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GM-CSF in inflammation

Granulocyte–macrophage colony-stimulating factor (GM-CSF) has many more functions than its original in vitro identification as an inducer of granulocyte and macrophage development from progenitor cells. Key features of GM-CSF biology need to be defined better, such as the responding and producing ce...

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Detalles Bibliográficos
Autor principal: Hamilton, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037240/
https://www.ncbi.nlm.nih.gov/pubmed/31611249
http://dx.doi.org/10.1084/jem.20190945
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author Hamilton, John A.
author_facet Hamilton, John A.
author_sort Hamilton, John A.
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description Granulocyte–macrophage colony-stimulating factor (GM-CSF) has many more functions than its original in vitro identification as an inducer of granulocyte and macrophage development from progenitor cells. Key features of GM-CSF biology need to be defined better, such as the responding and producing cell types, its links with other mediators, its prosurvival versus activation/differentiation functions, and when it is relevant in pathology. Significant preclinical data have emerged from GM-CSF deletion/depletion approaches indicating that GM-CSF is a potential target in many inflammatory/autoimmune conditions. Clinical trials targeting GM-CSF or its receptor have shown encouraging efficacy and safety profiles, particularly in rheumatoid arthritis. This review provides an update on the above topics and current issues/questions surrounding GM-CSF biology.
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spelling pubmed-70372402020-07-06 GM-CSF in inflammation Hamilton, John A. J Exp Med Reviews Granulocyte–macrophage colony-stimulating factor (GM-CSF) has many more functions than its original in vitro identification as an inducer of granulocyte and macrophage development from progenitor cells. Key features of GM-CSF biology need to be defined better, such as the responding and producing cell types, its links with other mediators, its prosurvival versus activation/differentiation functions, and when it is relevant in pathology. Significant preclinical data have emerged from GM-CSF deletion/depletion approaches indicating that GM-CSF is a potential target in many inflammatory/autoimmune conditions. Clinical trials targeting GM-CSF or its receptor have shown encouraging efficacy and safety profiles, particularly in rheumatoid arthritis. This review provides an update on the above topics and current issues/questions surrounding GM-CSF biology. Rockefeller University Press 2019-10-14 /pmc/articles/PMC7037240/ /pubmed/31611249 http://dx.doi.org/10.1084/jem.20190945 Text en © 2019 Hamilton 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 Reviews
Hamilton, John A.
GM-CSF in inflammation
title GM-CSF in inflammation
title_full GM-CSF in inflammation
title_fullStr GM-CSF in inflammation
title_full_unstemmed GM-CSF in inflammation
title_short GM-CSF in inflammation
title_sort gm-csf in inflammation
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037240/
https://www.ncbi.nlm.nih.gov/pubmed/31611249
http://dx.doi.org/10.1084/jem.20190945
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