文章摘要
何峰 肖宗慧 刘卓 肖萍 姚海兰 冯淼 刘哲伟.紫外灭活CVB3 病毒诱导BALB/c小鼠产生免疫保护作用的研究[J].,2016,16(20):3801-3805
紫外灭活CVB3 病毒诱导BALB/c小鼠产生免疫保护作用的研究
Study of Protective Immune Effect Induced by UV-inactivated CVB3 on the BALB/c Mice
  
DOI:
中文关键词: 紫外灭活型CVB3  细胞因子  中和抗体  免疫保护作用
英文关键词: UV-inactivated CVB3  Cytokines  Neutralizing antibody  Protective immune effect
基金项目:国家自然科学基金项目(81271809);北京市自然科学基金项目(7164241)
作者单位
何峰 肖宗慧 刘卓 肖萍 姚海兰 冯淼 刘哲伟 首都儿科研究所分子免疫室首都儿科研究所生化室首都儿科研究所附属儿童医院病理科 
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中文摘要:
      目的:探讨紫外灭活型CVB3 病毒诱导BALB/c 小鼠产生特异性免疫应答及保护作用的评估。方法:采用紫外灭活的方法处 理野生型CVB3 m株,按照0.1 LD50(104 PFU)的剂量免疫小鼠,设置PBS 免疫组作为对照,免疫后第3,5,7 天收集小鼠血清,检 测细胞因子含量;在第3,5,7,14 天分离小鼠脾脏,流式分析T 细胞亚群的分布比例;在免疫后一个月分离小鼠血清,检测中和抗 体的滴度;同时间给予小鼠100LD50 野生型CVB3 感染,观察小鼠的死亡率。结果:与对照组相比,在检测日期内紫外灭活型 CVB3 组小鼠血清中细胞因子IL-1alpha,TNF-alpha,IL-6 的表达量明显增高(P<0.05),IL-4 的表达量没有明显差异;免疫后第14 天 CD3+CD4+T细胞的分布较对照组明显升高(P<0.05);在免疫后一个月,紫外灭活型CVB3 免疫组可以诱导机体产生高滴度中和 抗体,同时,小鼠应对高致死量CVB3 感染时有较高的存活率。结论:紫外灭活型CVB3 感染能诱导机体产生特异性免疫应答,同 时,产生的中和抗体可以提高小鼠应对致死剂量CVB3 感染时的生存率,对机体有明显的保护作用。
英文摘要:
      Objective:To investigate specific immune response and protective effect of BALB/c mice induced by UV inactivated CVB3.Methods:Wild CVB3 mstrain was inactivated by UV, and male BALB/c mice were immunized with 0.1 LD50 (104 PFU) of UV inactivated CVB3, named CVB3-UV, PBS treated mice were set as compared group. On the 3, 5, 7 days post immunization mice were sacrificed, serum were collected and cytokines were detected by CBA method, T cell subset were analyzed by flow cytometry method in the splenocytes on the 3, 5, 7, 14 days post immunization, neutralizing antibody in the sera of immunized mice 1 month later were detected, further, mice survival rate were also evaluated after challenge with lethal dose of wild type CVB3.Results:Compared with PBS treated group, CVB3-UV could induce high levels of IL-1alpha, TNF-alpha and IL-6 (P<0.05), while IL-4 production was comparable between both groups. CD3+CD4+T cell development were found affected on the 14 days post immunization by CVB3-UV (P<0.05), and higher titer neutralizing antibody were induced in the CVB3-UV treated mice. Importantly, higher survival rate of mice were found in the CVB3-UV group after re-infection by lethal CVB3.Conclusion:UV-inactivated CVB3 could induce specific immune response and support obvious protective effect in BALB/c mice.
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