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Potential for Targeting Myeloid Cells in Controlling CNS Inflammation

Multiple Sclerosis (MS) is characterized by immune cell infiltration to the central nervous system (CNS) as well as loss of myelin. Characterization of the cells in lesions of MS patients revealed an important accumulation of myeloid cells such as macrophages and dendritic cells (DCs). Data from the...

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Detalles Bibliográficos
Autores principales: Ifergan, Igal, Miller, Stephen D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573146/
https://www.ncbi.nlm.nih.gov/pubmed/33123148
http://dx.doi.org/10.3389/fimmu.2020.571897
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author Ifergan, Igal
Miller, Stephen D.
author_facet Ifergan, Igal
Miller, Stephen D.
author_sort Ifergan, Igal
collection PubMed
description Multiple Sclerosis (MS) is characterized by immune cell infiltration to the central nervous system (CNS) as well as loss of myelin. Characterization of the cells in lesions of MS patients revealed an important accumulation of myeloid cells such as macrophages and dendritic cells (DCs). Data from the experimental autoimmune encephalomyelitis (EAE) model of MS supports the importance of peripheral myeloid cells in the disease pathology. However, the majority of MS therapies focus on lymphocytes. As we will discuss in this review, multiple strategies are now in place to target myeloid cells in clinical trials. These strategies have emerged from data in both human and mouse studies. We discuss strategies targeting myeloid cell migration, growth factors and cytokines, biological functions (with a focus on miRNAs), and immunological activities (with a focus on nanoparticles).
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spelling pubmed-75731462020-10-28 Potential for Targeting Myeloid Cells in Controlling CNS Inflammation Ifergan, Igal Miller, Stephen D. Front Immunol Immunology Multiple Sclerosis (MS) is characterized by immune cell infiltration to the central nervous system (CNS) as well as loss of myelin. Characterization of the cells in lesions of MS patients revealed an important accumulation of myeloid cells such as macrophages and dendritic cells (DCs). Data from the experimental autoimmune encephalomyelitis (EAE) model of MS supports the importance of peripheral myeloid cells in the disease pathology. However, the majority of MS therapies focus on lymphocytes. As we will discuss in this review, multiple strategies are now in place to target myeloid cells in clinical trials. These strategies have emerged from data in both human and mouse studies. We discuss strategies targeting myeloid cell migration, growth factors and cytokines, biological functions (with a focus on miRNAs), and immunological activities (with a focus on nanoparticles). Frontiers Media S.A. 2020-10-06 /pmc/articles/PMC7573146/ /pubmed/33123148 http://dx.doi.org/10.3389/fimmu.2020.571897 Text en Copyright © 2020 Ifergan and Miller. 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) and the copyright owner(s) 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
Ifergan, Igal
Miller, Stephen D.
Potential for Targeting Myeloid Cells in Controlling CNS Inflammation
title Potential for Targeting Myeloid Cells in Controlling CNS Inflammation
title_full Potential for Targeting Myeloid Cells in Controlling CNS Inflammation
title_fullStr Potential for Targeting Myeloid Cells in Controlling CNS Inflammation
title_full_unstemmed Potential for Targeting Myeloid Cells in Controlling CNS Inflammation
title_short Potential for Targeting Myeloid Cells in Controlling CNS Inflammation
title_sort potential for targeting myeloid cells in controlling cns inflammation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573146/
https://www.ncbi.nlm.nih.gov/pubmed/33123148
http://dx.doi.org/10.3389/fimmu.2020.571897
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