Anscher Mitchell S, Thrasher Bradley, Rabbani Zahid, Teicher Beverly, Vujaskovic Zeljko
Department of Radiation Oncology, Duke University Medical Center, Durham, NC, USA.
Int J Radiat Oncol Biol Phys. 2006 Jul 1;65(3):876-81. doi: 10.1016/j.ijrobp.2006.02.051.
The aim of this study was to determine whether a neutralizing transforming growth factor-beta (TGFbeta) antibody can prevent radiation (RT) induced lung injury.
Fractionated and sham right lung irradiation in Fischer 344 rats was delivered to assess the radioprotective effect of the antibodies. Animals were divided into the following groups: (1) control (sham RT, control antibody 13C4); (2) RT (800cGy x 5)+13C4); (3) RT + 0.1 mg/kg 1D11 anti-TGFbeta antibody; and (4) RT + 1 mg/kg 1D11 antibody. Antibodies were intraperitoneally administered immediately after the last fraction of RT. Animals were sacrificed at 6 and 26 weeks after irradiation. Lungs were assessed for histologic changes, activation of macrophages, expression/activation of TGFbeta and its signal transduction pathway.
At 6 weeks post-RT, there was a significant reduction in macrophage accumulation (p = 0.041), alveolar wall thickness (p = 0.0003), and TGF-beta activation (p = 0.032) in animals receiving 1.0 mg/kg 1D11 vs. in the control group. However, at 6 weeks, the low dose of 1D11 antibody (0.1 mg/kg) failed to produce any significant changes. At 6 months post-RT, radioprotection is apparent for the group receiving 1.0 mg/kg 1D11, with activated macrophages (p = 0.037), alveolar wall thickness (p = 0.0002), TGFbeta activation (p = 0.002) and its signal transduction proteins (p < 0.05) compared with the control group.
Administration of a single dose of 1.0 mg/kg of the anti-TGFbeta antibody 1D11 resulted in decreased morphologic changes, inflammatory response, and reduced expression and activation of TGFbeta 6 weeks and 6 months after 40 Gy to the right hemithorax. Targeting the TGFbeta pathway may be a useful strategy to prevent radiation-induced lung injury.
本研究旨在确定一种中和转化生长因子-β(TGFβ)抗体是否能预防辐射(RT)诱导的肺损伤。
对Fischer 344大鼠进行分次右肺照射和假照射,以评估抗体的辐射防护效果。动物分为以下几组:(1)对照组(假RT,对照抗体13C4);(2)RT(800cGy×5)+13C4);(3)RT + 0.1mg/kg 1D11抗TGFβ抗体;(4)RT + 1mg/kg 1D11抗体。在最后一次RT照射后立即腹腔注射抗体。在照射后6周和26周处死动物。评估肺组织的组织学变化、巨噬细胞活化、TGFβ及其信号转导途径的表达/活化情况。
在RT后6周,接受1.0mg/kg 1D11的动物与对照组相比,巨噬细胞积聚(p = 0.041)、肺泡壁厚度(p = 0.0003)和TGF-β活化(p = 0.032)显著降低。然而,在6周时,低剂量的1D11抗体(0.1mg/kg)未产生任何显著变化。在RT后6个月,接受1.0mg/kg 1D11的组显示出明显的辐射防护作用,与对照组相比,巨噬细胞活化(p = 0.037)、肺泡壁厚度(p = 0.0002)、TGFβ活化(p = 0.002)及其信号转导蛋白(p < 0.05)均有改善。
单次给予1.0mg/kg抗TGFβ抗体1D11可减少右半胸接受40Gy照射后6周和6个月时的形态学变化、炎症反应,并降低TGFβ的表达和活化。靶向TGFβ途径可能是预防辐射诱导肺损伤的有效策略。