Literature DB >> 20134493

Future biologic targets for IBD: potentials and pitfalls.

Gil Y Melmed1, Stephan R Targan.   

Abstract

The treatment of patients with IBD has evolved towards biologic therapy, which seeks to target specific immune and biochemical abnormalities at the molecular and cellular level. Multiple genes have been associated with susceptibility to IBD, and many of these can be linked to alterations in immune pathways. These immune pathways provide avenues for understanding the pathogenesis of IBD and suggest future drug targets, such as the IL-12-IL-23 pathway. In addition, failed therapeutic drug trials can provide valuable information about pitfalls in study design, drug delivery and disease activity assessment. Future biologic drug development will benefit from the early identification of subsets of patients who are most likely to respond to therapy by use of biological markers of genetic susceptibility or immunologic susceptibility.

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Year:  2010        PMID: 20134493     DOI: 10.1038/nrgastro.2009.218

Source DB:  PubMed          Journal:  Nat Rev Gastroenterol Hepatol        ISSN: 1759-5045            Impact factor:   46.802


  86 in total

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7.  G protein-coupled receptor kinase-2-deficient mice are protected from dextran sodium sulfate-induced acute colitis.

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8.  Genetic variants synthesize to produce paneth cell phenotypes that define subtypes of Crohn's disease.

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10.  Dietary grape seed extract ameliorates symptoms of inflammatory bowel disease in IL10-deficient mice.

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