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Predictive Factors of Response to Biological Disease Modifying Antirheumatic Drugs: Towards Personalized Medicine

Many therapies are now available for patients with rheumatoid arthritis (RA) who have an inadequate response to methotrexate including tumor necrosis factor inhibitors, abatacept, tocilizumab, and rituximab. Clinical response to drugs varies widely between individuals. A part of this variability is...

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Detalles Bibliográficos
Autores principales: Daïen, Claire I., Morel, Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913459/
https://www.ncbi.nlm.nih.gov/pubmed/24523570
http://dx.doi.org/10.1155/2014/386148
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author Daïen, Claire I.
Morel, Jacques
author_facet Daïen, Claire I.
Morel, Jacques
author_sort Daïen, Claire I.
collection PubMed
description Many therapies are now available for patients with rheumatoid arthritis (RA) who have an inadequate response to methotrexate including tumor necrosis factor inhibitors, abatacept, tocilizumab, and rituximab. Clinical response to drugs varies widely between individuals. A part of this variability is due to the characteristics of the patient such as age, gender, concomitant therapies, body mass index, or smoking status. Clinical response also depends on disease characteristics including disease activity and severity and presence of autoantibodies. Genetic background, cytokine levels, and immune cell phenotypes could also influence biological therapy response. This review summarizes the impact of all those parameters on response to biological therapies.
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spelling pubmed-39134592014-02-12 Predictive Factors of Response to Biological Disease Modifying Antirheumatic Drugs: Towards Personalized Medicine Daïen, Claire I. Morel, Jacques Mediators Inflamm Review Article Many therapies are now available for patients with rheumatoid arthritis (RA) who have an inadequate response to methotrexate including tumor necrosis factor inhibitors, abatacept, tocilizumab, and rituximab. Clinical response to drugs varies widely between individuals. A part of this variability is due to the characteristics of the patient such as age, gender, concomitant therapies, body mass index, or smoking status. Clinical response also depends on disease characteristics including disease activity and severity and presence of autoantibodies. Genetic background, cytokine levels, and immune cell phenotypes could also influence biological therapy response. This review summarizes the impact of all those parameters on response to biological therapies. Hindawi Publishing Corporation 2014 2014-01-12 /pmc/articles/PMC3913459/ /pubmed/24523570 http://dx.doi.org/10.1155/2014/386148 Text en Copyright © 2014 C. I. Daïen and J. Morel. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Daïen, Claire I.
Morel, Jacques
Predictive Factors of Response to Biological Disease Modifying Antirheumatic Drugs: Towards Personalized Medicine
title Predictive Factors of Response to Biological Disease Modifying Antirheumatic Drugs: Towards Personalized Medicine
title_full Predictive Factors of Response to Biological Disease Modifying Antirheumatic Drugs: Towards Personalized Medicine
title_fullStr Predictive Factors of Response to Biological Disease Modifying Antirheumatic Drugs: Towards Personalized Medicine
title_full_unstemmed Predictive Factors of Response to Biological Disease Modifying Antirheumatic Drugs: Towards Personalized Medicine
title_short Predictive Factors of Response to Biological Disease Modifying Antirheumatic Drugs: Towards Personalized Medicine
title_sort predictive factors of response to biological disease modifying antirheumatic drugs: towards personalized medicine
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913459/
https://www.ncbi.nlm.nih.gov/pubmed/24523570
http://dx.doi.org/10.1155/2014/386148
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