Targeting IL-23 and Th17-cytokines in inflammatory bowel diseases.

Abstract:

:Over the last 15 years, the use of various biological therapies has largely improved the way we manage patients with Inflammatory Bowel Diseases (IBDs). Blockade of cytokine synthesis and/or activity is at the forefront of this new era with the success of inhibitors of tumor necrosis factor (TNF)-α. These therapies are however not effective in all IBD patients and efficacy may wane. Moreover, patients treated with anti-TNF-α antibodies can develop severe side-effects and new immune-mediated diseases. Therefore, a new challenge is to elucidate new inflammatory networks in the IBD tissue and develop novel anti-cytokine compounds, which may act in patients who are resistant to or cannot receive anti-TNF-α therapies. In this article we review the available data supporting the pathogenic role of IL-23 and Th17-related cytokines in IBD, and discuss whether and how compounds that control the activity of these cytokines may enter into the therapeutic armamentarium of IBD.

journal_name

Curr Pharm Des

authors

De Nitto D,Sarra M,Cupi ML,Pallone F,Monteleone G

doi

10.2174/138161210794079164

subject

Has Abstract

pub_date

2010-01-01 00:00:00

pages

3656-60

issue

33

eissn

1381-6128

issn

1873-4286

pii

BSP/CPD/E-Pub/000268

journal_volume

16

pub_type

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