Novel targets for inflammatory bowel disease therapeutics.

Mark Löwenberg, Geert D'Haens
Author Information
  1. Mark Löwenberg: Department of Gastroenterology and Hepatology, Academic Medical Center, Amsterdam, The Netherlands. g.dhaens@amc.uva.nl

Abstract

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.

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MeSH Term

Adalimumab
Antibodies, Monoclonal
Antibodies, Monoclonal, Humanized
Cell Adhesion Molecules
Certolizumab Pegol
Colitis, Ulcerative
Crohn Disease
Humans
Immunoglobulin Fab Fragments
Infliximab
Natalizumab
Piperidines
Polyethylene Glycols
Protein Kinase Inhibitors
Pyrimidines
Pyrroles
Quinolones
Tumor Necrosis Factor-alpha
Ustekinumab

Chemicals

Antibodies, Monoclonal
Antibodies, Monoclonal, Humanized
Cell Adhesion Molecules
Immunoglobulin Fab Fragments
Natalizumab
Piperidines
Protein Kinase Inhibitors
Pyrimidines
Pyrroles
Quinolones
Tumor Necrosis Factor-alpha
Polyethylene Glycols
tofacitinib
laquinimod
golimumab
vedolizumab
Infliximab
Ustekinumab
Adalimumab
Certolizumab Pegol

Word Cloud

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