RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Decorin-armed oncolytic adenovirus promotes natural killers (NKs) activation and infiltration to enhance NK therapy in CRC model.
Decorin-armed oncolytic adenovirus promotes natural killers (NKs) activation and infiltration to enhance NK therapy in CRC model.
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结直肠癌(CRC)是常见的胃肠道恶性肿瘤;2020年其全球发病率和死亡率分别居第三位和第二位。近年来免疫治疗发展迅速。NK细胞无需受主要组织相容性复合体限制即可识别并杀伤肿瘤细胞,因此在肿瘤免疫治疗领域日益受到关注。
然而,肿瘤微环境中的限制因素会阻碍NK细胞浸润和增殖,导致NK细胞疗法治疗实体瘤的疗效不佳。溶瘤病毒疗法具有免疫原性,有望增强抗肿瘤免疫反应并促进免疫细胞浸润。
本研究在异种移植小鼠模型中,将NK细胞与携带Decorin的溶瘤腺病毒(rAd.DCN)联合,用于治疗CRC。通过流式细胞术、实时定量PCR和Calcein-AM释放实验,我们发现rAd.DCN可有效促进NK细胞增殖、活化和脱颗粒,上调与NK细胞杀伤活性相关因子的表达和分泌,并增强其杀伤能力;其效果优于空载对照溶瘤病毒rAd.Null。联合治疗显著抑制肿瘤生长,增加外周血NK细胞数量,增强NK细胞杀伤功能,并提高穿孔素和IFN-γ表达水平。
同时,更多NK细胞被招募并浸润肿瘤组织。本研究证实了NK细胞与溶瘤腺病毒联合应用的可行性,从而拓展了NK细胞用于CRC潜在治愈性治疗的范围。
Colorectal cancer (CRC) is a prevalent malignant tumor of the gastrointestinal system, with the third and second highest incidence and mortality rates globally in 2020, respectively. Immunotherapy has developed rapidly in recent years. Natural killer (NK) cells have received increasing attention in the field of tumor immunotherapy due to their recognition and killing tumor cells without the limitations of major histocompatibility complexes.
However, constraints within the tumor microenvironment that impede the infiltration and proliferation of NK cells result in poor efficacy of NK cell therapy for solid tumors. Oncolytic viral therapy is an immunogenic treatment with the potential to enhance anti-tumour immune responses and promote immune cell infiltration. In this study, we synergistically combine NK cells with an oncolytic adenovirus carrying Decorin (rAd. DCN) for the treatment of colorectal cancer (CRC) in a xenograft mouse model. By using Flow cytometry, real-time quantitative PCR and Calcein-AM release assay, we found that rAd.
DCN could effectively promote proliferation, activation and degranulation of NK cells, up-regulate expression and secretion of NK cell killing activity-related factors, and enhance their killing activity. The efficacy is better than that of the blank control oncolytic virus rAd. Null.
Combined treatment significantly inhibited tumor growth, increased the number of NK cells in peripheral blood, promoted the killing function of NK cells, and increased the expression levels of perforin and IFN- . At the same time, more NK cells were recruited to infiltrate tumor tissue.
Our study established the feasibility of combination NK cells and oncolytic adenovirus application, thus expanding the scope of potentially curative treatments for NK cells in CRC.
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