Novel targets for inflammatory bowel disease therapeutics

被引:30
|
作者
Löwenberg M. [1 ]
D'Haens G. [1 ,2 ,3 ]
机构
[1] Department of Gastroenterology and Hepatology, Academic Medical Center, Amsterdam
[2] Clinical Trials, European Division, Amsterdam
[3] Department of Gastroenterology, Meibergdreef 9
关键词
Adhesion molecule blockers; Anti-tumor necrosis factor (TNF) antibodies; Biologicals; Crohn's disease (CD); Inflammatory bowel disease (IBD); Small molecules; Tofacitinib; Ulcerative colitis (UC); Ustekinumab; Vedolizumab;
D O I
10.1007/s11894-012-0311-3
中图分类号
学科分类号
摘要
In recent years, many new agents have been evaluated for the treatment of inflammatory bowel disease. In this paper, we critically review recently published literature about these novel therapies, which have been the result of extensive research identifying molecular targets. Of the various biologicals and small molecules that have recently been tested in clinical trials, several demonstrated clinical efficacy with a tolerable safety profile. We discuss a number of them with specific focus on vedolizumab, a monoclonal antibody directed against the alpha4beta7 integrin on lymphocytes, ustekinumab, a monoclonal antibody against the p40 subunit of interleukin-12 and interleukin-23, and tofacitinib, a small molecule targeting Janus-activated kinase. Most likely, these three agents will find their way to the market and offer significant therapeutic alternatives for the management of Crohn's disease and/or ulcerative colitis. © 2013 Springer Science+Business Media New York.
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