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Targeting Macrophages: Friends or Foes in Disease?

Macrophages occupy a prominent position during immune responses. They are considered the final effectors of any given immune response since they can be activated by a wide range of surface ligands and cytokines to acquire a continuum of functional states. Macrophages are involved in tissue homeostas...

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Autores principales: Ardura, Juan A., Rackov, Gorjana, Izquierdo, Elena, Alonso, Veronica, Gortazar, Arancha R., Escribese, Maria M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819424/
https://www.ncbi.nlm.nih.gov/pubmed/31708781
http://dx.doi.org/10.3389/fphar.2019.01255
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author Ardura, Juan A.
Rackov, Gorjana
Izquierdo, Elena
Alonso, Veronica
Gortazar, Arancha R.
Escribese, Maria M.
author_facet Ardura, Juan A.
Rackov, Gorjana
Izquierdo, Elena
Alonso, Veronica
Gortazar, Arancha R.
Escribese, Maria M.
author_sort Ardura, Juan A.
collection PubMed
description Macrophages occupy a prominent position during immune responses. They are considered the final effectors of any given immune response since they can be activated by a wide range of surface ligands and cytokines to acquire a continuum of functional states. Macrophages are involved in tissue homeostasis and in the promotion or resolution of inflammatory responses, causing tissue damage or helping in tissue repair. Knowledge in macrophage polarization has significantly increased in the last decade. Biomarkers, functions, and metabolic states associated with macrophage polarization status have been defined both in murine and human models. Moreover, a large body of evidence demonstrated that macrophage status is a dynamic process that can be modified. Macrophages orchestrate virtually all major diseases—sepsis, infection, chronic inflammatory diseases (rheumatoid arthritis), neurodegenerative disease, and cancer—and thus they represent attractive therapeutic targets. In fact, the possibility to “reprogram” macrophage status is considered as a promising strategy for designing novel therapies. Here, we will review the role of different tissue macrophage populations in the instauration and progression of inflammatory and non-inflammatory pathologies, as exemplified by rheumatoid arthritis, osteoporosis, glioblastoma, and tumor metastasis. We will analyze: 1) the potential as therapeutic targets of recently described macrophage populations, such as osteomacs, reported to play an important role in bone formation and homeostasis or metastasis-associated macrophages (MAMs), key players in the generation of premetastatic niche; 2) the current and potential future approaches to target monocytes/macrophages and their inflammation-causing products in rheumatoid arthritis; and 3) the development of novel intervention strategies using oncolytic viruses, immunomodulatory agents, and checkpoint inhibitors aiming to boost M1-associated anti-tumor immunity. In this review, we will focus on the potential of macrophages as therapeutic targets and discuss their involvement in state-of-the-art strategies to modulate prevalent pathologies of aging societies.
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spelling pubmed-68194242019-11-08 Targeting Macrophages: Friends or Foes in Disease? Ardura, Juan A. Rackov, Gorjana Izquierdo, Elena Alonso, Veronica Gortazar, Arancha R. Escribese, Maria M. Front Pharmacol Pharmacology Macrophages occupy a prominent position during immune responses. They are considered the final effectors of any given immune response since they can be activated by a wide range of surface ligands and cytokines to acquire a continuum of functional states. Macrophages are involved in tissue homeostasis and in the promotion or resolution of inflammatory responses, causing tissue damage or helping in tissue repair. Knowledge in macrophage polarization has significantly increased in the last decade. Biomarkers, functions, and metabolic states associated with macrophage polarization status have been defined both in murine and human models. Moreover, a large body of evidence demonstrated that macrophage status is a dynamic process that can be modified. Macrophages orchestrate virtually all major diseases—sepsis, infection, chronic inflammatory diseases (rheumatoid arthritis), neurodegenerative disease, and cancer—and thus they represent attractive therapeutic targets. In fact, the possibility to “reprogram” macrophage status is considered as a promising strategy for designing novel therapies. Here, we will review the role of different tissue macrophage populations in the instauration and progression of inflammatory and non-inflammatory pathologies, as exemplified by rheumatoid arthritis, osteoporosis, glioblastoma, and tumor metastasis. We will analyze: 1) the potential as therapeutic targets of recently described macrophage populations, such as osteomacs, reported to play an important role in bone formation and homeostasis or metastasis-associated macrophages (MAMs), key players in the generation of premetastatic niche; 2) the current and potential future approaches to target monocytes/macrophages and their inflammation-causing products in rheumatoid arthritis; and 3) the development of novel intervention strategies using oncolytic viruses, immunomodulatory agents, and checkpoint inhibitors aiming to boost M1-associated anti-tumor immunity. In this review, we will focus on the potential of macrophages as therapeutic targets and discuss their involvement in state-of-the-art strategies to modulate prevalent pathologies of aging societies. Frontiers Media S.A. 2019-10-23 /pmc/articles/PMC6819424/ /pubmed/31708781 http://dx.doi.org/10.3389/fphar.2019.01255 Text en Copyright © 2019 Ardura, Rackov, Izquierdo, Alonso, Gortazar and Escribese 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 Pharmacology
Ardura, Juan A.
Rackov, Gorjana
Izquierdo, Elena
Alonso, Veronica
Gortazar, Arancha R.
Escribese, Maria M.
Targeting Macrophages: Friends or Foes in Disease?
title Targeting Macrophages: Friends or Foes in Disease?
title_full Targeting Macrophages: Friends or Foes in Disease?
title_fullStr Targeting Macrophages: Friends or Foes in Disease?
title_full_unstemmed Targeting Macrophages: Friends or Foes in Disease?
title_short Targeting Macrophages: Friends or Foes in Disease?
title_sort targeting macrophages: friends or foes in disease?
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819424/
https://www.ncbi.nlm.nih.gov/pubmed/31708781
http://dx.doi.org/10.3389/fphar.2019.01255
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