlier in DSA development after KT deserve to be sought. Hindawi Publishing Corporation 2012 2012-08-23 /pmc/articles/PMC3432543/ /pubmed/22970343 http://dx.doi.org/10.1155/2012/302539 Text en Copyright © 2012 Josefina Alberu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Alberu, Josefina
Vargas-Rojas, Maria Inés
Morales-Buenrostro, Luis E.
Crispin, Jose C.
Rodríguez-Romo, Roxana
Uribe-Uribe, Norma O.
Carrasco, Gabriel
Gómez-Martín, Diana
Alcocer-Varela, Jorge
De Novo Donor-Specific HLA Antibody Development and Peripheral CD4(+)CD25(high) Cells in Kidney Transplant Recipients: A Place for Interaction?
title De Novo Donor-Specific HLA Antibody Development and Peripheral CD4(+)CD25(high) Cells in Kidney Transplant Recipients: A Place for Interaction?
title_full De Novo Donor-Specific HLA Antibody Development and Peripheral CD4(+)CD25(high) Cells in Kidney Transplant Recipients: A Place for Interaction?
title_fullStr De Novo Donor-Specific HLA Antibody Development and Peripheral CD4(+)CD25(high) Cells in Kidney Transplant Recipients: A Place for Interaction?
title_full_unstemmed De Novo Donor-Specific HLA Antibody Development and Peripheral CD4(+)CD25(high) Cells in Kidney Transplant Recipients: A Place for Interaction?
title_short De Novo Donor-Specific HLA Antibody Development and Peripheral CD4(+)CD25(high) Cells in Kidney Transplant Recipients: A Place for Interaction?
title_sort de novo donor-specific hla antibody development and peripheral cd4(+)cd25(high) cells in kidney transplant recipients: a place for interaction?
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432543/
https://www.ncbi.nlm.nih.gov/pubmed/22970343
http://dx.doi.org/10.1155/2012/302539
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