Novel Targeted Therapies for Inflammatory Bowel Disease

被引:149
作者
Coskun, Mehmet [1 ,2 ,3 ]
Vermeire, Severine [4 ]
Nielsen, Ole Haagen [1 ]
机构
[1] Univ Copenhagen, Herlev Hosp, Med Sect, Dept Gastroenterol, Copenhagen, Denmark
[2] Univ Copenhagen, Dept Biol, Bioinformat Ctr, Copenhagen, Denmark
[3] Univ Copenhagen, BRIC, Copenhagen, Denmark
[4] Univ Hosp Gasthuisberg, Dept Gastroenterol, Leuven, Belgium
关键词
SEVERE CROHNS-DISEASE; SMAD7 ANTISENSE OLIGONUCLEOTIDE; NECROSIS-FACTOR INHIBITORS; ACTIVE ULCERATIVE-COLITIS; JANUS KINASE INHIBITOR; INDUCTION THERAPY; MAINTENANCE THERAPY; MONOCLONAL-ANTIBODY; DOUBLE-BLIND; ENDOTHELIAL-CELLS;
D O I
10.1016/j.tips.2016.10.014
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Our growing understanding of the immunopathogenesis of inflammatory bowel disease (IBD) has opened new avenues for developing targeted therapies. These advances in treatment options targeting different mechanisms of action offer new hope for personalized management. In this review we highlight emerging novel and easily administered therapeutics that may be viable candidates for the management of IBD, such as antibodies against interleukin 6 (IL-6) and IL-12/23, small molecules including Janus kinase inhibitors, antisense oligonucleotide against SMAD7 mRNA, and inhibitors of leukocyte trafficking to intestinal sites of inflammation (e.g., sphingosine 1-phosphate receptor modulators). We also provide an update on the current status in clinical development of these new classes of therapeutics.
引用
收藏
页码:127 / 142
页数:16
相关论文
共 102 条
[1]
Atale-Kachole P., 2014, J CLIN PATHOL, V67, P932
[2]
Molecular pathways controlling barrier function in IBD [J].
Atreya, Raja ;
Neurath, Markus F. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2015, 12 (02) :67-68
[3]
Crohn's disease [J].
Baumgart, Daniel C. ;
Sandborn, William J. .
LANCET, 2012, 380 (9853) :1590-1605
[4]
Enhanced leukocyte binding by intestinal microvascular endothelial cells in inflammatory bowel disease [J].
Binion, DG ;
West, GA ;
Ina, K ;
Ziats, NP ;
Emancipator, SN ;
Fiocchi, C .
GASTROENTEROLOGY, 1997, 112 (06) :1895-1907
[5]
Risk of Natalizumab-Associated Progressive Multifocal Leukoencephalopathy [J].
Bloomgren, Gary ;
Richman, Sandra ;
Hotermans, Christophe ;
Subramanyam, Meena ;
Goelz, Susan ;
Natarajan, Amy ;
Lee, Sophia ;
Plavina, Tatiana ;
Scanlon, James V. ;
Sandrock, Alfred ;
Bozic, Carmen .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (20) :1870-1880
[6]
The new orally active immunoregulator laquinimod (ABR-215062) effectively inhibits development and relapses of experimental autoimmune encephomyelitis [J].
Brunmark, C ;
Runström, A ;
Ohlsson, L ;
Sparre, B ;
Brodin, T ;
Åström, M ;
Hedlund, G .
JOURNAL OF NEUROIMMUNOLOGY, 2002, 130 (1-2) :163-172
[7]
The burden of inflammatory bowel disease in Europe [J].
Burisch, Johan ;
Jess, Tine ;
Martinato, Matteo ;
Lakatos, Peter L. .
JOURNAL OF CROHNS & COLITIS, 2013, 7 (04) :322-337
[8]
Fibrogenesis in Crohn's disease [J].
Burke, John P. ;
Mulsow, Jurgen J. ;
O'Keane, Conor ;
Docherty, Neil G. ;
Watson, R. William G. ;
O'Connell, P. Ronan .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2007, 102 (02) :439-448
[9]
IL-6 biology: implications for clinical targeting in rheumatic disease [J].
Calabrese, Leonard H. ;
Rose-John, Stefan .
NATURE REVIEWS RHEUMATOLOGY, 2014, 10 (12) :720-727
[10]
The involvement of gut microbiota in inflammatory bowel disease pathogenesis: Potential for therapy [J].
Cammarota, Giovanni ;
Ianiro, Gianluca ;
Cianci, Rossella ;
Sibbo, Stefano ;
Gasbarrini, Antonio ;
Curro, Diego .
PHARMACOLOGY & THERAPEUTICS, 2015, 149 :191-212