丙戊酸钠驱动丙酰化介导的表观遗传重编程以增强间皮素 CAR-T 细胞治疗实体瘤
Sodium valproate drives propionylation-mediated epigenetic reprogramming to enhance mesothelin CAR-T cell therapy in solid tumors.
FRONTIER PAPERS
Sodium valproate drives propionylation-mediated epigenetic reprogramming to enhance mesothelin CAR-T cell therapy in solid tumors.
Targeting triple-negative breast cancer using cord-blood CD34⁺ HSPC-derived mesothelin-specific CAR-NKT cells with potent antitumor activity.
这些结果支持 Allo15 MCAR-NKT 细胞作为一种下一代、现成的免疫疗法,对 TNBC 具有强大的治疗潜力,特别是在转移、免疫逃逸和治疗耐药的情况下。
Chimeric antigen receptor NK cells for breast cancer immunotherapy.
Mesothelin-targeted CAR-T cells secreting NKG2D-BiTEs exhibit potent efficacy against triple-negative breast cancer.
Proton pump inhibitor attenuates acidic microenvironment to improve the therapeutic effects of MSLN-CAR-T cells on the brain metastasis.
Microenvironmental alkalization promotes the therapeutic effects of MSLN-CAR-T cells.
Chimeric antigen receptor T cells as adjuvant therapy for unresectable adenocarcinoma.
Chimeric antigen receptor T cells engineered to recognize the P329G-mutated Fc part of effector-silenced tumor antigen-targeting human IgG1 antibodies
靶向 P329G 的 CAR-T 细胞联合含 P329G Fc 突变的人 IgG1 抗原结合抗体,在不同实体瘤模型中介导了显著的体外和体内效应功能,值得进一步推进该概念的临床转化。
A Phase I Trial of Regional Mesothelin-Targeted CAR T-cell Therapy in Patients with Malignant Pleural Disease, in Combination with the Anti-PD-1 Agent
Knowledge mapping and research trends of chimeric antigen receptor T-cell immunotherapy in breast cancer: A bibliometric and visual analytics study.
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