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首页> 外文期刊>Clinical & translational oncology : >Antigen-loaded dendritic cells triggers a specific cytotoxic Tlymphocytes immune response against hepatocellular carcinoma: in vitro study
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Antigen-loaded dendritic cells triggers a specific cytotoxic Tlymphocytes immune response against hepatocellular carcinoma: in vitro study

机译:抗原的树突状细胞触发针对肝细胞癌的特异性细胞毒性Tlymphocytes免疫应答:体外研究

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BackgroundHepatocellular carcinoma (HCC) is one of the common malignancies, characterized by poor response to conventional therapeutic options. Immunotherapy with dendritic cells (DCs)-vaccines is one of the most successful strategies used for the treatment of HCC. However, the methods applied in the preparation of antigen-loaded DCs are important factors for optimization of DCs vaccines. PurposeThe present study was conducted to investigate the effect of HCC-whole tumor cell lysate prepared using rapid repetitive freeze-thaw cycles on the immunogenicity of DCs and evaluate the ability of whole tumor cell lysate-pulsed DCs vaccine to induce a specific cytotoxic Tlymphocytes (CTLs) response against HepG2 cell line. MethodsImmature DCs generated from peripheral blood monocytes were randomized into two groups: control DCs and whole tumor cell lysate-pulsed DCs. Phenotypic analysis of the DCs' cell maturation marker CD83 and co-stimulatory molecule CD86 was performed. HCC-specific cytotoxic activity of CD8(+) CTLs was measured in vitro.ResultsLoading of DCs with necrotic whole cell lysate resulted in non-significant changes in DCs' expression of CD83, but a significant increase in expression of CD86. In addition, CD8(+) CTLs stimulated with whole tumor cell lysate-pulsed DCs showed a high cytotoxic activity that specifically attack HepG2 cells.ConclusionOur findings indicated that pulsation of DCs with whole tumor cell lysate prepared by repetitive freeze-thaw cycles could efficiently enhance the ability of DCs to induce proliferation and clonal expansion of CD8(+) CTLs. Data herein, also indicated that whole tumor cell lysate-pulsed DCs triggers a specific CD8(+) CTLs against HCC tumor cells.
机译:BackgroundHepotocellular癌(HCC)是常见的恶性肿瘤之一,其特征在于对常规治疗选择的反应不良。用树突细胞(DCS)-Vaccines是用于治疗HCC的最成功的策略之一。然而,在制备抗原加载的DCS中施用的方法是用于优化DCS疫苗的重要因素。进行了目前的研究以研究使用快速重复冻融循环在DC的免疫原性制备的HCC-全肿瘤细胞裂解物的作用,并评估全肿瘤细胞裂解DCS疫苗诱导特异性细胞毒性TLYMPHOCYTES的能力(CTLS )对HepG2细胞系的反应。从外周血单核细胞产生的方法将来自外周血单核细胞的DC随机分为两组:对照DC和全肿瘤细胞裂解物脉冲DC。进行DCS细胞成熟标志物CD83和共刺激分子CD86的表型分析。在体外测量CD8(+)CTL的特异性细胞毒性活性。用坏死的全细胞裂解物进行DCS的Results载荷导致DCS表达的CD83表达的非显着变化,但CD86表达的显着增加。此外,用全肿瘤细胞裂解脉冲DC刺激的CD8(+)CTL显示出高细胞毒性活性,其特异性地发作HepG2细胞。结论调查结果表明,通过重复的冻融循环循环制备的全肿瘤细胞裂解物的DC脉动可以有效地增强DCS诱导CD8(+)CTL的增殖和克隆扩增的能力。本文的数据,还表明,整个肿瘤细胞裂解物脉冲DCS触发对HCC肿瘤细胞的特异性CD8(+)CTL。

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