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The Treatment of Giant Cell Arteritis in Different Clinical Settings

This paper aims to raise awareness of the different disease courses, comorbidities, and therapy situations in patients with giant cell arteritis (GCA), which require a differentiated approach and often a deviation from current treatment guidelines. With the approval of tocilizumab (TOC), which speci...

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Detalles Bibliográficos
Autores principales: Pfeil, Alexander, Oelzner, Peter, Hellmann, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353794/
https://www.ncbi.nlm.nih.gov/pubmed/30733723
http://dx.doi.org/10.3389/fimmu.2018.03129
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author Pfeil, Alexander
Oelzner, Peter
Hellmann, Peter
author_facet Pfeil, Alexander
Oelzner, Peter
Hellmann, Peter
author_sort Pfeil, Alexander
collection PubMed
description This paper aims to raise awareness of the different disease courses, comorbidities, and therapy situations in patients with giant cell arteritis (GCA), which require a differentiated approach and often a deviation from current treatment guidelines. With the approval of tocilizumab (TOC), which specifically binds to both soluble and membrane-bound IL-6 receptor and inhibits IL-6 receptor-mediated signaling, the spectrum of available effective treatment options has been significantly broadened. TOC yields an extensive range of possible applications that go beyond a glucocorticoid-saving effect. In this context, the treatment of GCA is dependent on the disease course as well as the associated comorbidities. The different stages of GCA in association to co-morbidities require a detailed treatment strategy.
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spelling pubmed-63537942019-02-07 The Treatment of Giant Cell Arteritis in Different Clinical Settings Pfeil, Alexander Oelzner, Peter Hellmann, Peter Front Immunol Immunology This paper aims to raise awareness of the different disease courses, comorbidities, and therapy situations in patients with giant cell arteritis (GCA), which require a differentiated approach and often a deviation from current treatment guidelines. With the approval of tocilizumab (TOC), which specifically binds to both soluble and membrane-bound IL-6 receptor and inhibits IL-6 receptor-mediated signaling, the spectrum of available effective treatment options has been significantly broadened. TOC yields an extensive range of possible applications that go beyond a glucocorticoid-saving effect. In this context, the treatment of GCA is dependent on the disease course as well as the associated comorbidities. The different stages of GCA in association to co-morbidities require a detailed treatment strategy. Frontiers Media S.A. 2019-01-24 /pmc/articles/PMC6353794/ /pubmed/30733723 http://dx.doi.org/10.3389/fimmu.2018.03129 Text en Copyright © 2019 Pfeil, Oelzner and Hellmann. 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
Pfeil, Alexander
Oelzner, Peter
Hellmann, Peter
The Treatment of Giant Cell Arteritis in Different Clinical Settings
title The Treatment of Giant Cell Arteritis in Different Clinical Settings
title_full The Treatment of Giant Cell Arteritis in Different Clinical Settings
title_fullStr The Treatment of Giant Cell Arteritis in Different Clinical Settings
title_full_unstemmed The Treatment of Giant Cell Arteritis in Different Clinical Settings
title_short The Treatment of Giant Cell Arteritis in Different Clinical Settings
title_sort treatment of giant cell arteritis in different clinical settings
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353794/
https://www.ncbi.nlm.nih.gov/pubmed/30733723
http://dx.doi.org/10.3389/fimmu.2018.03129
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