3D 打印植入式 CAR-巨噬细胞用于术后癌症免疫治疗
3D-printed implantable CAR-macrophages for post-surgery cancer immunotherapy.
FRONTIER PAPERS
3D-printed implantable CAR-macrophages for post-surgery cancer immunotherapy.
Synthetic SIGLEC9-based chimeric switch receptor augments the efficacy of CAR macrophages against glioblastoma.
Armored bicistronic CAR T cells with dominant-negative TGF-β receptor II to overcome resistance in glioblastoma.
Chimeric antigen receptor T cell therapy for glioblastoma: overcoming current barriers and strategies to enhance efficacy for therapeutic implications
CAR T cells: engineered immune cells to treat brain cancers and beyond.
Locally secreted BiTEs complement CAR T cells by enhancing killing of antigen heterogeneous solid tumors.
DPP4 promotes an immunoenhancing tumor microenvironment through exhausted CD8+ T cells with activating IL13-IL13RA2 axis in papillary thyroid cancer.
阻断 DPP4 导致耗竭的 CD8+ T 细胞转化,IL13 水平降低,进而下调 IL13RA2,促进 PTC 细胞的间质-上皮转化。这突显了 DPP4 作为潜在治疗靶点,特别是在 CD8+ T 细胞与 PTC 细胞之间通过 IL13-IL13RA2 轴,并为 PTC 的联合免疫治疗代表了一条新途径。
IL13Rα2-targeted third-generation CAR-T cells with CD28 transmembrane domain mediate the best anti-glioblastoma efficacy.
Advancing glioblastoma immunotherapy: Molecular pathways and innovative therapeutic strategies.
Unveiling the expression and mechanistic role of SYCP2 in cervical lesions.
SYCP2 成为 HPV 驱动宫颈癌变的关键生物标志物,对高级别病变具有诊断潜力,对转移风险具有预后价值。其在 IL13RA2 介导的信号传导中的调控作用以及与病毒应答通路的关联,提示其机制性参与肿瘤微环境重塑。这种双重的情境依赖性表达(在宫颈癌中上调而在其他恶性肿瘤中下调)凸显了组织特异性的致癌功能。这些发现使 SYCP2 成为 HPV 相关宫颈癌筛查和治疗策略的有前景的靶点。
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