Effects of the immunomodulator, VGX-1027, in endotoxin-induced uveitis in Lewis rats

被引:8
|
作者
Mangano, K. [1 ]
Sardesai, N. Y. [2 ]
Quattrocchi, C. [1 ]
Mazzon, E. [3 ]
Cuzzocrea, S. [3 ]
Bendtzen, K. [4 ]
Meroni, P. L. [5 ]
Kim, J. J. [2 ]
Nicoletti, F. [1 ]
机构
[1] Univ Catania, Dept Biomed Sci, I-95124 Catania, Italy
[2] VGX Pharmaceut, Blue Bell, PA USA
[3] Policlin Univ, Dept Clin & Expt Med & Pharmacol, Messina, Italy
[4] Natl Univ Hosp, Rigshosp, Inst Inflammat Res, Copenhagen, Denmark
[5] Univ Milan, IRCCS Inst Auxol Italiano, Allergy Clin Immunol & Rheumatol Unit, Dept Internal Med, Milan, Italy
关键词
cytokines; immunotherapy; uveitis; VGX-1027;
D O I
10.1038/bjp.2008.315
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and purpose: VGX-1027 is a novel, low molecular weight, immunomodulatory compound that has shown efficacy against a variety of immuno-inflammatory disease models in animals including autoimmune diabetes in NOD mice, collagen-induced arthritis and chemically induced inflammatory colitis. Here, we have studied the effects of VGX-1027 on the development of endotoxin-induced uveitis (EIU) in male Lewis rats, as a model of inflammatory ocular diseases in humans. Experimental approach: EIU was induced by a single footpad injection of 200 mu g lipopolysaccharide (LPS). Groups of rats were treated with either VGX-1027 (25 mg kg(-1)) or its vehicle at different time points (30 min, 6 h or 12 h) after the challenge with LPS or, as positive control, with dexamethasone. The rats were killed within 16 h after LPS challenge, and the eyes and aqueous humor were collected to study serological, immunological and histological signs of EIU. Key results: The rats treated with VGX-1027 within 6 h after LPS challenge exhibited milder clinical, histological and laboratory signs of EIU than those treated with vehicle. Conclusion and implications: This study provides the first evidence that systemic treatment with VGX-1027 counteracts the uveitis-inducing effect of LPS in rats and suggests that this drug may have potential in the treatment of immuno-inflammatory conditions of the eye in humans.
引用
收藏
页码:722 / 730
页数:9
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