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:The Application of iPSCs in Tumour Immunotherapy.
The Application of iPSCs in Tumour Immunotherapy.
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本文全面综述了 iPSCs 在肿瘤免疫治疗中的应用,并探讨了这一不断发展领域中的机遇与挑战。
肿瘤免疫治疗作为癌症治疗的一种方法具有巨大前景,癌症是全球第二大死亡原因。这种治疗方法大致可分为两种主要类型:主动免疫治疗和被动或过继性免疫治疗。主动免疫治疗,如癌症疫苗,刺激患者的免疫系统靶向肿瘤细胞。另一方面,过继性免疫治疗涉及向患者提供体外激活的免疫细胞,如T细胞、NK 细胞和巨噬细胞,以对抗肿瘤。诱导多能干细胞由于其多能性和易于基因编辑,在主动和过继性肿瘤免疫治疗中均被广泛利用。它们可以分化为各种类型的免疫细胞用于直接癌症治疗,也可以作为肿瘤疫苗引发针对肿瘤的免疫反应。重要的是,iPSCs可以被利用来开发即用型同种异体免疫治疗产品。
Tumour immunotherapy holds great promise as a treatment for cancer, which ranks as the second highest cause of mortality worldwide. This therapeutic approach can be broadly categorized into two main types: active immunotherapy and passive or adoptive immunotherapy. Active immunotherapy, such as cancer vaccines, stimulates the patients' immune system to target tumour cells. On the other hand, adoptive immunotherapy involves supplying in vitro activated immune cells, such as T cells, natural killer cells and macrophages, to the patient to combat the tumour. Induced pluripotent stem cells are extensively utilized in both active and adoptive tumour immunotherapy due to their pluripotency and ease of gene editing. They can be differentiated into various types of immune cells for direct cancer treatment and can also function as tumour vaccines to elicit an immune response against the tumour. Importantly, iPSCs can be leveraged to develop off-the-shelf allogenic immunotherapy products.
This article provides a comprehensive review of the application of iPSCs in tumor immunotherapy, along with a discussion of the opportunities and challenges in this evolving field.
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