Sobel D O, Newsome J
Division of Pediatric Endocrinology and Metabolism, Georgetown University Medical Center, Washington, D.C. 20007-2197, USA.
Clin Diagn Lab Immunol. 1997 Nov;4(6):764-8. doi: 10.1128/cdli.4.6.764-768.1997.
The BB rat model of human insulin-dependent diabetes mellitus (IDDM) spontaneously develops diabetes through an autoimmune process. Gamma interferon (IFN-gamma) is thought to play an important pathogenic role. This study examined if IFN-gamma administration can, paradoxically, prevent diabetes in BB rats. Diabetes-prone BB rats were initially injected intraperitoneally with murine recombinant IFN-gamma (rIFN-gamma) at doses of 0.5 x 10(4) to 40 x 10(4) U three times a week for 6 weeks beginning at 35 days of age. The effects of altering the duration of treatment (2 to 6 weeks) and the age at which injections were initiated (45 through 65 days) were also assessed. rIFN-gamma administration prevented the development of diabetes in a dose-dependent manner. The optimal treatment condition resulted in a 9.1% incidence of diabetes versus a 90% incidence in control rats. This diabetes-sparing effect was long lasting and continued to 7 months of age. A 4- to 6-week course resulted in maximal inhibition. Treatment initiated as late as 55 days of age, when insulitis is already present, was effective in preventing diabetes. Islet inflammation was dramatically lower in rIFN-gamma- versus saline-injected rats (P < 0.01). Total leukocyte count and subpopulations of peripheral mononuclear cells were unaltered by rIFN-gamma. In summary, rIFN-gamma paradoxically and potently prevents diabetes in BB rats in a dose-dependent fashion by inhibiting islet inflammation. This diabetes-sparing effect occurs even when injections are initiated after evidence of the diabetic process is already present.
人类胰岛素依赖型糖尿病(IDDM)的BB大鼠模型通过自身免疫过程自发发展为糖尿病。γ干扰素(IFN-γ)被认为起重要的致病作用。本研究检测了给予IFN-γ是否反而能预防BB大鼠患糖尿病。将易患糖尿病的BB大鼠在35日龄时开始,每周3次腹腔注射剂量为0.5×10⁴至40×10⁴U的鼠重组IFN-γ(rIFN-γ),持续6周。还评估了改变治疗持续时间(2至6周)和开始注射的年龄(45至65日龄)的影响。给予rIFN-γ以剂量依赖方式预防了糖尿病的发生。最佳治疗条件下糖尿病发病率为9.1%,而对照大鼠为90%。这种糖尿病保护作用持久,持续到7月龄。4至6周的疗程导致最大抑制。在55日龄(此时胰岛炎已存在)开始治疗有效预防了糖尿病。与注射生理盐水的大鼠相比,注射rIFN-γ的大鼠胰岛炎症显著减轻(P<0.01)。rIFN-γ未改变外周血白细胞总数和外周单个核细胞亚群。总之,rIFN-γ以剂量依赖方式反而有力地预防了BB大鼠患糖尿病,其机制是抑制胰岛炎症。即使在糖尿病过程已有证据后开始注射,这种糖尿病保护作用仍会出现。