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Reovirus-Mediated Cytotoxicity and Enhancement of Innate Immune Responses Against Acute Myeloid Leukemia

机译:呼肠孤病毒介导的细胞毒性和针对急性髓性白血病的先天免疫反应的增强。

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Reovirus is a naturally occurring oncolytic virus that has shown preclinical efficacy in the treatment of a wide range of tumor types and has now reached phase III testing in clinical trials. The anti-cancer activity of reovirus has been attributed to both its direct oncolytic activity and the enhancement of anti-tumor immune responses. In this study, we have investigated the direct effect of reovirus on acute myeloid leukemia (AML) cells and its potential to enhance innate immune responses against AML, including the testing of primary samples from patients. Reovirus was found to replicate in and kill AML cell lines, and to reduce cell viability in primary AML samples. The pro-inflammatory cytokine interferon alpha (IFNα) and the chemokine (C-C motif) ligand 5 (known as RANTES [regulated upon activation, normal T-cell expressed, and secreted]) were also secreted from AML cells in response to virus treatment. In addition, reovirus-mediated activation of natural killer (NK) cells, within the context of peripheral blood mononuclear cells, stimulated their anti-leukemia response, with increased NK degranulation and IFNγ production and enhanced killing of AML targets. These data suggest that reovirus has the potential as both a direct cytotoxic and an immunotherapeutic agent for the treatment of AML.
机译:呼肠孤病毒是一种天然存在的溶瘤病毒,已显示出可治疗多种肿瘤的临床前功效,现已进入临床试验的III期测试。呼肠孤病毒的抗癌活性已归因于其直接溶瘤活性和抗肿瘤免疫应答的增强。在这项研究中,我们研究了呼肠孤病毒对急性髓细胞白血病(AML)细胞的直接作用及其增强针对AML的固有免疫应答的潜力,包括测试患者的主要样本。发现呼肠孤病毒可在AML细胞系中复制并杀死它们,并降低原发性AML样品中的细胞活力。响应病毒治疗,AML细胞也分泌促炎性细胞因子干扰素α(IFNα)和趋化因子(C-C基序)配体5(称为RANTES [在激活时受调节,正常T细胞表达和分泌])。另外,在外周血单核细胞的背景下,呼肠孤病毒介导的自然杀伤(NK)细胞活化激活了其抗白血病反应,并增加了NK脱粒和IFNγ的产生,并增强了对AML目标的杀伤力。这些数据表明,呼肠孤病毒具有作为直接细胞毒性和免疫治疗剂治疗AML的潜力。

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