Emerging Therapies for Inflammatory Bowel Diseases

被引:2
作者
Khanna, Reena [1 ,3 ]
Feagan, Brian G. [1 ,2 ,3 ]
机构
[1] Univ Western Ontario, Dept Med, London, ON, Canada
[2] Univ Western Ontario, Dept Biostat & Epidemiol, London, ON, Canada
[3] Robarts Clin Trials Inc, Robarts Res Inst, London, ON, Canada
关键词
Inflammatory bowel disease; Interleukin inhibitors; Janus kinase inhibitors; SMAD; 7; Vedolizumab; EARLY COMBINED IMMUNOSUPPRESSION; MULTICENTER DOUBLE-BLIND; ANTIBODY PF-00547659 PF; JANUS KINASE INHIBITOR; CROHNS-DISEASE; MAINTENANCE THERAPY; ULCERATIVE-COLITIS; INDUCTION THERAPY; VEDOLIZUMAB; MODERATE;
D O I
10.1159/000447378
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: The past decade has seen important advances in the management of chronic inflammatory bowel diseases (IBD), consisting of Crohn's disease (CD) and ulcerative colitis. The development of TNF antagonists, the recognition of interrupting lymphocyte trafficking as an effective treatment strategy, confirmation of the value of combination therapy, and the need, particularly in CD, for the treatment of high-risk patients early in the disease course are all fundamental concepts upon which the next generation of IBD treatment algorithms will be built. Emerging concepts that will continue to evolve and shape the field include an increased emphasis on personalized medicine (right drug, right dose, right time) and the development of new therapeutic classes. In this article, we review the clinical data and provide some insights into recent data regarding IBD therapies. Key Messages: In this article, we review the mechanism of action and data for novel therapies in IBD with particular focus on the evidence for agents targeting leukocyte trafficking, cytokine signaling, including interleukin12/23 and the Janus kinasesignal transducers/activators of transcription pathway, and the emergence of antisense therapy for the treatment of IBD. Conclusions: Multiple new therapies are emerging for IBD; however, the potential positioning of these agents in treatment algorithms is difficult to predict in the absence of comparative effectiveness studies. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:67 / 73
页数:7
相关论文
共 35 条
[1]   MECHANISMS OF DISEASE Inflammatory Bowel Disease [J].
Abraham, Clara ;
Cho, Judy H. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (21) :2066-2078
[2]  
[Anonymous], 2016, PFIZ ANN POS TOP LIN
[3]   ALPHA-4-BETA-7-INTEGRIN MEDIATES LYMPHOCYTE BINDING TO THE MUCOSAL VASCULAR ADDRESSIN MADCAM-1 [J].
BERLIN, C ;
BERG, EL ;
BRISKIN, MJ ;
ANDREW, DP ;
KILSHAW, PJ ;
HOLZMANN, B ;
WEISSMAN, IL ;
HAMANN, A ;
BUTCHER, EC .
CELL, 1993, 74 (01) :185-195
[4]   Proinflammatory cytokines disrupt epithelial barrier function by apoptosis-independent mechanisms [J].
Bruewer, M ;
Luegering, A ;
Kucharzik, T ;
Parkos, CA ;
Madara, JL ;
Hopkins, AM ;
Nusrat, A .
JOURNAL OF IMMUNOLOGY, 2003, 171 (11) :6164-6172
[5]  
CEPEK KL, 1993, J IMMUNOL, V150, P3459
[6]   Evolving medical therapies for ulcerative colitis. [J].
Cohen R.D. .
Current Gastroenterology Reports, 2002, 4 (6) :497-505
[7]  
D'Haens G, 2015, J CROHNS COLITIS, V9, pS14
[8]   Early combined immunosuppression or conventional management in patients with newly diagnosed Crohn's disease:: an open randomised trial [J].
D'Haens, Geert ;
Baert, Filip ;
van Assche, Gert ;
Caenepeel, Philip ;
Vergauwe, Philippe ;
Tuynman, Hans ;
De Vos, Martine ;
van Deventer, Sander ;
Stitt, Larry ;
Donner, Allan ;
Vermeire, Severine ;
Van De Mierop, Frank J. ;
Coche, Jean-Charles R. ;
van der Woude, Janneke ;
Ochsenkuehn, Thomas ;
van Bodegraven, Ad A. ;
van Hootegem, Philippe P. ;
Lambrecht, Guy L. ;
Mana, Fazia ;
Rutgeerts, Paul ;
Feagan, Brian G. ;
Hommes, Daniel .
LANCET, 2008, 371 (9613) :660-667
[9]   Interleukin-23: A key cytokine in inflammatory diseases [J].
Duvallet, Emilie ;
Semerano, Luca ;
Assier, Eric ;
Falgarone, Geraldine ;
Boissier, Marie-Christophe .
ANNALS OF MEDICINE, 2011, 43 (07) :503-511
[10]   Development of small-molecule inhibitors of sphingosine-1-phosphate signaling [J].
Edmonds, Yvette ;
Milstien, Sheldon ;
Spiegel, Sarah .
PHARMACOLOGY & THERAPEUTICS, 2011, 132 (03) :352-360