Ogata Toshiyuki, Yamazaki Hideya, Teshima Teruki, Tsuchiya Takahiro, Nishimoto Norihiro, Matsuura Nariaki
Departments of Radiation Oncology.
Exp Ther Med. 2012 Aug;4(2):273-276. doi: 10.3892/etm.2012.582. Epub 2012 May 18.
We previously showed that early administration of monoclonal anti-interleukin-6 receptor antibody (IL-6RA) does not prevent radiation-induced lung injury in mice. The purpose of this study was to investigate whether a higher dose and longer course of IL-6RA treatment was effective in ameliorating radiation pneumonia. C57Bl/6J mice received thoracic irradiation of 12 Gy, and were intraperitoneally injected with the IL-6RA, namely MR16-1, or with control rat IgG 4 times, once immediately following exposure and then weekly from 1 to 3 weeks after irradiation. Enzyme-linked immunosorbent assays were used to analyze the plasma levels of IL-6 and serum amyloid A (SAA). Lung injury was assessed by histological staining with haematoxylin and eosin (H&E) and by measuring wet lung weight. We observed marked upregulation of IL-6 in IL-6RA-treated mice compared to the IgG-treated control group, whereas IL-6RA did not increase the production of SAA in the group receiving irradiation. However, radiation pneumonia, as evaluated by H&E staining and lung weight showed no differences between the IL-6RA-treated mice and the controls. Long-term treatment with high-dose IL-6RA does not ameliorate radiation pneumonia.
我们之前表明,早期给予单克隆抗白细胞介素-6受体抗体(IL-6RA)并不能预防小鼠辐射诱导的肺损伤。本研究的目的是调查更高剂量和更长疗程的IL-6RA治疗是否能有效改善放射性肺炎。C57Bl/6J小鼠接受12 Gy的胸部照射,并腹腔注射IL-6RA(即MR16-1)或对照大鼠IgG 4次,一次在照射后立即注射,然后在照射后1至3周每周注射一次。采用酶联免疫吸附测定法分析血浆IL-6和血清淀粉样蛋白A(SAA)水平。通过苏木精和伊红(H&E)组织学染色以及测量肺湿重评估肺损伤。与IgG治疗的对照组相比,我们观察到IL-6RA治疗的小鼠中IL-6明显上调,而IL-6RA在接受照射的组中并未增加SAA的产生。然而,通过H&E染色和肺重量评估的放射性肺炎在IL-6RA治疗的小鼠和对照组之间没有差异。高剂量IL-6RA的长期治疗并不能改善放射性肺炎。