J Korean Ophthalmol Soc > Volume 48(8); 2007 > Article
Journal of the Korean Ophthalmological Society 2007;48(8):1143-1150.
DOI: https://doi.org/10.3341/jkos.2007.48.8.1143-1150    Published online August 31, 2007.
Therapeutic Effects of Anti-Tumor Necrosis Factor Monoclonal Antibody on Experimental Uveitis.
Eun Ryung Han, Min Jin Oh, Min Seon Cho, Ji Soo Lee, Jeong Hee Lee
1Department of Ophthalmology, School of Medicine, Ewha Womans University, Seoul, Korea. leejhoph@mm.ewha.ac.kr
2Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea.
3Department of Pathology, School of Medicine, Ewha Womans University Seoul, Korea.
4Department of Internal Medicine, School of Medicine, Ewha Womans University, Seoul, Korea.
실험적 포도막염에서 종양괴사인자 단일세포군항체의 치료 효과
한은령1,오민진2,조민선3,이지수4,이정희1
Department of Ophthalmology, School of Medicine, Ewha Womans University1, Seoul, Korea Department of Ophthalmology, Yonsei University College of Medicine2, Seoul, Korea Department of Pathology, School of Medicine, Ewha Womans University3 Seoul, Korea Department of Internal Medicine, School of Medicine, Ewha Womans University4, Seoul, Korea
Correspondence:  Jeong Hee Lee, M.D.
Abstract
PURPOSE
We investigated the therapeutic effects of monoclonal anti-TNF antibody (infliximab) on experimental uveitis. METHODS: Twenty New Zealand White rabbits were immunized with Mycobacterium tuberculosis H37Ra antigen and then challenged with intravitreal injection of tuberculin antigen to introduce a uveitis. Then infliximab was injected into rabbit eyes at an intravenous concentration of 5 mg/kg and intravitreal concentrations of 1 mg/0.1mL and 100 microg/0.1mL. As a control, the vehicle was injected intravenously or intravitreally. To evaluate the therapeutic effects, inflammation was assessed by slit lamp biomicroscopy and scored according to the severity of inflammation. The animals were also evaluated by electroretinography and histopathology. RESULTS: Regardless of the administration route, inflammatory activities of anterior chamber and engorgement of vascular structures were reduced in the infliximab treated group compared to control. Different administration routes and different concentrations of infliximab did not affect the therapeutic outcome of the clinical scoring. Intravenous (5 mg/kg) and intravitreal diluted (100 microg/0.1mL) infliximab injection groups showed significant improvement in electroretinographic findings and significant reduction of inflammatory cells with preservation of retinal tissue architecture on histopathologic examination. However, focal loss of the photoreceptor outer segment is observed in intravitreal undiluted (1 mg/0.1 mL) infliximab injected eyes. CONCLUSIONS: Infliximab may be a useful treatment modality to suppress ocular inflammation in experimental uveitis models in rabbits.
Key Words: Experimental uveitis;Infliximab;Tumor necrosis factor


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