基于器官囊过滤的胰腺靶向脂质纳米颗粒
Pancreatic-targeted lipid nanoparticles based on organ capsule filtration.
实现胰腺靶向递送是治疗胰腺疾病的一项突破,但精准递送仍具挑战性 1。
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Pancreatic-targeted lipid nanoparticles based on organ capsule filtration.
实现胰腺靶向递送是治疗胰腺疾病的一项突破,但精准递送仍具挑战性 1。
SLC25A51 mRNA-LNP Armors T Cells with Mitochondrial Fitness in Cancer Treatment.
由于代谢恶劣的肿瘤微环境损害线粒体功能,胰腺导管腺癌对过继性 T 细胞疗法仍大多难治。
CpG 1018 augments mRNA vaccine-induced anti-tumor immunity by potentiating CD8+ T cell responses.
CpG 1018佐剂mRNA疫苗引起一过性体重下降(<6%),总体安全性良好。
In vivo FAP-CAR macrophages enhance chemotherapy and immunotherapy against pancreatic cancer by removing the fibrosis barrier.
我们的结果表明,mRNA-MLNP能有效将M2巨噬细胞重编程为FAP-CAR-M。
Clinical translation of mRNA-based cancer vaccines for solid tumors.
使用信使RNA(mRNA)的疫苗已成为一个有前景的平台,正在改变癌症免疫治疗。
Advances in the Management of Pancreatic Cancer: Current Strategies and Emerging Therapies.
胰腺导管腺癌(PDAC)仍然是一种极为凶险的恶性肿瘤,其发病率不断上升,长期生存率极低,这主要归因于晚期就诊和固有的治疗耐药性。
TGFB2 Gene Methylation in Tumors with Low CD8(+) T-Cell Infiltration Drives Positive Prognostic Overall Survival Responses in Pancreatic Ductal Adenoc
使用中位截断值绘制KM曲线分析TGFB2、TGFB3和IFI27基因甲基化,结果显示TGFB2、IFI27和TGFB3基因高甲基化水平分别使中位总生存期显著延长5.7个月(p = 0.044)、5.2个月(p = 0.036)和3.7个月(p = 0.028)。
Flagellin co-expression potentiates mRNA vaccine-induced cytotoxic T lymphocyte responses but not anti-tumor immunity.
这些结果支持通过鞭毛蛋白共表达来增强mRNA疫苗诱导的CTL反应,但仍需制定策略以促进所诱导的外周CTL向肿瘤浸润。
Novel mRNA-Engineered Fully Human CAR-T Cells Targeting AXL in Solid Tumors.
结果:流式细胞术证实 CAR 呈短暂但高表达(24 h 时 >90%),且 T 细胞活力保持(>90%)。
mRNA vaccines in cancer immunotherapy: current progress and perspectives in solid tumors and hematologic malignancies.
COVID-19大流行期间mRNA疫苗的空前成功加速了基于核酸的治疗方法的发展,尤其是在肿瘤学领域。
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