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Myeloid-derived suppressor cells: mechanisms of action and recent advances in their role in transplant tolerance
Myeloid-derived suppressor cells (MDSC) are a heterogeneous population of immature hematopoietic precursors known to suppress immune responses in infection, chronic inflammation, cancer, and autoimmunity. In this paper, we review recent findings detailing their mode of action and discuss recent repo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398399/ https://www.ncbi.nlm.nih.gov/pubmed/22822406 http://dx.doi.org/10.3389/fimmu.2012.00208 |
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author | Dilek, Nahzli Vuillefroy de Silly, Romain Blancho, Gilles Vanhove, Bernard |
author_facet | Dilek, Nahzli Vuillefroy de Silly, Romain Blancho, Gilles Vanhove, Bernard |
author_sort | Dilek, Nahzli |
collection | PubMed |
description | Myeloid-derived suppressor cells (MDSC) are a heterogeneous population of immature hematopoietic precursors known to suppress immune responses in infection, chronic inflammation, cancer, and autoimmunity. In this paper, we review recent findings detailing their mode of action and discuss recent reports that suggest that MDSC are also expanded during transplantation and that modulation of MDSC can participate in preventing graft rejection as well as graft-versus-host disease. |
format | Online Article Text |
id | pubmed-3398399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33983992012-07-20 Myeloid-derived suppressor cells: mechanisms of action and recent advances in their role in transplant tolerance Dilek, Nahzli Vuillefroy de Silly, Romain Blancho, Gilles Vanhove, Bernard Front Immunol Immunology Myeloid-derived suppressor cells (MDSC) are a heterogeneous population of immature hematopoietic precursors known to suppress immune responses in infection, chronic inflammation, cancer, and autoimmunity. In this paper, we review recent findings detailing their mode of action and discuss recent reports that suggest that MDSC are also expanded during transplantation and that modulation of MDSC can participate in preventing graft rejection as well as graft-versus-host disease. Frontiers Research Foundation 2012-07-17 /pmc/articles/PMC3398399/ /pubmed/22822406 http://dx.doi.org/10.3389/fimmu.2012.00208 Text en Copyright © Dilek, Vuillefroy de Silly, Blancho and Vanhove http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits use, distribution, and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any thirdparty graphics etc. |
spellingShingle | Immunology Dilek, Nahzli Vuillefroy de Silly, Romain Blancho, Gilles Vanhove, Bernard Myeloid-derived suppressor cells: mechanisms of action and recent advances in their role in transplant tolerance |
title | Myeloid-derived suppressor cells: mechanisms of action and recent advances in their role in transplant tolerance |
title_full | Myeloid-derived suppressor cells: mechanisms of action and recent advances in their role in transplant tolerance |
title_fullStr | Myeloid-derived suppressor cells: mechanisms of action and recent advances in their role in transplant tolerance |
title_full_unstemmed | Myeloid-derived suppressor cells: mechanisms of action and recent advances in their role in transplant tolerance |
title_short | Myeloid-derived suppressor cells: mechanisms of action and recent advances in their role in transplant tolerance |
title_sort | myeloid-derived suppressor cells: mechanisms of action and recent advances in their role in transplant tolerance |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398399/ https://www.ncbi.nlm.nih.gov/pubmed/22822406 http://dx.doi.org/10.3389/fimmu.2012.00208 |
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