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:CAR-NK cell therapy: latest updates from the 2024 ASH annual meeting.
CAR-NK cell therapy: latest updates from the 2024 ASH annual meeting.
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NK 细胞是固有免疫应答的重要组成部分,具有无需预先暴露即可识别并清除癌细胞的固有能力,使其成为免疫治疗策略的理想候选。嵌合抗原受体工程化自然杀伤(CAR-NK)细胞无需人类白细胞抗原配型,简化了个体化方案并促进了现货型产品的制造。此外,CAR-NK细胞疗法发生细胞因子释放综合征和神经毒性的风险较低,使患者获益于更高的安全性。然而,CAR-NK细胞疗法同样面临挑战,包括但不限于寿命短和肿瘤微环境的限制。在此,我们总结了2024年ASH年会上CAR-NK细胞疗法临床前研究和临床试验的最新进展。
Natural killer cells, integral to the innate immune response, exhibit the inherent capacity to identify and eliminate cancer cells without prior exposure, positioning them as prime candidates for immunotherapeutic strategies. Chimeric antigen receptor-engineered natural killer (CAR-NK) cells obviate the requirement for human leukocyte antigen compatibility, simplifying personalized schedules and facilitating the manufacture of off-the-shelf products.
In addition, CAR-NK cell therapy possesses lower risk of cytokine release syndrome and neurotoxicity, benefitting patients with higher security. Nevertheless, CAR-NK cell therapy is also confronted with challenges, including but not limited to short lifespan and restrictions from tumor microenvironment.
Here, we summarized the latest advancements in the preclinical investigations and clinical trials of CAR-NK cell therapy from the 2024 ASH Annual Meeting.
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