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:GMP-Based Isolation of Full-Term Human Placenta-Derived NK Cells for CAR-NK Cell Therapy in Malignant Melanoma.
GMP-Based Isolation of Full-Term Human Placenta-Derived NK Cells for CAR-NK Cell Therapy in Malignant Melanoma.
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黑色素瘤是一种严重的皮肤癌,因对现有治疗耐受而难以管理。尽管如此,黑色素瘤免疫原性较高,适合采用免疫疗法;自然杀伤(NK)细胞也已被证实具有抗肿瘤作用。嵌合抗原受体(CAR)修饰NK细胞,即CAR-NK细胞,有望增强免疫治疗方案。为此,研究者探索了多种NK细胞来源,包括胎盘来源细胞。与其他来源相比,胎盘来源NK细胞具有一定优势,但其体外扩增能力有限。近期研究显示,可从胎盘来源细胞体外扩增出具有功能且具有抗肿瘤细胞毒性的NK细胞。本章介绍依据药品生产质量管理规范(GMP)方法分离足月人胎盘来源NK细胞,用于黑色素瘤CAR-NK细胞治疗。
Melanoma, a severe type of skin cancer, poses significant management challenges due to its resistance to available treatments. Despite this obstacle, the high immunogenicity of melanoma renders it amenable to immune therapy, and NK cells have been identified as possessing anti-tumor properties in immunotherapy. The development of chimeric antigen receptor (CAR)-modified NK cells, or CAR-NK cells, has shown potential in enhancing immunotherapeutic regimens.
To achieve this, researchers have explored various sources of NK cells, including those derived from the placenta, which offers benefits compared to other sources due to their limited ex vivo expansion potential. Recent studies have indicated the capacity to expand functional NK cells from placenta-derived cells in vitro that possess anti-tumor cytolytic properties. This chapter discusses the isolation of full-term human placenta-derived NK cells using Good Manufacturing Practice-based methods for CAR-NK cell therapy in melanoma.
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