Department of Medicine II, University of Freiburg, Germany.
Dig Dis. 2012;30(5):483-91. doi: 10.1159/000341697. Epub 2012 Oct 24.
Hepatocellular carcinoma (HCC) is the fifth most common cancer worldwide, with a continuously high mortality. Thus, the development of new therapeutic strategies is crucial to decrease recurrence rates and to improve the overall survival rates of HCC patients. The rationale for immunotherapy is based on the findings of several studies showing specific CD8(+) T-cell responses against various tumor-associated antigens (TAAs) in HCC patients and a clinical benefit of T-cell infiltration in the tumor tissue. However, the impact of TAA-specific CD8(+) T-cell responses on tumor control seems to be rather weak. Several different mechanisms contribute to the failure of the cellular immune response and will be summarized in this review. The aim of immune-based therapies is to overcome these mechanisms of T-cell failure and to induce or boost TAA-specific CD8(+) and CD4(+) T-cell responses. Several preclinical and clinical studies of immune-based therapeutic approaches show encouraging results and will be discussed in this review.
肝细胞癌(HCC)是全球第五大常见癌症,死亡率一直居高不下。因此,开发新的治疗策略对于降低复发率和提高 HCC 患者的总生存率至关重要。免疫疗法的基本原理基于以下发现:多项研究显示 HCC 患者存在针对各种肿瘤相关抗原(TAA)的特异性 CD8(+) T 细胞反应,以及肿瘤组织中 T 细胞浸润具有临床获益。然而,TAA 特异性 CD8(+) T 细胞反应对肿瘤控制的影响似乎相当微弱。有几个不同的机制导致细胞免疫反应失败,这将在本综述中进行总结。免疫治疗的目的是克服 T 细胞衰竭的这些机制,并诱导或增强 TAA 特异性 CD8(+) 和 CD4(+) T 细胞反应。本综述将讨论几种免疫治疗方法的临床前和临床研究结果,这些研究结果令人鼓舞。