Neutralization of interleukin-17 aggravates dextran sulfate sodium-induced colitis in mice

被引:405
作者
Ogawa, A [1 ]
Andoh, A [1 ]
Araki, Y [1 ]
Bamba, T [1 ]
Fujiyama, Y [1 ]
机构
[1] Shiga Univ Med Sci, Dept Internal Med, Otsu, Shiga 5202192, Japan
关键词
cytokine; T cell; monocytes/macrophages;
D O I
10.1016/j.clim.2003.09.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We evaluated the effects of rat anti-mouse IL-17 neutralizing monoclonal antibody (mAb) on the development of dextran sulfate sodium (DSS)-induced colitis. Tissue samples were evaluated by standard immunohistochemical procedure. The mucosal mRNA expression of cytokines was analyzed by reverse transcriptase-polymerase chain reaction (RT-PCR). In the mice treated with the anti-IL-17 mAb, the body weight was significantly lower, and anal prolapse and colon shortening were apparent. A histological analysis indicated that the anti-IL-17 mAb markedly enhanced the severity of colitis. The mucosal infiltration of CD4-positive helper T cells and CD11b-positive granulocytes-monocytes was increased in the anti-IL-17 mAb-treated mice. Treatment with the anti-IL-17 mAb increased the mucosal expression of mRNAs of tumor necrosis factor (TNF)-alpha, interferon (IFN)-gamma, IL-6, RANTES, and IP-10. Blocking of IL-17 activity in vivo using the anti-IL-17 mAb enhanced the development of DSS-colitis in mice. This suggests an inhibitory role for IL-17 in the development of DSS-colitis. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:55 / 62
页数:8
相关论文
共 49 条
[1]  
Albanesi C, 1999, J IMMUNOL, V162, P494
[2]   IL-17 selectively down-regulates TNF-α-induced RANTES gene expression in human colonic subepithelial myofibroblasts [J].
Andoh, A ;
Fujino, S ;
Bamba, S ;
Araki, Y ;
Okuno, T ;
Bamba, T ;
Fujiyama, Y .
JOURNAL OF IMMUNOLOGY, 2002, 169 (04) :1683-1687
[3]   Mice with a selective deletion of the CC chemokine receptors 5 or 2 are protected from dextran sodium sulfate-mediated colitis:: Lack of CC chemokine receptor 5 expression results in a NK1.1+ lymphocyte-associated Th2-type immune response in the intestine [J].
Andres, PG ;
Beck, PL ;
Mizoguchi, E ;
Mizoguchi, A ;
Bhan, AK ;
Dawson, T ;
Kuziel, WA ;
Maeda, N ;
MacDermott, RP ;
Podolsky, DK ;
Reinecker, HC .
JOURNAL OF IMMUNOLOGY, 2000, 164 (12) :6303-6312
[4]   Blockade of interleukin 6 trans signaling suppresses T-cell resistance against apoptosis in chronic intestinal inflammation:: Evidence in Crohn disease and experimental colitis in vivo [J].
Atreya, R ;
Mudter, J ;
Finotto, S ;
Müllberg, J ;
Jostock, T ;
Wirtz, S ;
Schütz, M ;
Bartsch, B ;
Holtmann, M ;
Becker, C ;
Strand, D ;
Czaja, J ;
Schlaak, JF ;
Lehr, HA ;
Autschbach, F ;
Schürmann, G ;
Nishimoto, N ;
Yoshizaki, K ;
Ito, H ;
Kishimoto, T ;
Galle, PR ;
Rose-John, S ;
Neurath, MF .
NATURE MEDICINE, 2000, 6 (05) :583-588
[5]  
Awane M, 1999, J IMMUNOL, V162, P5337
[6]   Influence of immunogenicity on the long-term efficacy of infliximab in Crohn's disease [J].
Baert, F ;
Noman, M ;
Vermeire, S ;
Van Assche, G ;
D'Haens, G ;
Carbonez, A ;
Rutgeerts, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (07) :601-608
[7]   Role of endotoxin in intestinal reperfusion-induced expression of E-selectin [J].
Bauer, P ;
Russell, JM ;
Granger, DN .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1999, 276 (02) :G479-G484
[8]   Patients with inflammatory bowel disease (IBD) reveal increased induction capacity of intracellular interferon-gamma (IFN-γ) in peripheral CD8+ lymphocytes co-cultured with intestinal epithelial cells [J].
Bisping, G ;
Lügering, N ;
Lütke-Brintrup, S ;
Pauels, HG ;
Schürmann, G ;
Domschke, W ;
Kucharzik, T .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2001, 123 (01) :15-22
[9]   Lamina propria T cells in Crohn's disease and other gastrointestinal inflammation show defective CD2 pathway-induced apoptosis [J].
Boirivant, M ;
Marini, M ;
Di Felice, G ;
Pronio, AM ;
Montesani, C ;
Tersigni, R ;
Strober, W .
GASTROENTEROLOGY, 1999, 116 (03) :557-565
[10]  
Chabaud M, 1998, J IMMUNOL, V161, P409