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热休克蛋白融合蛋白抗肿瘤免疫佐剂的初步筛选

陈亚静1,吴秀丽2,王 丽1,卫红飞2,王丽颖2,于永利 1   

  1. 1.吉林大学基础医学院免疫学教研室,吉林 长春 130021;2.吉林大学基础医学院分子生物学教研室,吉林 长春 130021)
  • 收稿日期:2006-12-19 修回日期:1900-01-01 出版日期:2007-07-28 发布日期:2007-07-28
  • 通讯作者: 于永利

Primary screening of antitumor immunoadjuvants combined with heat shock fusion protein

CHEN Ya-jing1,WU Xiu-li2,WANG Li1,WEI Hong-fei2,WANG Li-ying2,YU Yong-li1   

  1. (1.Department of Immunology,School of Basic Medical Sciences,Jilin University,Changchun 130021,China; 2.Department of Molecular Biology,School of Basic Medical Sciences,Jilin University,Changchun 130021,China)
  • Received:2006-12-19 Revised:1900-01-01 Online:2007-07-28 Published:2007-07-28
  • Contact: YU Yong-li

摘要: 目的:筛选一种具有增强热休克融合蛋白HSP-MUC1抗肿瘤作用的免疫佐剂。方法:将HSP-MUC1与新型CpG ODN或人源性IFNα2b混合后皮下注射MUC1阳性荷瘤小鼠,各分4组,分别是磷酸盐缓冲液(PBS)、HSP-MUC1、CpG ODN(hIFNα2b)及HSP-MUC1+CpG ODN(HSP-MUC1+hIFNα 2b)。观察各组肿瘤发生率及肿瘤体积变化。结果:HSP-MUC1+CpG ODN组与PBS组及HSP-MUC1组比较小鼠的肿瘤发生率及肿瘤重量均降低(P<0.05);单独应用CpG ODN组表现出与HSP-MUC1+CpG ODN组相似的抑瘤作用,与PBS组及HSP-MUC1组比较,肿瘤发生率及肿瘤的重量均降低(P<0.05);而HSP-MUC1+IFNα2b组与PBS组及HSP-MUC1组比较,小鼠肿瘤发生率及肿瘤重量差异均无显著性(P>0.05)。结论:CpG ODN是一种能增强HSP-MUC10抗肿瘤作用的免疫佐剂,人源性IFNα2b则不能增强HSP-MUC1的抗肿瘤活性。

关键词: HSP-MUC1, CpG ODN, 干扰素 , 疫苗, 合成, 佐剂, 免疫

Abstract: To screen one kind of antitumor immunoadjuvant that could enhance the anti-tumor activity of heat shock fusion protein(HSP-MUC1).Methods MUC1-positive tumor bearing mice were subcutaneously injected by HSP-MUC1 combined with a novel CpG ODN or hIFNα2b,four groups were set up respectively as PBS,HSP-MUC1,CpG ODN(IFNα2b) and HSP-MUC1+CpG ODN(HSP-MUC1+IFNα2b).The tumor incidence and tumor volume in various groups were observed and calculated. Results The tumor incidence and tumor weight of mice in HSP-MUC1+CpG ODN group were lower than those in PBS group and HSP-MUC1 group(P<0.05); CpG ODN alone also displayed the similar anti-tumor effect as HSP-MUC1+CpG ODN,it could decrease the tumor incidence and tumor weight of mice compared with PBS and HSP-MUC1(P<0.05); And the tumor incidence and tumor weight of mice in HSP-MUC1+hIFNα2b group had no difference with those in PBS group and HSP-MUC1 group(P> 0.05). Conclusion CpG ODN could enhance the anti-tumor activity of HSP-MUC1 but need to be further determined for its optimal injection time;and human IFNα2b could not enhance the anti-tumor activity of HSP-MUC1.

Key words: HSP-MUC1, CpG ODN, interferon-alpha, vaccine, synthetic, adjuvant, immunologic

中图分类号: 

  • R979.1