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From Immune Dysregulations to Therapeutic Perspectives in Myelodysplastic Syndromes: A Review

The pathophysiology of myelodysplastic syndromes (MDSs) is complex and often includes immune dysregulation of both the innate and adaptive immune systems. Whereas clonal selection mainly involves smoldering inflammation, a cellular immunity dysfunction leads to increased apoptosis and blast prolifer...

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Detalles Bibliográficos
Autores principales: Comont, Thibault, Treiner, Emmanuel, Vergez, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620222/
https://www.ncbi.nlm.nih.gov/pubmed/34829329
http://dx.doi.org/10.3390/diagnostics11111982
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author Comont, Thibault
Treiner, Emmanuel
Vergez, François
author_facet Comont, Thibault
Treiner, Emmanuel
Vergez, François
author_sort Comont, Thibault
collection PubMed
description The pathophysiology of myelodysplastic syndromes (MDSs) is complex and often includes immune dysregulation of both the innate and adaptive immune systems. Whereas clonal selection mainly involves smoldering inflammation, a cellular immunity dysfunction leads to increased apoptosis and blast proliferation. Addressing immune dysregulations in MDS is a recent concept that has allowed the identification of new therapeutic targets. Several approaches targeting the different actors of the immune system have therefore been developed. However, the results are very heterogeneous, indicating the need to improve our understanding of the disease and interactions between chronic inflammation, adaptive dysfunction, and somatic mutations. This review highlights current knowledge of the role of immune dysregulation in MDS pathophysiology and the field of new drugs.
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spelling pubmed-86202222021-11-27 From Immune Dysregulations to Therapeutic Perspectives in Myelodysplastic Syndromes: A Review Comont, Thibault Treiner, Emmanuel Vergez, François Diagnostics (Basel) Review The pathophysiology of myelodysplastic syndromes (MDSs) is complex and often includes immune dysregulation of both the innate and adaptive immune systems. Whereas clonal selection mainly involves smoldering inflammation, a cellular immunity dysfunction leads to increased apoptosis and blast proliferation. Addressing immune dysregulations in MDS is a recent concept that has allowed the identification of new therapeutic targets. Several approaches targeting the different actors of the immune system have therefore been developed. However, the results are very heterogeneous, indicating the need to improve our understanding of the disease and interactions between chronic inflammation, adaptive dysfunction, and somatic mutations. This review highlights current knowledge of the role of immune dysregulation in MDS pathophysiology and the field of new drugs. MDPI 2021-10-26 /pmc/articles/PMC8620222/ /pubmed/34829329 http://dx.doi.org/10.3390/diagnostics11111982 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Comont, Thibault
Treiner, Emmanuel
Vergez, François
From Immune Dysregulations to Therapeutic Perspectives in Myelodysplastic Syndromes: A Review
title From Immune Dysregulations to Therapeutic Perspectives in Myelodysplastic Syndromes: A Review
title_full From Immune Dysregulations to Therapeutic Perspectives in Myelodysplastic Syndromes: A Review
title_fullStr From Immune Dysregulations to Therapeutic Perspectives in Myelodysplastic Syndromes: A Review
title_full_unstemmed From Immune Dysregulations to Therapeutic Perspectives in Myelodysplastic Syndromes: A Review
title_short From Immune Dysregulations to Therapeutic Perspectives in Myelodysplastic Syndromes: A Review
title_sort from immune dysregulations to therapeutic perspectives in myelodysplastic syndromes: a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620222/
https://www.ncbi.nlm.nih.gov/pubmed/34829329
http://dx.doi.org/10.3390/diagnostics11111982
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