Current and emerging therapeutic targets for IBD

被引:462
|
作者
Neurath, Markus F. [1 ]
机构
[1] Univ Erlangen Nurnberg, Ludwig Demling Endoscopy Ctr Excellence, Dept Med 1, Kussmaul Campus Med Res,Ulmenweg 18, D-91054 Erlangen, Germany
关键词
INFLAMMATORY BOWEL DISEASES; ACTIVE CROHNS-DISEASE; TUMOR-NECROSIS-FACTOR; EARLY COMBINED IMMUNOSUPPRESSION; CHRONIC INTESTINAL INFLAMMATION; JANUS KINASE INHIBITOR; MESENCHYMAL STEM-CELLS; INNATE LYMPHOID-CELLS; GROWTH-FACTOR-BETA; MAINTENANCE THERAPY;
D O I
10.1038/nrgastro.2016.208
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Various therapeutic advances have led to a paradigm shift in the clinical management of patients with IBD. The introduction of immunosuppressive (such as azathioprine) and biologic agents (such as TNF blockers) has markedly reduced the need to use corticosteroids for therapy. Furthermore, the alpha 4 beta 7 integrin blocker vedolizumab has been introduced for clinical IBD therapy. Moreover, various new inhibitors of cytokines (for example, IL-6-IL-6R and IL-12-IL-23 blockers or apremilast), modulators of cytokine signalling events (for example, JAK inhibitors or SMAD7 blocker), inhibitors of transcription factors (for example, GATA3 or ROR gamma t) and new anti-adhesion and anti-T-cell-activation and migration strategies (for example, beta 7 integrin, sphingosine 1-phosphate receptors and MAdCAM1 inhibitors, regulatory T-cell therapy and stem cells) arecurrently being evaluated in controlled clinical trials. This Review aims to provide a comprehensive overview about current and future therapeutic approaches for IBD therapy. Furthermore, potential mechanisms of action of these therapeutic approaches and their implications for clinical therapy in IBD are discussed.
引用
收藏
页码:269 / 278
页数:10
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