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Screening for new macrophage therapeutics

Myeloid derived macrophages play a key role in many human diseases, and their therapeutic modulation via pharmacological means is receiving considerable attention. Of particular interest is the fact that these cells are i) dynamic phenotypes well suited to therapeutic manipulation and ii) phagocytic...

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Detalles Bibliográficos
Autores principales: Rodell, Christopher B., Koch, Peter D., Weissleder, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831478/
https://www.ncbi.nlm.nih.gov/pubmed/31695796
http://dx.doi.org/10.7150/thno.34421
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author Rodell, Christopher B.
Koch, Peter D.
Weissleder, Ralph
author_facet Rodell, Christopher B.
Koch, Peter D.
Weissleder, Ralph
author_sort Rodell, Christopher B.
collection PubMed
description Myeloid derived macrophages play a key role in many human diseases, and their therapeutic modulation via pharmacological means is receiving considerable attention. Of particular interest is the fact that these cells are i) dynamic phenotypes well suited to therapeutic manipulation and ii) phagocytic, allowing them to be efficiently targeted with nanoformulations. However, it is important to consider that macrophages represent heterogeneous populations of subtypes with often competing biological behaviors and functions. In order to develop next generation therapeutics, it is therefore essential to screen for biological effects through a combination of in vitro and in vivo assays. Here, we review the state-of-the-art techniques, including both cell based screens and in vivo imaging tools that have been developed for assessment of macrophage phenotype. We conclude with a forward-looking perspective on the growing need for noninvasive macrophage assessment and laboratory assays to be put into clinical practice and the potential broader impact of myeloid-targeted therapeutics.
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spelling pubmed-68314782019-11-06 Screening for new macrophage therapeutics Rodell, Christopher B. Koch, Peter D. Weissleder, Ralph Theranostics Review Myeloid derived macrophages play a key role in many human diseases, and their therapeutic modulation via pharmacological means is receiving considerable attention. Of particular interest is the fact that these cells are i) dynamic phenotypes well suited to therapeutic manipulation and ii) phagocytic, allowing them to be efficiently targeted with nanoformulations. However, it is important to consider that macrophages represent heterogeneous populations of subtypes with often competing biological behaviors and functions. In order to develop next generation therapeutics, it is therefore essential to screen for biological effects through a combination of in vitro and in vivo assays. Here, we review the state-of-the-art techniques, including both cell based screens and in vivo imaging tools that have been developed for assessment of macrophage phenotype. We conclude with a forward-looking perspective on the growing need for noninvasive macrophage assessment and laboratory assays to be put into clinical practice and the potential broader impact of myeloid-targeted therapeutics. Ivyspring International Publisher 2019-10-15 /pmc/articles/PMC6831478/ /pubmed/31695796 http://dx.doi.org/10.7150/thno.34421 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Rodell, Christopher B.
Koch, Peter D.
Weissleder, Ralph
Screening for new macrophage therapeutics
title Screening for new macrophage therapeutics
title_full Screening for new macrophage therapeutics
title_fullStr Screening for new macrophage therapeutics
title_full_unstemmed Screening for new macrophage therapeutics
title_short Screening for new macrophage therapeutics
title_sort screening for new macrophage therapeutics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831478/
https://www.ncbi.nlm.nih.gov/pubmed/31695796
http://dx.doi.org/10.7150/thno.34421
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