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作 者:吴先闯[1] 林海红[1] 杜钢军[1] 杨义明[2] 姬利延[1] 卢琳琳[1] 于丽娟[1] 尚跃军[2] 周霖[2]
机构地区:[1]河南大学药学院药理教研室,河南开封475004 [2]开封市第二人民医院内科,河南开封475001
出 处:《河南大学学报(医学版)》2009年第3期174-177,共4页Journal of Henan University:Medical Science
基 金:河南省科技攻关项目(632030200);开封市科技攻关项目(080344-46)
摘 要:目的:观察灯盏花素对肿瘤诱导的小鼠免疫抑制的影响。方法:小鼠脾脏细胞体外培养观察灯盏花素对淋巴细胞增殖和淋巴细胞因子分泌的的影响;lewis肺癌荷瘤小鼠迟发型变态反应、血清淋巴细胞因子水平及CD8+T细胞对lewis肺癌的细胞毒作用检测灯盏花素对小鼠免疫抑制的逆转作用。结果:灯盏花素体外对刀豆蛋白(ConA)诱导的小鼠脾脏细胞增殖有增强作用,能抑制转化生长因子β1(TGF-β1)和白细胞介素4(IL-4),促进的干扰素λ(IFN-λ)和白细胞介素2(IL-2)。体内灯盏花素能逆转荷瘤小鼠迟发型变态反应、血清淋巴细胞因子水平及CD8+T细胞对lewis肺癌的无能作用,并一定程度抑制肿瘤生长。结论:灯盏花素作为TGF-β1抑制剂对肿瘤诱导的小鼠免疫抑制有逆转作用。Objective: To observe effects of breviscapine tumor induced immunosuppression by breviscapine in mice. Methods: The effects of breviscapine on lymphocyte proliferation and cytokines secretion were examined by cultured spleen cells in vitro. The reversal of tumor induced immunosuppression was assessed by delayed type hypersensitivity, lymphocyte factors level and CD8+cytotoxicity against lewis lung cancer cells in mice bearing lewis lung cancer. Results: In vitro, breviscapine could enhance lymphocyte proliferation induced by ConA, inhibit TGF-β1and IL-4 , promote IFN-λ, and IL 2. In vivo, breviscapine could reverse delayed type hypersensitivity, lymphocyte factors level and CD8+T cell anergy against lewis lung cancer cells in mice bearing lewis lung cancer. Conclusion: Breviscapine as a TGF-β1 inhibitor could reverse tumor-induced immunosuppression in mice.
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