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:Human pluripotent stem cell-derived innate and adaptive immune cells for cancer immunotherapy.
Human pluripotent stem cell-derived innate and adaptive immune cells for cancer immunotherapy.
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异体细胞疗法在癌症免疫治疗中前景广阔,但面临规模化、免疫排斥、移植物抗宿主病和毒性等挑战。人多能干细胞(hPSC),包括胚胎干细胞和诱导多能干细胞(iPSC),提供了可规模化、适应性强的平台,有望克服这些局限。hPSC可作为取之不尽的免疫细胞来源,并能在单细胞水平进行基因改造,以增强抗肿瘤活性、降低免疫原性。近期iPSC来源自然杀伤(NK)细胞、T细胞和巨噬细胞制备进展,为更安全、更有效的免疫疗法打开了道路。本综述考察利用hPSC来源免疫细胞增强癌症治疗的进展、挑战和未来方向,并探讨其克服异体治疗障碍的潜力。
Allogeneic cell-based therapies hold great promise for cancer immunotherapy but face challenges like scalability, immune rejection, graft-versus-host disease, and toxicities. Human pluripotent stem cells (hPSCs), including embryonic and induced pluripotent stem cells (iPSCs), offer a scalable and adaptable platform to address these limitations.
hPSCs provide an inexhaustible source of immune cells that can be genetically modified at the single-cell level to enhance anti-tumor activity and reduce immunogenicity. Recent advancements in generating iPSC-derived natural killer (NK) cells, T cells, and macrophages are opening the door to safer and more effective immunotherapies. This review examines the progress, challenges, and future directions in utilizing hPSC-derived immune cells to enhance cancer treatment and overcome barriers in allogeneic therapy.
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