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Innate immune pathways and inflammation in hematopoietic aging, clonal hematopoiesis, and MDS

With a growing aged population, there is an imminent need to develop new therapeutic strategies to ameliorate disorders of hematopoietic aging, including clonal hematopoiesis and myelodysplastic syndrome (MDS). Cell-intrinsic dysregulation of innate immune- and inflammatory-related pathways as well...

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Detalles Bibliográficos
Autores principales: Trowbridge, Jennifer J., Starczynowski, Daniel T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210621/
https://www.ncbi.nlm.nih.gov/pubmed/34129017
http://dx.doi.org/10.1084/jem.20201544
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author Trowbridge, Jennifer J.
Starczynowski, Daniel T.
author_facet Trowbridge, Jennifer J.
Starczynowski, Daniel T.
author_sort Trowbridge, Jennifer J.
collection PubMed
description With a growing aged population, there is an imminent need to develop new therapeutic strategies to ameliorate disorders of hematopoietic aging, including clonal hematopoiesis and myelodysplastic syndrome (MDS). Cell-intrinsic dysregulation of innate immune- and inflammatory-related pathways as well as systemic inflammation have been implicated in hematopoietic defects associated with aging, clonal hematopoiesis, and MDS. Here, we review and discuss the role of dysregulated innate immune and inflammatory signaling that contribute to the competitive advantage and clonal dominance of preleukemic and MDS-derived hematopoietic cells. We also propose how emerging concepts will further reveal critical biology and novel therapeutic opportunities.
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spelling pubmed-82106212022-01-05 Innate immune pathways and inflammation in hematopoietic aging, clonal hematopoiesis, and MDS Trowbridge, Jennifer J. Starczynowski, Daniel T. J Exp Med Review With a growing aged population, there is an imminent need to develop new therapeutic strategies to ameliorate disorders of hematopoietic aging, including clonal hematopoiesis and myelodysplastic syndrome (MDS). Cell-intrinsic dysregulation of innate immune- and inflammatory-related pathways as well as systemic inflammation have been implicated in hematopoietic defects associated with aging, clonal hematopoiesis, and MDS. Here, we review and discuss the role of dysregulated innate immune and inflammatory signaling that contribute to the competitive advantage and clonal dominance of preleukemic and MDS-derived hematopoietic cells. We also propose how emerging concepts will further reveal critical biology and novel therapeutic opportunities. Rockefeller University Press 2021-06-15 /pmc/articles/PMC8210621/ /pubmed/34129017 http://dx.doi.org/10.1084/jem.20201544 Text en © 2021 Trowbridge and Starczynowski http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Review
Trowbridge, Jennifer J.
Starczynowski, Daniel T.
Innate immune pathways and inflammation in hematopoietic aging, clonal hematopoiesis, and MDS
title Innate immune pathways and inflammation in hematopoietic aging, clonal hematopoiesis, and MDS
title_full Innate immune pathways and inflammation in hematopoietic aging, clonal hematopoiesis, and MDS
title_fullStr Innate immune pathways and inflammation in hematopoietic aging, clonal hematopoiesis, and MDS
title_full_unstemmed Innate immune pathways and inflammation in hematopoietic aging, clonal hematopoiesis, and MDS
title_short Innate immune pathways and inflammation in hematopoietic aging, clonal hematopoiesis, and MDS
title_sort innate immune pathways and inflammation in hematopoietic aging, clonal hematopoiesis, and mds
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210621/
https://www.ncbi.nlm.nih.gov/pubmed/34129017
http://dx.doi.org/10.1084/jem.20201544
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