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:Research progress in leveraging biomaterials for enhancing NK cell immunotherapy.
Research progress in leveraging biomaterials for enhancing NK cell immunotherapy.
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NK细胞免疫治疗是继T细胞免疫治疗发展之后一种有前景的抗肿瘤治疗方式。利用生物材料对NK细胞进行结构修饰,可能提供一种精准、高效且低成本的策略来增强NK细胞免疫治疗。NK细胞的生物材料修饰可分为两种策略:利用生物材料的表面工程和细胞内修饰。表面工程策略包括脂质的疏水相互作用、膜蛋白之间的受体-配体相互作用、与氨基酸残基的共价结合、点击反应和静电相互作用。细胞内修饰策略基于利用来自各种来源NK细胞的膜性材料(如外泌体、囊泡和细胞膜)通过纳米技术进行操控。
最后,基于生物材料的策略在原位调控实体瘤部位NK细胞的募集、识别和细胞毒性,以增强肿瘤中NK细胞的活性。本文综述了基于生物材料修饰增强NK细胞治疗的最新研究进展,为进一步研究利用生物材料工程化NK细胞治疗提供参考。NK T NK NK - NK NK NK NK NK NK NK NK NK NK . NK细胞免疫治疗是继T细胞免疫治疗发展之后一种有前景的抗肿瘤治疗方式。利用生物材料对NK细胞进行结构修饰,可能提供一种精准、高效且低成本的策略来增强NK细胞免疫治疗。NK细胞的生物材料修饰可分为两种策略:利用生物材料的表面工程和细胞内修饰。表面工程策略包括脂质的疏水相互作用、膜蛋白之间的受体-配体相互作用、与氨基酸残基的共价结合、点击反应和静电相互作用。细胞内修饰策略基于利用来自各种来源NK细胞的膜性材料(如外泌体、囊泡和细胞膜)的纳米技术操作。
最后,基于生物材料的策略在原位调控实体瘤部位NK细胞的募集、识别和细胞毒性,以增强肿瘤中NK细胞的活性。本文综述了基于生物材料修饰增强NK细胞治疗的最新研究进展,为进一步研究利用生物材料工程化NK细胞治疗提供参考。
NK cell immunotherapy is a promising antitumor therapeutic modality after the development of T cell immunotherapy. Structural modification of NK cells with biomaterials may provide a precise, efficient, and low-cost strategy to enhance NK cell immunotherapy. The biomaterial modification of NK cells can be divided into two strategies: surface engineering with biomaterials and intracellular modification.
The surface engineering strategies include hydrophobic interaction of lipids, receptor-ligand interaction between membrane proteins, covalent binding to amino acid residues, click reaction and electrostatic interaction. The intracellular modification strategies are based on manipulation by nanotechnology using membranous materials from various sources of NK cells (such as exosome, vesicle and cytomembranes).
Finally, the biomaterials-based strategies regulate the recruitment, recognition and cytotoxicity of NK cells in the solid tumor site in situ to boost the activity of NK cells in the tumor. This article reviews the recent research progress in enhancing NK cell therapy based on biomaterial modification, to provide a reference for further researches on engineering NK cell therapy with biomaterials. NK T NK NK - NK NK NK NK NK NK NK NK NK NK . NK cell immunotherapy is a promising antitumor therapeutic modality after the development of T cell immunotherapy.
Structural modification of NK cells with biomaterials may provide a precise, efficient, and low-cost strategy to enhance NK cell immunotherapy. The biomaterial modification of NK cells can be divided into two strategies: surface engineering with biomaterials and intracellular modification.
The surface engineering strategies include hydrophobic interaction of lipids, receptor-ligand interaction between membrane proteins, covalent binding to amino acid residues, click reaction and electrostatic interaction. The intracellular modification strategies are based on manipulation by nanotechnology using membranous materials from various sources of NK cells (such as exosome, vesicle and cytomembranes).
Finally, the biomaterials-based strategies regulate the recruitment, recognition and cytotoxicity of NK cells in the solid tumor site in situ to boost the activity of NK cells in the tumor. This article reviews the recent research progress in enhancing NK cell therapy based on biomaterial modification, to provide a reference for further researches on engineering NK cell therapy with biomaterials.
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