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Emerging treatments for inflammatory bowel disease

Inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), is characterized by chronic inflammation, a relapsing and remitting clinical course, requirement for lifelong medication and often, significant morbidity. While multiple effective therapeutic options exist...

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Detalles Bibliográficos
Autores principales: Hazel, Karl, O’Connor, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003169/
https://www.ncbi.nlm.nih.gov/pubmed/32076497
http://dx.doi.org/10.1177/2040622319899297
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author Hazel, Karl
O’Connor, Anthony
author_facet Hazel, Karl
O’Connor, Anthony
author_sort Hazel, Karl
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description Inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), is characterized by chronic inflammation, a relapsing and remitting clinical course, requirement for lifelong medication and often, significant morbidity. While multiple effective therapeutic options exist for the treatment of IBD, a proportion of patients will either fail to respond or lose response to therapy. Advances in therapeutics, such as the gut-specific anti-integrins, now offer patients an alternative option to systemic immunosuppression. Anti-interleukin 12 (anti-IL-12)/IL-23 agents offer new and effective treatment options for CD, while the oral small molecules now offer an oral alternative for the treatment of moderate-to-severe disease, previously requiring subcutaneous injection or intravenous infusion. Alternatives to pharmacological treatment such as stem-cell transplant and faecal microbiota transplant are also showing some promise in the treatment of both CD and UC.
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spelling pubmed-70031692020-02-19 Emerging treatments for inflammatory bowel disease Hazel, Karl O’Connor, Anthony Ther Adv Chronic Dis Review Inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), is characterized by chronic inflammation, a relapsing and remitting clinical course, requirement for lifelong medication and often, significant morbidity. While multiple effective therapeutic options exist for the treatment of IBD, a proportion of patients will either fail to respond or lose response to therapy. Advances in therapeutics, such as the gut-specific anti-integrins, now offer patients an alternative option to systemic immunosuppression. Anti-interleukin 12 (anti-IL-12)/IL-23 agents offer new and effective treatment options for CD, while the oral small molecules now offer an oral alternative for the treatment of moderate-to-severe disease, previously requiring subcutaneous injection or intravenous infusion. Alternatives to pharmacological treatment such as stem-cell transplant and faecal microbiota transplant are also showing some promise in the treatment of both CD and UC. SAGE Publications 2020-02-05 /pmc/articles/PMC7003169/ /pubmed/32076497 http://dx.doi.org/10.1177/2040622319899297 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
Hazel, Karl
O’Connor, Anthony
Emerging treatments for inflammatory bowel disease
title Emerging treatments for inflammatory bowel disease
title_full Emerging treatments for inflammatory bowel disease
title_fullStr Emerging treatments for inflammatory bowel disease
title_full_unstemmed Emerging treatments for inflammatory bowel disease
title_short Emerging treatments for inflammatory bowel disease
title_sort emerging treatments for inflammatory bowel disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003169/
https://www.ncbi.nlm.nih.gov/pubmed/32076497
http://dx.doi.org/10.1177/2040622319899297
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