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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Main Authors: Krupka N, Baumgart DC
Format: Article
Language:English
Published: Dove Medical Press 2014-12-01
Series:Drug Design, Development and Therapy
Online Access:http://www.dovepress.com/designing-biologic-selectivity-for-inflammatory-bowel-disease-ndash-ro-peer-reviewed-article-DDDT
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spelling 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
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