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抗白细胞介素-6受体抗体不能改善小鼠放射性肺炎。

Anti-IL-6 receptor antibody does not ameliorate radiation pneumonia in mice.

作者信息

Ogata Toshiyuki, Yamazaki Hideya, Teshima Teruki, Tsuchiya Takahiro, Nishimoto Norihiro, Matsuura Nariaki

机构信息

Departments of Radiation Oncology.

出版信息

Exp Ther Med. 2012 Aug;4(2):273-276. doi: 10.3892/etm.2012.582. Epub 2012 May 18.

Abstract

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.

摘要

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。

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