西罗莫司通过肿瘤选择性增强病毒复制提高溶瘤病毒 M1 的疗效
Sirolimus potentiates oncolytic Virus M1 efficacy through tumor-selective augmentation of viral replication.
西罗莫司通过 mTOR 抑制和 I 型干扰素信号抑制,选择性增强肿瘤内的病毒复制,从而增强 M1 溶瘤病毒疗法,且不依赖于 CD8 T 细胞介导的免疫。
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Sirolimus potentiates oncolytic Virus M1 efficacy through tumor-selective augmentation of viral replication.
西罗莫司通过 mTOR 抑制和 I 型干扰素信号抑制,选择性增强肿瘤内的病毒复制,从而增强 M1 溶瘤病毒疗法,且不依赖于 CD8 T 细胞介导的免疫。
Extracellular vesicles as signal hubs and targeted platforms in hepatocellular carcinoma immunotherapy.
免疫治疗已改变肝细胞癌(HCC)的管理,但其疗效常受免疫抑制性肿瘤微环境(TME)的限制。
From Bench to Bedside: Emerging Paradigms in CAR-T Cell Therapy for Solid Malignancies.
免疫治疗,尤其是CAR-T 细胞疗法,已经彻底改变了血液系统恶性肿瘤和自身免疫性疾病的治疗。
Immunosuppressive tumor microenvironment and immunotherapy of hepatocellular carcinoma: current status and prospectives.
肝细胞癌(HCC)是全球主要的健康问题,治疗方案有限,预后较差。
Systemic delivery of glycosylated-PEG-masked oncolytic virus enhances targeting of antitumor immuno-virotherapy and modulates T and NK cell infiltrati
依据:免疫病毒治疗已成为一种有前景的癌症治疗手段,因为它可通过全身免疫刺激直接以细胞毒方式清除肿瘤。
Converting 'cold' to 'hot' hepatocellular carcinoma for improved immunotherapy (Review).
肝细胞癌(HCC)常表现出免疫“冷”肿瘤微环境(TME),其特征为T细胞浸润不良和免疫抑制机制活跃,限制了免疫检查点抑制剂(ICIs)等免疫疗法的疗效。
Engineered oncolytic herpes simplex virus expressing interleukin 12 suppresses tumorigenicity of hepatocellular carcinoma.
溶瘤病毒(OVs)通过直接溶瘤活性和免疫调节转基因的表达介导抗癌效应。
A conceptual exploration on the synergistic anti-tumor effects of high-order combination of OHSV2-DSTE(FAP5/CD3), CAR-T cells, and immunotoxins in hep
这种高阶联合代表了一种针对肝细胞癌的新型多波次免疫治疗策略。
Oncolytic virus encoding 4-1BBL and IL15 enhances the efficacy of tumor-infiltrating lymphocyte adoptive therapy in HCC.
既往研究发现,溶瘤病毒(OVs)可提高 TIL 过继疗法在口腔癌、结肠癌和胰腺癌中的疗效。
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