Damianovich Maya, Blank Miri, Raiter Anat, Hardy Britta, Shoenfeld Yehuda
Department of Medicine B, Center for Autoimmune Diseases, Sheba Medical Center, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Hashomer, Israel.
Int Immunol. 2009 Sep;21(9):1057-63. doi: 10.1093/intimm/dxp070. Epub 2009 Jul 22.
Intravenous immunoglobulins (IVIg) preparations can be beneficial therapeutic agents for the treatment of tumor metastases as has been shown in both human and animal studies. Operating mechanisms have not yet been completely elucidated. Some of the mechanisms proposed entail the stimulation of the production of IL-12, a cytokine that exhibits anti-angiogenic activities, as well as inhibition of endothelial cells proliferation and vascular endothelial growth factor (VEGF) secretion. The aim of the present study was to investigate whether in an IVIg preparation there are natural antibodies directed against VEGF with the potential to affect angiogenesis. Using both sandwich and direct ELISA assays, IVIg was found to specifically recognize and bind VEGF in a dose-dependent manner. The binding specificity was confirmed by inhibition of IVIg binding to VEGF by VEGF as an inhibitor, as shown by ELISA and immunoblot. A mouse hind limb ischemia model was employed to evaluate the in vivo IVIg-induced inhibition of angiogenesis. IVIg was found to exhibit inhibitory effect on VEGF-mediated blood perfusion in the ischemic limb. The present study shows a presence of anti-VEGF fraction in IVIg preparation.
静脉注射免疫球蛋白(IVIg)制剂可能是治疗肿瘤转移的有益治疗药物,这在人体和动物研究中均已得到证实。其作用机制尚未完全阐明。提出的一些机制包括刺激白细胞介素-12(IL-12)的产生,IL-12是一种具有抗血管生成活性的细胞因子,同时还能抑制内皮细胞增殖和血管内皮生长因子(VEGF)分泌。本研究的目的是调查IVIg制剂中是否存在针对VEGF的天然抗体,这些抗体可能影响血管生成。使用夹心ELISA和直接ELISA检测方法,发现IVIg能够以剂量依赖的方式特异性识别并结合VEGF。通过ELISA和免疫印迹显示,VEGF作为抑制剂可抑制IVIg与VEGF的结合,从而证实了结合特异性。采用小鼠后肢缺血模型评估IVIg在体内对血管生成的抑制作用。发现IVIg对缺血肢体中VEGF介导的血液灌注具有抑制作用。本研究表明IVIg制剂中存在抗VEGF组分。