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:Harnessing the Power of NK Cell Receptor Engineering as a New Prospect in Cancer Immunotherapy.
Harnessing the Power of NK Cell Receptor Engineering as a New Prospect in Cancer Immunotherapy.
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自然杀伤(NK)细胞近年来作为癌症免疫治疗的替代方案而受到关注。与基于 T 细胞的疗法相比,采用 NK 细胞的过继性细胞转移提供了一种更安全的治疗选择,因为其毒性显著更低,并且可获得多种自体及异体 NK 细胞来源。
然而,NK 细胞疗法仍面临若干挑战,包括体内持久性有限、免疫抑制性和敌对的肿瘤微环境(TME),以及缺乏针对实体瘤的有效治疗。为应对这些局限,已提出对 NK 细胞进行改造以稳定产生细胞因子,作为增强其持久性和增殖能力的策略。
此外,过表达激活性受体和阻断抑制性受体可恢复受 TME 抑制的 NK 细胞功能。为进一步改善肿瘤浸润和实体瘤的清除,已引入通过过表达趋化受体来增强 NK 细胞趋化性的创新方法。本综述重点介绍了研究激活性、抑制性和趋化性 NK 细胞受体工程化的临床前和临床研究的最新进展;讨论了细胞因子操控方面的近期进展;并探讨了将嵌合抗原受体(CAR)技术与 NK 细胞受体工程化相结合的潜力。
Natural killer (NK) cells have recently gained popularity as an alternative for cancer immunotherapy. Adoptive cell transfer employing NK cells offers a safer therapeutic option compared to T-cell-based therapies, due to their significantly lower toxicity and the availability of diverse autologous and allogeneic NK cell sources.
However, several challenges are associated with NK cell therapies, including limited in vivo persistence, the immunosuppressive and hostile tumor microenvironment (TME), and the lack of effective treatments for solid tumors. To address these limitations, the modification of NK cells to stably produce cytokines has been proposed as a strategy to enhance their persistence and proliferation.
Additionally, the overexpression of activating receptors and the blockade of inhibitory receptors can restore the NK cell functions hindered by the TME. To further improve tumor infiltration and the elimination of solid tumors, innovative approaches focusing on the enhancement of NK cell chemotaxis through the overexpression of chemotactic receptors have been introduced.
This review highlights the latest advancements in preclinical and clinical studies investigating the engineering of activating, inhibitory, and chemotactic NK cell receptors; discusses recent progress in cytokine manipulation; and explores the potential of combining the chimeric antigen receptor (CAR) technology with NK cell receptors engineering.
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