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Enhanced antitumoral efficacy by intratumoral perfusion of activated macrophages associated with photodynamic therapy

机译:通过与光动力疗法相关的活化巨噬细胞的肠灌注增强了抗肿瘤效果

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Experiments were performed on five batches of Wistar inbred rats with Walker-256 carcinosarcoma receiving photodynamic therapy (PDT), rMuIFN-gamma activated macrophages (AM$Phi@) or associated therapy (PDT-AM$Phi@-A; PDT-AM$Phi@-B); the control batch (HBSS) consisted of animals with untreated Walker-256 tumors. The results were as follows: the sole treatment (PDT, AM$Phi@) gave survival rates between 57.2 and 57.7% and cure rates ranging from 23.1 to 34.3%. The 'combined' therapy in multiple doses increased significantly (87.9%) the survival rate of tumor bearing rats as well as the rate of complete tumor regression (72.7%). Cell-mediated immunity test values in batches III and IV exposed to multiple doses of PDT-AM$Phi showed higher values as compared to the values noticed in batches I -II and the control batch V, performed at 12 and 21 days post-treatment. Summing up, these results demonstrate that 'combined' photodynamic treatment and biotherapy with interferon activated macrophages stimulate cell-mediated antitumoral activity, increase survival rates and reduce incidence of Walker-256 carcinosarcoma in rat model.
机译:对五批Wistar近交大鼠进行实验,伴随着Walker-256癌癌接受光动力治疗(PDT),RMUIFN-Gamma活化巨噬细胞(AM $ PHI @)或相关治疗(PDT-AM $ PHI @ -A; PDT-AM $ PHI @ -b);对照批次(HBSS)由具有未处理的Walker-256肿瘤的动物组成。结果如下:唯一的治疗(PDT,AM $ @)在57.2和57.7%之间产生的存活率,治愈率范围为23.1至34.3%。多剂量的“组合”治疗显着增加(87.9%)肿瘤轴承大鼠的存活率以及完全肿瘤回归速度(72.7%)。与批次I-II和对照分批v的值相比,细胞介导的批次III和IV的批量抗药性检测值显示为多剂量的PDT-AM $ PHI,并且在治疗后12天和21天进行的对照分批V. 。总结,这些结果表明,“组合”光动力处理和与干扰素活化巨噬细胞的生物治疗刺激细胞介导的抗肿瘤活性,提高存活率,减少大鼠模型中的步行者-256癌癌的发病率。

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