靶向 EGFR 的 IgG1 抗体增强 KRAS 突变胰腺癌中 NK 细胞介导的肿瘤杀伤
EGFR-Targeting IgG1 Antibody Enhances NK Cell-Mediated Tumor Killing in KRAS-Mutant Pancreatic Cancer.
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EGFR-Targeting IgG1 Antibody Enhances NK Cell-Mediated Tumor Killing in KRAS-Mutant Pancreatic Cancer.
The TGF-βR1 inhibitor galunisertib re-shapes the PDAC-TME by limiting decidual-like natural killer cells polarization.
In situ blockade of TNF-TNFR2 axis via oncolytic adenovirus improves antitumor efficacy in solid tumors.
Engineering NKG2D ligand affinity transforms EGFR-targeted NK cell engagers into high-potency effectors against pancreatic cancer.
这些结果支持了在此评估的 EGFR 靶向、Fc 功能性格式中 NKG2D 参与型 ICEs 的亲和力-活性关系。值得注意的是,提高 ULBP6 亲和力增强了 NK 细胞效应功能,并在 NK 重建的 PDAC 模型中提高了抗肿瘤疗效。总体而言,我们的发现为工程化高 potency、肿瘤锚定的 NKG2D 参与剂用于免疫冷肿瘤如 PDAC 的免疫治疗提供了设计框架。
Tumor-associated Tn and STn antigens: from molecular mechanism to precision diagnosis and treatment.
Tn/STn 抗原在肿瘤发生和免疫逃逸中发挥关键作用,在诊断和治疗方面具有巨大潜力。未来研究应集中于阐明其潜在机制、开发创新检测技术,并促进多学科合作,以推动基于 Tn/STn 抗原的肿瘤分子分型、精准靶向治疗和疗效预测系统的发展,从而为癌症诊断和治疗提供新方向。
Recurrent pancreatic cancer treated with N-803 and PD-L1 t-haNK followed by an EGFR-targeted nanocell drug conjugate.
Cetuximab-mediated antibody-dependent cell-mediated cytotoxicity enhances anti-tumor efficacy of patient-derived natural killer cells in pancreatic ca
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