Interleukin-1 and Tumor Necrosis Factor-Alpha: Novel Targets for Immunotherapy in Eales Disease

被引:10
作者
Saxena, Sandeep [1 ]
Pant, Aditya B. [2 ]
Khanna, Vinay K. [2 ]
Agarwal, A. K. [2 ]
Singh, Kamlesh [3 ]
Kumar, Dipak [1 ]
Singh, Vijay K. [4 ]
机构
[1] King Georges Med Univ, Dept Ophthalmol, Lucknow 226003, Uttar Pradesh, India
[2] Ind Toxicol Res Ctr, Lucknow 226001, Uttar Pradesh, India
[3] King Georges Med Univ, KGMC Inst Clin Epidemiol, Lucknow, Uttar Pradesh, India
[4] Armed Forces Radiobiol Res Inst, Radiat Counter Measures Program, Bethesda, MD USA
关键词
cytokines; Eales disease; interleukin; tumor necrosis factor; S-ANTIGEN; UVEITIS; INDUCTION; MICE;
D O I
10.1080/09273940902731015
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background: Eales disease is an idiopathic obliterative vasculopathy that primarily affects the peripheral retina of young adults. The authors evaluated interleukin 1 beta (IL-1), interleukin-6 (IL-6), Interleukin-10 (IL-10), and tumor necrosis factor-alpha (TNF-) in the serum of patients with Eales disease stages for the first time. Methods: The study group consisted of 45 consecutive patients of Eales disease [inflammatory stage (n = 15) and proliferative stage (n = 30)] and 28 healthy controls. Immunoassays for the quantification of the levels of four cytokines including IL-1, IL-6, IL-10, and TNF- in the serum samples were performed using ELISA kits. Results: IL-1, IL-6, IL-10, and TNF- levels were found to be increased significantly in the inflammatory stage of Eales disease as compared to controls (p .001). IL-1 levels decreased significantly during the proliferative stage of the disease as compared to the inflammatory stage (p = .03). TNF- levels increased significantly during the proliferative stage as compared to the inflammatory stage (p = .02). Conclusions: Raised levels of IL-1 and TNF- were observed in the inflammatory stage and persisted in the proliferative stage of the disease. The IL-1 system and TNF- represent novel target for immunotherapy for controlling inflammatory activity and/or the associated long-term sequelae related to angiogenesis in Eales disease.
引用
收藏
页码:201 / 206
页数:6
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