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首页> 外文期刊>Journal for ImmunoTherapy of Cancer >CCL5-armed oncolytic virus augments CCR5-engineered NK cell infiltration and antitumor efficiency
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CCL5-armed oncolytic virus augments CCR5-engineered NK cell infiltration and antitumor efficiency

机译:CCL5武装氯霉素增强CCR5工程的NK细胞渗透和抗肿瘤效率

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Background Natural killer (NK) cells have potent antitumor activities. Nevertheless, adoptive transfer therapy of NK cells has gained very limited success in patients with solid tumors as most infused NK cells remain circulating in the peripheral blood instead of entering tumor sites. Chemokines and their receptors play important roles in NK cell distribution. Enhancing chemokine receptors on immune cells to match and be driven to tumor-specific chemokines may improve the therapeutic efficacy of NK cells. Methods The CCR5-CCL5 axis is critical in NK cell homing to tumor sites. Thus, we analyzed CCR5 expression on NK cells from patients with cancer and healthy donors. We then upregulated CCR5 and CCL5 with lentiviruses and oncolytic viruses in NK and tumor cells, respectively. Animal experiments were also carried out to test the efficacy of the combination of oncolytic virus with NK cells. Results In NK cells from patients with various solid tumors or healthy subjects, CCR5 was expressed at low levels before and after expansion in vitro. CCR5-engineered NK cells showed enhanced tumor infiltration and antitumor effects, but no complete regressions were noted in the in vivo tumor models. To further improve therapeutic efficacy, we constructed CCL5-expressing oncolytic vaccinia virus. In vitro data demonstrated that vaccinia virus can produce CCL5 in tumor cells while infectivity remained unaffected. Supernatants from tumor cells infected by CCL5-modified vaccinia virus enhanced the directional movement of CCR5-overexpressed NK cells but not green fluorescent protein (GFP)-expressing cells. More importantly, NK cells were resistant to the vaccinia virus and their functions were not affected after being in contact. In vivo assays demonstrated that CCL5-expressing vaccinia virus induced a greater accumulation of NK cells within tumor lesions compared with that of the prototype virus. Conclusion Enhancement of matched chemokines and chemokine receptors is a promising method of increasing NK cell homing and therapeutic effects. Oncolytic vaccinia viruses that express specific chemokines can synergistically augment the efficacies of NK cell-based therapy.
机译:背景自然杀伤(NK)细胞具有有效的抗肿瘤活动。尽管如此,由于大多数注入的NK细胞在外周血中循环而不是进入肿瘤部位而不是进入肿瘤部位,因此,NK细胞的养老患者的养老疗法已经获得了非常有限的成功。趋化因子及其受体在NK细胞分布中发挥着重要作用。增强免疫细胞上的趋化因子受体匹配并被驱动到肿瘤特异性趋化因子,可以改善NK细胞的治疗效果。方法CCR5-CCL5轴在NK细胞归巢中至关重要。因此,我们分析了来自癌症和健康供体患者的NK细胞上的CCR5表达。然后,我们将CCR5和CCL5与Lentiviruses和NK和肿瘤细胞中的氯化物病毒上调。还进行了动物实验,以测试糖尿病病毒与NK细胞的组合的功效。结果来自各种实体肿瘤或健康受试者的患者的NK细胞,CCR5在体外膨胀之前和之后的低水平表达。 CCR5工程的NK细胞显示出增强的肿瘤渗透和抗肿瘤效应,但在体内肿瘤模型中没有注意到完全回归。为了进一步提高治疗效果,我们构建了CCL5表达溶血性痘苗病毒。体外数据表明,痘苗病毒可以在肿瘤细胞中产生CCl5,而感染性仍然不受影响。来自CCL5改性的疫苗病毒感染的肿瘤细胞的上清液增强了CCR5过表达NK细胞的定向运动,但不是绿色荧光蛋白(GFP) - 抑制细胞。更重要的是,NK细胞对痘苗病毒耐药性,并且在接触后,它们的功能不会受到影响。在体内测定中表明,与原型病毒相比,CCL5表达疫苗病毒在肿瘤病变中诱导NK细胞的较大积累。结论匹配趋化因子和趋化因子受体的增强是增加NK细胞归巢和治疗效果的有希望的方法。表达特定趋化因子的溶氯痘毒性病毒可以协同增强基于NK细胞的治疗的疗效。

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