Tobe T, Takahashi K, Ohkuma H, Uyama M
Department of Ophthalmology, Kansai Medical University, Osaka-fu, Japan.
Nippon Ganka Gakkai Zasshi. 1995 May;99(5):571-81.
We studied histologically the effect of systemic administration of human interferon-beta (IFN-beta) on experimental choroidal neovascularization which was caused by intensive laser photocoagulation at the posterior pole of monkey eyes. The regression of choroidal neovascularization was observed in IFN-treated monkeys. Histologically, retinal pigment epithelium (RPE) was remarkably abundant around choroidal neovascularization in the subretinal space, and the activity of neovascularization was weaker in IFN-treated monkeys than in untreated monkeys. These results indicate that IFN-beta promotes the proliferation of RPE and suppresses the activity of endothelial cells of neovascularization to cause regression of choroidal neovascularization. The results suggest that IFN-beta is clinically useful to treat the choroidal neovascularization of age-related macular degeneration.
我们通过组织学方法研究了全身给予人β-干扰素(IFN-β)对实验性脉络膜新生血管形成的影响,该实验性脉络膜新生血管形成是由对猴眼后极部进行高强度激光光凝引起的。在接受IFN治疗的猴子中观察到脉络膜新生血管的消退。组织学上,视网膜色素上皮(RPE)在视网膜下间隙的脉络膜新生血管周围明显丰富,并且与未治疗的猴子相比,接受IFN治疗的猴子中新生血管形成的活性较弱。这些结果表明,IFN-β促进RPE的增殖并抑制新生血管内皮细胞的活性,从而导致脉络膜新生血管消退。结果提示,IFN-β在临床上可用于治疗年龄相关性黄斑变性的脉络膜新生血管。