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:NK cells encapsulated in micro/macropore-forming hydrogels via 3D bioprinting for tumor immunotherapy.
NK cells encapsulated in micro/macropore-forming hydrogels via 3D bioprinting for tumor immunotherapy.
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我们证明,封装 NK 细胞的水凝胶通过 3D 生物打印为 NK 细胞疗法在白血病和实体瘤中的临床应用创造了合适的微宏观环境。3D 生物打印使宏观尺度的临床应用成为可能,其自动化流程显示出作为现货型免疫治疗产品开发的潜力。该免疫治疗系统可为预防肿瘤切除后的肿瘤复发和转移提供一种临床选择。通过 3D 生物打印制备并植入肿瘤部位的载 NK 细胞的微/大孔成形水凝胶。
实体瘤在手术切除后若残留部分病灶或无法完全切除,患者将面临严重威胁。免疫治疗作为预防这一状况的方法已引起关注。然而,针对实体瘤的常规免疫治疗方法,即静脉注射,在归巢至肿瘤和体内扩增方面存在局限性,且尚未显示出有效的临床结果。
为克服这些局限性,利用3D生物打印技术将NK 细胞封装于可形成微孔/大孔的水凝胶中,以靶向实体瘤。采用海藻酸钠和明胶制备微-大孔水凝胶。由于明胶的热敏感性,海藻酸钠水凝胶中所含的明胶被去除,从而在明胶释放的位置生成相互连通的微孔。因此,可以通过生物打印形成大孔,并利用热敏性明胶形成微孔,从而制得大孔水凝胶。
已证实,有意形成的微孔可帮助NK细胞更容易聚集,从而增强细胞活力、裂解活性和细胞因子释放。大孔可利用3D生物打印形成,这使NK细胞能够获得必需元素。我们还表征了NK 92和zEGFR-CAR-NK细胞在成孔水凝胶中的功能。利用体外模型研究了其对白血病和实体瘤的抗肿瘤作用。
Patients face a serious threat if a solid tumor leaves behind partial residuals or cannot be completely removed after surgical resection. Immunotherapy has attracted attention as a method to prevent this condition. However, the conventional immunotherapy method targeting solid tumors, that is, intravenous injection, has limitations in homing in on the tumor and in vivo expansion and has not shown effective clinical results. METHOD: To overcome these limitations, NK cells (Natural killer cells) were encapsulated in micro/macropore-forming hydrogels using 3D bioprinting to target solid tumors. Sodium alginate and gelatin were used to prepare micro-macroporous hydrogels. The gelatin contained in the alginate hydrogel was removed because of the thermal sensitivity of the gelatin, which can generate interconnected micropores where the gelatin was released. Therefore, macropores can be formed through bioprinting and micropores can be formed using thermally sensitive gelatin to make macroporous hydrogels.
It was confirmed that intentionally formed micropores could help NK cells to aggregate easily, which enhances cell viability, lysis activity, and cytokine release. Macropores can be formed using 3D bioprinting, which enables NK cells to receive the essential elements. We also characterized the functionality of NK 92 and zEGFR-CAR-NK cells in the pore-forming hydrogel. The antitumor effects on leukemia and solid tumors were investigated using an in vitro model.
We demonstrated that the hydrogel encapsulating NK cells created an appropriate micro-macro environment for clinical applications of NK cell therapy for both leukemia and solid tumors via 3D bioprinting. 3D bioprinting makes macro-scale clinical applications possible, and the automatic process shows potential for development as an off-the-shelf immunotherapy product. This immunotherapy system could provide a clinical option for preventing tumor relapse and metastasis after tumor resection. Micro/macropore-forming hydrogel with NK cells fabricated by 3D bioprinting and implanted into the tumor site.
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