Mechanisms behind efficacy of tumor necrosis factor inhibitors in inflammatory bowel diseases

被引:87
作者
Olesen, Caroline Meyer [1 ]
Coskun, Mehmet [1 ]
Peyrin-Biroulet, Laurent [2 ]
Nielsen, Ole Haagen [1 ]
机构
[1] Univ Copenhagen, Herlev Hosp, Dept Gastroenterol, Med Sect, DK-2730 Herlev, Denmark
[2] Lorraine Univ, Nancy Univ Hosp, Inserm U954, Dept Gastroenterol, Vandoeuvre Les Nancy, France
关键词
Crohn's disease; IBD; Inflammatory pathways; TNF inhibitors; Ulcerative colitis; INTERFERON-GAMMA PRODUCTION; ACTIVE ULCERATIVE-COLITIS; PROPRIA T-LYMPHOCYTES; ANTI-TNF TREATMENT; QUALITY-OF-LIFE; CROHNS-DISEASE; FACTOR-ALPHA; RHEUMATOID-ARTHRITIS; CERTOLIZUMAB PEGOL; INFLIXIMAB THERAPY;
D O I
10.1016/j.pharmthera.2016.01.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Biological treatment with tumor necrosis factor (TNF) inhibitors is successful in the management of inflammatory bowel disease (IBD). All TNF inhibitors antagonize the pro-inflammatory cytokine TNF-alpha but with varying efficacies in IBD. The variations in efficacy probably are caused by structural differences between the agents that affect their mechanisms of action and pharmacokinetic properties. Several mechanisms have been proposed, such as modulation of the expression of pro-inflammatory mediators and a reduction in the number of activated immune cells. However, it seems that clinical efficacy is the result of a number of different mechanisms and that binding of transmembrane TNF by TNF inhibitors. Knowledge of the mechanisms of action has been obtained mainly through the use of in vitro assays that may differ significantly from the situation in vivo. This review discusses the available data on TNF inhibitors in order to identify mechanisms of importance for their efficacy in IBD. Thus, a better understanding of the mechanistic basis for clinical efficacy can lead to a more rational use of TNF inhibitors in the management of IBD. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:110 / 119
页数:10
相关论文
共 117 条
[1]   Mucosal healing at 3 months predicts long-term endoscopic remission in anti-TNF-treated luminal Crohn's disease [J].
Af Bjorkesten, Clas-Goran ;
Nieminen, Urpo ;
Sipponen, Taina ;
Turunen, Ulla ;
Arkkila, Perttu ;
Farkkila, Martti .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2013, 48 (05) :543-551
[2]   Increased production of granulocyte-macrophage colony-stimulating factor in Crohn's disease - a possible target for infliximab treatment [J].
Agnholt, J ;
Kelsen, J ;
Brandsborg, B ;
Jakobsen, NO ;
Dahlerup, JF .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2004, 16 (07) :649-655
[3]   Infliximab downregulates interferon-γ production in activated gut T-lymphocytes from patients with Crohn's disease [J].
Agnholt, J ;
Kaltoft, K .
CYTOKINE, 2001, 15 (04) :212-222
[4]   Hepatocyte nuclear factor 4α in the intestinal epithelial cells protects against inflammatory bowel disease [J].
Ahn, Sung-Hoon ;
Shah, Yatrik M. ;
Inoue, Junko ;
Morimura, Keiichirou ;
Kim, Insook ;
Yim, SunHee ;
Lambert, Gilles ;
Kurotani, Reiko ;
Nagashima, Kunio ;
Gonzalez, Frank J. ;
Inoue, Yusuke .
INFLAMMATORY BOWEL DISEASES, 2008, 14 (07) :908-920
[5]   Mucosal Gene Expression of Cell Adhesion Molecules, Chemokines, and Chemokine Receptors in Patients With Inflammatory Bowel Disease Before and After Infliximab Treatment [J].
Arijs, Ingrid ;
De Hertogh, Gert ;
Machiels, Kathleen ;
Van Steen, Kristel ;
Lemaire, Katleen ;
Schraenen, Anica ;
Van Lommel, Leentje ;
Quintens, Roel ;
Van Assche, Gert ;
Vermeire, Severine ;
Schuit, Frans ;
Rutgeerts, Paul .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2011, 106 (04) :748-761
[6]   ANTI-TNF AGENTS AS THERAPEUTIC CHOICE IN IMMUNE-MEDIATED INFLAMMATORY DISEASES: FOCUS ON ADALIMUMAB [J].
Armuzzi, A. ;
Lionetti, P. ;
Blandizzi, C. ;
Caporali, R. ;
Chimenti, S. ;
Cimino, L. ;
Gionchetti, P. ;
Girolomoni, G. ;
Lapadula, G. ;
Marchesoni, A. ;
Marcellusi, A. ;
Mennini, F. S. ;
Salvarani, C. ;
Cimaz, R. .
INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2014, 27 :11-32
[7]   Differences in binding and effector functions between classes of TNF antagonists [J].
Arora, Taruna ;
Padaki, Rupa ;
Liu, Ling ;
Hamburger, Agnes E. ;
Ellison, Aaron R. ;
Stevens, Seth R. ;
Louie, James S. ;
Kohno, Tadahiko .
CYTOKINE, 2009, 45 (02) :124-131
[8]   Antibodies Against Tumor Necrosis Factor (TNF) Induce T-Cell Apoptosis in Patients With Inflammatory Bowel Diseases via TNF Receptor 2 and Intestinal CD14+ Macrophages [J].
Atreya, Raja ;
Zimmer, Michael ;
Bartsch, Brigitte ;
Waldner, Maximilian J. ;
Atreya, Imke ;
Neumann, Helmut ;
Hildner, Kai ;
Hoffman, Arthur ;
Kiesslich, Ralf ;
Rink, Andreas D. ;
Rau, Tilman T. ;
Rose-John, Stefan ;
Kessler, Hermann ;
Schmidt, Jan ;
Neurath, Markus F. .
GASTROENTEROLOGY, 2011, 141 (06) :2026-2038
[9]   LIPOPOLYSACCHARIDE-INDUCED INTERLEUKIN-10 IN MICE - ROLE OF ENDOGENOUS TUMOR-NECROSIS-FACTOR-ALPHA [J].
BARSIG, J ;
KUSTERS, S ;
VOGT, K ;
VOLK, HD ;
TIEGS, G ;
WENDEL, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (10) :2888-2893
[10]  
Benucci Maurizio, 2012, Acta Biomed, V83, P72