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The Role of MicroRNAs in Myeloid Cells during Graft-versus-Host Disease

The successful treatment of various hematologic diseases with allogeneic hematopoietic cell transplantation is often limited by the occurrence of graft-versus-host disease (GvHD). Several microRNAs (miRs) have recently been shown to impact the biology of GvHD by regulating pro- as well as anti-infla...

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Autores principales: Chen, Sophia, Zeiser, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787138/
https://www.ncbi.nlm.nih.gov/pubmed/29410665
http://dx.doi.org/10.3389/fimmu.2018.00004
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author Chen, Sophia
Zeiser, Robert
author_facet Chen, Sophia
Zeiser, Robert
author_sort Chen, Sophia
collection PubMed
description The successful treatment of various hematologic diseases with allogeneic hematopoietic cell transplantation is often limited by the occurrence of graft-versus-host disease (GvHD). Several microRNAs (miRs) have recently been shown to impact the biology of GvHD by regulating pro- as well as anti-inflammatory target genes. There is increasing evidence that a single miR can have different effects by preferentially targeting certain genes depending on the cell type that the miR is analyzed in. This review will focus on the role of miRs in myeloid cells during the development of acute and chronic GvHD and autoimmune diseases. Because miRs act on the expression of multiple target genes and may thereby influence the immune system at different functional levels, they are potentially attractive targets for the modification of allogeneic immune responses using miR mimics and inhibitors.
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spelling pubmed-57871382018-02-06 The Role of MicroRNAs in Myeloid Cells during Graft-versus-Host Disease Chen, Sophia Zeiser, Robert Front Immunol Immunology The successful treatment of various hematologic diseases with allogeneic hematopoietic cell transplantation is often limited by the occurrence of graft-versus-host disease (GvHD). Several microRNAs (miRs) have recently been shown to impact the biology of GvHD by regulating pro- as well as anti-inflammatory target genes. There is increasing evidence that a single miR can have different effects by preferentially targeting certain genes depending on the cell type that the miR is analyzed in. This review will focus on the role of miRs in myeloid cells during the development of acute and chronic GvHD and autoimmune diseases. Because miRs act on the expression of multiple target genes and may thereby influence the immune system at different functional levels, they are potentially attractive targets for the modification of allogeneic immune responses using miR mimics and inhibitors. Frontiers Media S.A. 2018-01-23 /pmc/articles/PMC5787138/ /pubmed/29410665 http://dx.doi.org/10.3389/fimmu.2018.00004 Text en Copyright © 2018 Chen and Zeiser. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Chen, Sophia
Zeiser, Robert
The Role of MicroRNAs in Myeloid Cells during Graft-versus-Host Disease
title The Role of MicroRNAs in Myeloid Cells during Graft-versus-Host Disease
title_full The Role of MicroRNAs in Myeloid Cells during Graft-versus-Host Disease
title_fullStr The Role of MicroRNAs in Myeloid Cells during Graft-versus-Host Disease
title_full_unstemmed The Role of MicroRNAs in Myeloid Cells during Graft-versus-Host Disease
title_short The Role of MicroRNAs in Myeloid Cells during Graft-versus-Host Disease
title_sort role of micrornas in myeloid cells during graft-versus-host disease
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787138/
https://www.ncbi.nlm.nih.gov/pubmed/29410665
http://dx.doi.org/10.3389/fimmu.2018.00004
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