为肝细胞癌武装 GPC3 CAR-T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immune Checkpoint Inhibitors in HBV-Caused Hepatocellular Carcinoma Therapy.
Immune Checkpoint Inhibitors in HBV-Caused Hepatocellular Carcinoma Therapy.
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乙型肝炎病毒(HBV)感染是肝细胞癌(HCC)发生的主要风险因素,HCC 是最常见的肝癌类型,在全球范围内具有高发病率和死亡率。手术、肝移植和消融疗法已被用于治疗早期 HBV 引起的 HCC(HBV-HCC);同时,在晚期阶段,放化疗和药物靶向治疗通常被考虑,但疗效有限。近年来,免疫疗法,如肿瘤疫苗疗法、过继细胞转移疗法和免疫检查点抑制剂疗法,已在癌症治疗中显示出有前景的疗效。特别是,免疫检查点抑制剂能够成功阻止肿瘤实现免疫逃逸并促进抗肿瘤反应,从而提升 HBV-HCC 的治疗效果。
然而,免疫检查点抑制剂在 HBV-HCC 治疗中的优势仍有待开发。在此,我们描述 HBV-HCC 的基本特征和发生发展,并介绍当前 HBV-HCC 的治疗策略。
值得注意的是,我们综述了免疫检查点分子的原理,如程序性细胞死亡蛋白 1(PD-1)和细胞毒性 T 淋巴细胞相关蛋白 4(CTLA-4)在 HBV-HCC 中的作用,以及临床中正在考虑的相关抑制剂。
我们还讨论了免疫检查点抑制剂在 HBV-HCC 治疗中的益处,以及这些抑制剂在不同病因 HCC 中的疗效,旨在为免疫检查点抑制剂用于 HBV-HCC 治疗提供见解。
Hepatitis B virus (HBV) infection is the main risk factor for the development of hepatocellular carcinoma (HCC), the most common type of liver cancer, with high incidence and mortality worldwide. Surgery, liver transplantation, and ablation therapies have been used to treat early HBV-caused HCC (HBV-HCC); meanwhile, in the advanced stage, chemoradiotherapy and drug-targeted therapy are regularly considered, but with limited efficacy.
Recently, immunotherapies, such as tumor vaccine therapy, adoptive cell transfer therapy, and immune checkpoint inhibitor therapy, have demonstrated promising efficacy in cancer treatment. In particular, immune checkpoint inhibitors can successfully prevent tumors from achieving immune escape and promote an anti-tumor response, thereby boosting the therapeutic effect in HBV-HCC.
However, the advantages of immune checkpoint inhibitors in the treatment of HBV-HCC remain to be exploited.
Here, we describe the basic characteristics and development of HBV-HCC and introduce current treatment strategies for HBV-HCC. Of note, we review the principles of immune checkpoint molecules, such as programmed cell death protein 1(PD-1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) in HBV-HCC, as well as related inhibitors being considered in the clinic.
We also discuss the benefits of immune checkpoint inhibitors in the treatment of HBV-HCC and the efficacy of those inhibitors in HCC with various etiologies, aiming to provide insights into the use of immune checkpoint inhibitors for the treatment of HBV-HCC.
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