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:Development of allogeneic HSC-engineered iNKT cells for off-the-shelf cancer immunotherapy.
Development of allogeneic HSC-engineered iNKT cells for off-the-shelf cancer immunotherapy.
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基于细胞的免疫疗法已成为新一代的癌症药物,而能够大规模生产并随时分发给患者以治疗患者的“现货型”细胞产品是必要的。恒定自然杀伤T(iNKT)细胞是开发同种异体细胞疗法的理想细胞载体,因为它们是强大的免疫细胞,能够靶向癌症且无移植物抗宿主病(GvHD)风险。
然而,健康供者血液中内源性iNKT细胞数量极低。在此,通过结合造血干细胞(HSC)基因工程和体外分化,我们以高产率和纯度生成了人类同种异体HSC工程化iNKT(Allo HSC-iNKT)细胞;这些细胞与内源性iNKT细胞高度相似,通过多种机制有效靶向肿瘤细胞,并表现出高安全性和低免疫原性。这些细胞可进一步通过嵌合抗原受体(CAR)工程化改造以增强肿瘤靶向性,或/和通过基因编辑敲除表面人类白细胞抗原(HLA)分子以进一步降低免疫原性。
总体而言,这些临床前研究证明了Allo HSC-iNKT细胞产品的可行性和癌症治疗潜力,并为其转化和临床开发奠定了基础。
Cell-based immunotherapy has become the new-generation cancer medicine, and "off-the-shelf" cell products that can be manufactured at large scale and distributed readily to treat patients are necessary. Invariant natural killer T (iNKT) cells are ideal cell carriers for developing allogeneic cell therapy because they are powerful immune cells targeting cancers without graft-versus-host disease (GvHD) risk.
However, healthy donor blood contains extremely low numbers of endogenous iNKT cells.
Here, by combining hematopoietic stem cell (HSC) gene engineering and in vitro differentiation, we generate human allogeneic HSC-engineered iNKT ( Allo HSC-iNKT) cells at high yield and purity; these cells closely resemble endogenous iNKT cells, effectively target tumor cells using multiple mechanisms, and exhibit high safety and low immunogenicity.
These cells can be further engineered with chimeric antigen receptor (CAR) to enhance tumor targeting or/and gene edited to ablate surface human leukocyte antigen (HLA) molecules and further reduce immunogenicity. Collectively, these preclinical studies demonstrate the feasibility and cancer therapy potential of Allo HSC-iNKT cell products and lay a foundation for their translational and clinical development.
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