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Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia

Polymorphisms of the cytotoxic T-lymphocyte antigen-4 gene (CTLA-4) have been associated with autoimmune diseases and it has recently been reported that donor genotypes correlate with the outcome of allogeneic hematopoietic stem cell transplantation in leukemia patients. With the aim of confirming t...

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Autores principales: Orrù, Sandro, Orrù, Nicola, Manolakos, Emmanouil, Littera, Roberto, Caocci, Giovanni, Giorgiani, Giovanna, Bertaina, Alice, Pagliara, Daria, Giardini, Claudio, Nesci, Sonia, Locatelli, Franco, Carcassi, Carlo, La Nasa, Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier/North-Holland 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314940/
https://www.ncbi.nlm.nih.gov/pubmed/22245568
http://dx.doi.org/10.1016/j.humimm.2011.12.014
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author Orrù, Sandro
Orrù, Nicola
Manolakos, Emmanouil
Littera, Roberto
Caocci, Giovanni
Giorgiani, Giovanna
Bertaina, Alice
Pagliara, Daria
Giardini, Claudio
Nesci, Sonia
Locatelli, Franco
Carcassi, Carlo
La Nasa, Giorgio
author_facet Orrù, Sandro
Orrù, Nicola
Manolakos, Emmanouil
Littera, Roberto
Caocci, Giovanni
Giorgiani, Giovanna
Bertaina, Alice
Pagliara, Daria
Giardini, Claudio
Nesci, Sonia
Locatelli, Franco
Carcassi, Carlo
La Nasa, Giorgio
author_sort Orrù, Sandro
collection PubMed
description Polymorphisms of the cytotoxic T-lymphocyte antigen-4 gene (CTLA-4) have been associated with autoimmune diseases and it has recently been reported that donor genotypes correlate with the outcome of allogeneic hematopoietic stem cell transplantation in leukemia patients. With the aim of confirming this finding in thalassemia patients, we investigated the influence of genotype distribution of 3 CTLA-4 gene polymorphisms in 72 thalassemia patients and their unrelated donors. A significant association was observed for recipient CT60-AA genotype and onset of grade II–IV (63.2% vs 24.5%; p = 0.001) and grade III–IV (36.4% vs 7.6%; p = 0.005) acute graft-versus-host disease (aGVHD). The same association was observed for the 88-base-pair allele of the CTLA-4 (AT)n polymorphism, which was determined to be in complete linkage disequilibrium with the CT60 A allele. Multinomial Cox regression demonstrated that this association was independent of CT60 donor genotypes or other risk factors (p = 0.016; hazard ratio = 2.8). Our data confirm that the genetic variability in CTLA-4 is an important prognostic factor for aGVHD and suggest that some of the risk factors for this complication are generated by recipient cells that persist after the myeloablative conditioning regimen.
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spelling pubmed-33149402012-04-11 Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia Orrù, Sandro Orrù, Nicola Manolakos, Emmanouil Littera, Roberto Caocci, Giovanni Giorgiani, Giovanna Bertaina, Alice Pagliara, Daria Giardini, Claudio Nesci, Sonia Locatelli, Franco Carcassi, Carlo La Nasa, Giorgio Hum Immunol Article Polymorphisms of the cytotoxic T-lymphocyte antigen-4 gene (CTLA-4) have been associated with autoimmune diseases and it has recently been reported that donor genotypes correlate with the outcome of allogeneic hematopoietic stem cell transplantation in leukemia patients. With the aim of confirming this finding in thalassemia patients, we investigated the influence of genotype distribution of 3 CTLA-4 gene polymorphisms in 72 thalassemia patients and their unrelated donors. A significant association was observed for recipient CT60-AA genotype and onset of grade II–IV (63.2% vs 24.5%; p = 0.001) and grade III–IV (36.4% vs 7.6%; p = 0.005) acute graft-versus-host disease (aGVHD). The same association was observed for the 88-base-pair allele of the CTLA-4 (AT)n polymorphism, which was determined to be in complete linkage disequilibrium with the CT60 A allele. Multinomial Cox regression demonstrated that this association was independent of CT60 donor genotypes or other risk factors (p = 0.016; hazard ratio = 2.8). Our data confirm that the genetic variability in CTLA-4 is an important prognostic factor for aGVHD and suggest that some of the risk factors for this complication are generated by recipient cells that persist after the myeloablative conditioning regimen. Elsevier/North-Holland 2012-03 /pmc/articles/PMC3314940/ /pubmed/22245568 http://dx.doi.org/10.1016/j.humimm.2011.12.014 Text en © 2012 Elsevier Inc. This document may be redistributed and reused, subject to certain conditions (http://www.elsevier.com/wps/find/authorsview.authors/supplementalterms1.0) .
spellingShingle Article
Orrù, Sandro
Orrù, Nicola
Manolakos, Emmanouil
Littera, Roberto
Caocci, Giovanni
Giorgiani, Giovanna
Bertaina, Alice
Pagliara, Daria
Giardini, Claudio
Nesci, Sonia
Locatelli, Franco
Carcassi, Carlo
La Nasa, Giorgio
Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia
title Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia
title_full Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia
title_fullStr Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia
title_full_unstemmed Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia
title_short Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia
title_sort recipient ctla-4*ct60-aa genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314940/
https://www.ncbi.nlm.nih.gov/pubmed/22245568
http://dx.doi.org/10.1016/j.humimm.2011.12.014
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