Designing biologic selectivity for inflammatory bowel disease – role of vedolizumab
Niklas Krupka, Daniel C Baumgart Division of Gastroenterology and Hepatology, Department of Medicine, Charité Medical School, Humboldt-University of Berlin, Berlin, Germany Abstract: Crohn’s disease and ulcerative colitis are two chronic inflammatory bowel conditions. Current...
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2014-12-01
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doaj-c0a16c9f53414a9f855d7693aaa4e2662020-11-24T23:23:01ZengDove Medical PressDrug Design, Development and Therapy1177-88812014-12-012015default14715419638Designing biologic selectivity for inflammatory bowel disease – role of vedolizumabKrupka NBaumgart DC Niklas Krupka, Daniel C Baumgart Division of Gastroenterology and Hepatology, Department of Medicine, Charité Medical School, Humboldt-University of Berlin, Berlin, Germany Abstract: Crohn’s disease and ulcerative colitis are two chronic inflammatory bowel conditions. Current approved biologic therapies are limited to blocking tumor necrosis factor alpha. Unfortunately, some patients are primary nonresponders, experiencing a loss of response, intolerance, or side effects. This defines an unmet need for novel therapeutic strategies. The rapid recruitment and inappropriate retention of leukocytes is a hallmark of chronic inflammation and a potentially promising therapeutic target. Here we discuss the clinical trial results of vedolizumab (anti-α4β7, LDP-02, MLN-02, and MLN0002) and its impact on future management of inflammatory bowel disease. Keywords: ulcerative colitis, Crohn’s disease, vedolizumab, MLN0002, MLN-02, LDP-02, anti-α4β7http://www.dovepress.com/designing-biologic-selectivity-for-inflammatory-bowel-disease-ndash-ro-peer-reviewed-article-DDDT |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Krupka N Baumgart DC |
spellingShingle |
Krupka N Baumgart DC Designing biologic selectivity for inflammatory bowel disease – role of vedolizumab Drug Design, Development and Therapy |
author_facet |
Krupka N Baumgart DC |
author_sort |
Krupka N |
title |
Designing biologic selectivity for inflammatory bowel disease – role of vedolizumab |
title_short |
Designing biologic selectivity for inflammatory bowel disease – role of vedolizumab |
title_full |
Designing biologic selectivity for inflammatory bowel disease – role of vedolizumab |
title_fullStr |
Designing biologic selectivity for inflammatory bowel disease – role of vedolizumab |
title_full_unstemmed |
Designing biologic selectivity for inflammatory bowel disease – role of vedolizumab |
title_sort |
designing biologic selectivity for inflammatory bowel disease – role of vedolizumab |
publisher |
Dove Medical Press |
series |
Drug Design, Development and Therapy |
issn |
1177-8881 |
publishDate |
2014-12-01 |
description |
Niklas Krupka, Daniel C Baumgart Division of Gastroenterology and Hepatology, Department of Medicine, Charité Medical School, Humboldt-University of Berlin, Berlin, Germany Abstract: Crohn’s disease and ulcerative colitis are two chronic inflammatory bowel conditions. Current approved biologic therapies are limited to blocking tumor necrosis factor alpha. Unfortunately, some patients are primary nonresponders, experiencing a loss of response, intolerance, or side effects. This defines an unmet need for novel therapeutic strategies. The rapid recruitment and inappropriate retention of leukocytes is a hallmark of chronic inflammation and a potentially promising therapeutic target. Here we discuss the clinical trial results of vedolizumab (anti-α4β7, LDP-02, MLN-02, and MLN0002) and its impact on future management of inflammatory bowel disease. Keywords: ulcerative colitis, Crohn’s disease, vedolizumab, MLN0002, MLN-02, LDP-02, anti-α4β7 |
url |
http://www.dovepress.com/designing-biologic-selectivity-for-inflammatory-bowel-disease-ndash-ro-peer-reviewed-article-DDDT |
work_keys_str_mv |
AT krupkan designingbiologicselectivityforinflammatoryboweldiseasendashroleofvedolizumab AT baumgartdc designingbiologicselectivityforinflammatoryboweldiseasendashroleofvedolizumab |
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