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:Automated manufacturing of clinical-grade BDCA2 CAR NK cells in a closed system for the treatment of blastic plasmacytoid dendritic cell neoplasm.
Automated manufacturing of clinical-grade BDCA2 CAR NK cells in a closed system for the treatment of blastic plasmacytoid dendritic cell neoplasm.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
嵌合抗原受体(CAR)自然杀伤(NK)细胞疗法的最新进展已证明其在癌症免疫治疗中具有广阔的应用前景。然而,目前大多数CAR NK细胞生产流程采用开放式系统并包含多个手工操作步骤,使得在临床应用中对治疗质量的一致性和法规合规性的维持面临挑战。
我们专门开发了靶向血液树突状细胞抗原2(BDCA2)的CAR NK细胞,用于治疗母细胞性浆细胞样树突状细胞肿瘤(BPDCN)。
在此,我们介绍一种在CliniMACS Prodigy平台上生产临床级CAR NK细胞的自动化、符合现行药品生产质量管理规范(cGMP)的NK 细胞转导(NKCT)工艺。该封闭系统整合了细胞分离、激活、转导、扩增和收获,从而降低了污染风险并确保细胞产品质量。NKCT工艺使用在cGMP条件下生产的狒狒包膜假型慢病毒载体(BaEV-LV)联合Vectofusin-1,实现了高转导效率,所获得的CAR NK细胞具有高活力和纯度。体外和体内研究均证明,CliniMACS Prodigy生产的BDCA2 CAR NK细胞具有强效抗肿瘤活性,凸显了其作为BPDCN治疗策略的潜力。
总之,该自动化NKCT工艺可实现集中式和分散式CAR NK生产,并促进CAR NK细胞疗法的高效临床转化。
Recent progress in chimeric antigen receptor (CAR) natural killer (NK) cell therapy has demonstrated their promising potential in cancer immunotherapy.
However, most current CAR NK cell manufacturing processes utilize open systems with multiple manual steps, making it challenging to maintain consistent therapeutic quality and regulatory compliance for clinical applications.
We specifically developed blood dendritic cell antigen 2 (BDCA2)-targeting CAR NK cells for treating blastic plasmacytoid dendritic cell neoplasm (BPDCN).
Here, we present an automated, current good manufacturing practice (cGMP)-compliant Natural Killer Cell Transduction (NKCT) process for producing clinical-grade CAR NK cells on the CliniMACS Prodigy platform. This closed system integrates cell separation, activation, transduction, expansion, and harvest, thereby reducing contamination risks and ensuring cell product quality.
The NKCT process achieved high transduction efficiency using baboon envelope pseudotyped lentiviral vectors (BaEV-LV) produced under cGMP conditions combined with Vectofusin -1, yielding CAR NK cells with high viability and purity.
Both in vitro and in vivo studies demonstrated the potent antitumor activity of CliniMACS Prodigy-manufactured BDCA2 CAR NK cells, highlighting a promising treatment strategy for BPDCN. In summary, this automated NKCT process enables both centralized and decentralized CAR NK manufacturing and facilitates the efficient clinical translation of CAR NK cell therapies.
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