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Application of genetically engineered Salmonella typhimurium for interferon-gamma-induced therapy against melanoma

机译:转基因沙门氏菌毒蕈酮对混合物瘤的干扰素 - γ诱导治疗的应用

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Salmonella have been experimentally used as anti-cancer agents, because they show selective growth in tumours. In this study, we genetically modified attenuated Salmonella typhimurium to express and secrete interferon-gammS. typhimurium or S. typhimurium expressing empty vector (S. typhimurium [Vec]) in a natural killer (NK) cell-dependent manner. Moreover, genetically modified Salmonella, including S. typhimurium (IFN-gamma), showed little toxicity to normal tissues with no observable adverse effects. However, S. typhimurium (IFN-gamma)-mediated tumour suppression was attributed to direct killing of tumour cells rather than to stable anti-tumour immunity. Collectively, these results suggest that tumour-targeted therapy using S. typhimurium (IFN-gamma) has potential for melanoma treatment. (C) 2016 Elsevier Ltd. All rights reserved.a (IFN-gamma) as a tumouricidal agent to enhance the therapeutic efficacy of Salmonella. IFN-gamma was fused to the N-terminal region (residues 1e160) of SipB (SipB160) for secretion from bacterial cells. Attenuated S. typhimurium expressing recombinant IFN-gamma (S. typhimurium (IFN-gamma)) invaded the melanoma cells and induced cytotoxicity. Subcutaneous administration of S. typhimurium (IFN-gamma) also efficiently inhibited tumour growth and prolonged the survival of C57BL/6 mice bearing B16F10 melanoma compared with administration of phosphate-buffered saline (PBS), unmodified S. typhimurium or S. typhimurium expressing empty vector (S. typhimurium [Vec]) in a natural killer (NK) cell-dependent manner. Moreover, genetically modified Salmonella, including S. typhimurium (IFN-gamma), showed little toxicity to normal tissues with no observable adverse effects. However, S. typhimurium (IFN-gamma)-mediated tumour suppression was attributed to direct killing of tumour cells rather than to stable anti-tumour immunity. Collectively, these results suggest that tumour-targeted therapy using S. typhimurium (IFN-gamma) has potential for melanoma treatment. (C) 2016 Elsevier Ltd. All rights reserved.
机译:沙门氏菌已经通过实验用作抗癌剂,因为它们表现出肿瘤的选择性生长。在这项研究中,我们遗传修饰减毒的毒蕈氏菌毒蕈,以表达和分泌干扰素-GAMM。在天然杀伤者(NK)细胞依赖方式中表达伤寒毒蕈或S. Typhimurium表达空的载体(S. typhimurium [Vec])。此外,遗传修饰的沙门氏菌,包括S. typhimurium(IFN-Gamma),对正常组织表现出几乎没有可观察的不良反应的毒性。然而,S.Typhimurium(IFN-Gamma)介导的肿瘤抑制归因于直接杀死肿瘤细胞,而不是稳定的抗肿瘤免疫。总的来说,这些结果表明,使用S.鼠李毒蕈(IFN-Gamma)的肿瘤靶向治疗具有黑素瘤治疗的可能性。 (c)2016 Elsevier Ltd.保留所有权利。(IFN-Gamma)作为巨大毒性药剂,以增强沙门氏菌的治疗效果。 IFN-GAMMA与SIPB(SIPB160)的N-末端区域(残基1E160)融合,用于从细菌细胞分泌。减毒的S.表达重组IFN-Gamma(S.Typhimurium(IFN-Gamma))侵入黑素瘤细胞并诱导细胞毒性。皮下施用S.培丘硫脲(IFN-Gamma)也有效地抑制肿瘤生长,延长了含有B16F10黑色素瘤的C57BL / 6小鼠的存活,与磷酸盐缓冲盐水(PBS),未修饰的S. Typhimurium或S.表达空的伤寒伤前度载体(S. typhimurium [Vec])以天然杀伤(NK)细胞依赖性方式。此外,遗传修饰的沙门氏菌,包括S. typhimurium(IFN-Gamma),对正常组织表现出几乎没有可观察的不良反应的毒性。然而,S.Typhimurium(IFN-Gamma)介导的肿瘤抑制归因于直接杀死肿瘤细胞,而不是稳定的抗肿瘤免疫。总的来说,这些结果表明,使用S.鼠李毒蕈(IFN-Gamma)的肿瘤靶向治疗具有黑素瘤治疗的可能性。 (c)2016 Elsevier Ltd.保留所有权利。

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