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T-Cell Costimulatory Molecules in Acute-Graft-Versus Host Disease: Therapeutic Implications

Acute Graft-versus-host disease (GVHD) is a major complication after allogeneic hematopoietic stem cell transplantation. Although this process is thought to consist of several phases, T-cell activation plays a critical role in the pathogenesis of acute GVHD. To become efficient effectors, T-cells re...

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Detalles Bibliográficos
Autores principales: Briones, Javier, Novelli, Silvana, Sierra, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195325/
https://www.ncbi.nlm.nih.gov/pubmed/22046574
http://dx.doi.org/10.1155/2011/976793
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author Briones, Javier
Novelli, Silvana
Sierra, Jorge
author_facet Briones, Javier
Novelli, Silvana
Sierra, Jorge
author_sort Briones, Javier
collection PubMed
description Acute Graft-versus-host disease (GVHD) is a major complication after allogeneic hematopoietic stem cell transplantation. Although this process is thought to consist of several phases, T-cell activation plays a critical role in the pathogenesis of acute GVHD. To become efficient effectors, T-cells require additional costimulation after T-cell receptor signaling. A number of molecules are involved in costimulation of T-cells such as CD28, CD40L, CD30, OX40, 4-1BB, ICOS, and LIGHT. The system is regulated by inhibitory molecules, CTLA-4, and PD-1. There is experimental evidence that those molecules are implicated in the pathogenesis of GHVD. We describe how these molecules are involved in acute GVHD and how the blockade of costimulatory molecules may have potential implications for the treatment of patients with acute GVHD.
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spelling pubmed-31953252011-11-01 T-Cell Costimulatory Molecules in Acute-Graft-Versus Host Disease: Therapeutic Implications Briones, Javier Novelli, Silvana Sierra, Jorge Bone Marrow Res Review Article Acute Graft-versus-host disease (GVHD) is a major complication after allogeneic hematopoietic stem cell transplantation. Although this process is thought to consist of several phases, T-cell activation plays a critical role in the pathogenesis of acute GVHD. To become efficient effectors, T-cells require additional costimulation after T-cell receptor signaling. A number of molecules are involved in costimulation of T-cells such as CD28, CD40L, CD30, OX40, 4-1BB, ICOS, and LIGHT. The system is regulated by inhibitory molecules, CTLA-4, and PD-1. There is experimental evidence that those molecules are implicated in the pathogenesis of GHVD. We describe how these molecules are involved in acute GVHD and how the blockade of costimulatory molecules may have potential implications for the treatment of patients with acute GVHD. Hindawi Publishing Corporation 2011 2010-09-21 /pmc/articles/PMC3195325/ /pubmed/22046574 http://dx.doi.org/10.1155/2011/976793 Text en Copyright © 2011 Javier Briones et al. 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 Review Article
Briones, Javier
Novelli, Silvana
Sierra, Jorge
T-Cell Costimulatory Molecules in Acute-Graft-Versus Host Disease: Therapeutic Implications
title T-Cell Costimulatory Molecules in Acute-Graft-Versus Host Disease: Therapeutic Implications
title_full T-Cell Costimulatory Molecules in Acute-Graft-Versus Host Disease: Therapeutic Implications
title_fullStr T-Cell Costimulatory Molecules in Acute-Graft-Versus Host Disease: Therapeutic Implications
title_full_unstemmed T-Cell Costimulatory Molecules in Acute-Graft-Versus Host Disease: Therapeutic Implications
title_short T-Cell Costimulatory Molecules in Acute-Graft-Versus Host Disease: Therapeutic Implications
title_sort t-cell costimulatory molecules in acute-graft-versus host disease: therapeutic implications
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195325/
https://www.ncbi.nlm.nih.gov/pubmed/22046574
http://dx.doi.org/10.1155/2011/976793
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