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Optimizing the use of biological therapy in patients with inflammatory bowel disease

Biological therapy revolutionized the treatment of inflammatory bowel disease (IBD) during the last decade. These monoclonal antibodies, which target tumor necrosis factor (TNF), integrins or IL12/23, have been approved—or are in development for—both Crohn’s disease (CD) and ulcerative colitis (UC)....

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Detalles Bibliográficos
Autor principal: Moss, Alan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4324872/
https://www.ncbi.nlm.nih.gov/pubmed/25567472
http://dx.doi.org/10.1093/gastro/gou087
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author Moss, Alan C.
author_facet Moss, Alan C.
author_sort Moss, Alan C.
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description Biological therapy revolutionized the treatment of inflammatory bowel disease (IBD) during the last decade. These monoclonal antibodies, which target tumor necrosis factor (TNF), integrins or IL12/23, have been approved—or are in development for—both Crohn’s disease (CD) and ulcerative colitis (UC). Early use of these agents taught clinicians that induction and maintenance therapy, coupled with immunomodulator agents, reduced the immunogenicity of these agents, and led to sustained remission in many patients. More recent data has demonstrated that, through dose adjustments, optimizing serum drug levels may also provide more durable maintenance of remission, and improved mucosal healing. This review examines clinical practices that may enhance clinical outcomes from biological therapy in IBD.
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spelling pubmed-43248722015-03-02 Optimizing the use of biological therapy in patients with inflammatory bowel disease Moss, Alan C. Gastroenterol Rep (Oxf) Reviews Biological therapy revolutionized the treatment of inflammatory bowel disease (IBD) during the last decade. These monoclonal antibodies, which target tumor necrosis factor (TNF), integrins or IL12/23, have been approved—or are in development for—both Crohn’s disease (CD) and ulcerative colitis (UC). Early use of these agents taught clinicians that induction and maintenance therapy, coupled with immunomodulator agents, reduced the immunogenicity of these agents, and led to sustained remission in many patients. More recent data has demonstrated that, through dose adjustments, optimizing serum drug levels may also provide more durable maintenance of remission, and improved mucosal healing. This review examines clinical practices that may enhance clinical outcomes from biological therapy in IBD. Oxford University Press 2015-02 2015-01-06 /pmc/articles/PMC4324872/ /pubmed/25567472 http://dx.doi.org/10.1093/gastro/gou087 Text en © The Author(s) 2015. Published by Oxford University Press and the Digestive Science Publishing Co. Limited. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Moss, Alan C.
Optimizing the use of biological therapy in patients with inflammatory bowel disease
title Optimizing the use of biological therapy in patients with inflammatory bowel disease
title_full Optimizing the use of biological therapy in patients with inflammatory bowel disease
title_fullStr Optimizing the use of biological therapy in patients with inflammatory bowel disease
title_full_unstemmed Optimizing the use of biological therapy in patients with inflammatory bowel disease
title_short Optimizing the use of biological therapy in patients with inflammatory bowel disease
title_sort optimizing the use of biological therapy in patients with inflammatory bowel disease
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4324872/
https://www.ncbi.nlm.nih.gov/pubmed/25567472
http://dx.doi.org/10.1093/gastro/gou087
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