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:NK Cell-Based Immunotherapy in Colorectal Cancer.
NK Cell-Based Immunotherapy in Colorectal Cancer.
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人类自然杀伤(NK)细胞是免疫中的全能选手,因为它们能对转化细胞作出强大而即时的反应,并具有调节随后适应性免疫应答的能力。基于NK细胞参与的免疫疗法潜力最初在血液系统肿瘤中得以揭示,但也启发了针对实体瘤(包括结直肠癌(CRC))设计不同的免疫工具。事实上,尽管有癌症预防筛查计划、手术和化疗策略,CRC仍是最广泛传播且死亡率最高的癌症之一。因此,迫切需要进一步有效且互补的免疫基础疗法。在这篇综述中,我们汇集了旨在对抗CRC的基于NK细胞的免疫疗法的最新进展,特别是使用靶向肿瘤相关抗原(TAA)的单克隆抗体、免疫检查点阻断,以及过继性NK细胞疗法,包括用嵌合抗原受体修饰的NK细胞(CAR-NK)。
Human Natural Killer (NK) cells are all round players in immunity thanks to their powerful and immediate response against transformed cells and the ability to modulate the subsequent adaptive immune response.
The potential of immunotherapies based on NK cell involvement has been initially revealed in the hematological setting but has inspired the design of different immune tools to also be applied against solid tumors, including colorectal cancer (CRC). Indeed, despite cancer prevention screening plans, surgery, and chemotherapy strategies, CRC is one of the most widespread cancers and with the highest mortality rate.
Therefore, further efficient and complementary immune-based therapies are in urgent need. In this review, we gathered the most recent advances in NK cell-based immunotherapies aimed at fighting CRC, in particular, the use of monoclonal antibodies targeting tumor-associated antigens (TAAs), immune checkpoint blockade, and adoptive NK cell therapy, including NK cells modified with chimeric antigen receptor (CAR-NK).
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