Department of Oncology, Haematology, Immuno-Oncology and Rheumatogy, University of Bonn, Bonn, Germany.
Clin Cancer Res. 2020 Sep 1;26(17):4442-4447. doi: 10.1158/1078-0432.CCR-20-0305. Epub 2020 May 1.
The introduction and the unexpected efficacy of checkpoint inhibitors (CPI) and more recently of chimeric antigen receptor T cells (CAR T-cells) in the treatment of malignant diseases boosted the efforts in the development and clinical application of immunotherapeutic approaches. However, the definition of predictive factors associated with clinical responses as well as the identification of underlying mechanisms that promote the therapeutic efficacy remain to be determined. Starting from the first immunotherapeutic trials, it became evident that vaccine-induced tumor-specific T cells or the adoptive transfer of -expanded T lymphocytes can recognize and eliminate malignant cells leading to long-lasting remissions in some patients. In addition, a phenomenon called epitope spreading, which was observed in responding patients, seemed to increase the efficiency possibly representing an important predictive factor. This review will focus on experimental and clinical evidence for the induction of epitope spreading and its role in the maintenance of an efficient antitumor immune response in cancer immunotherapy.
在恶性疾病的治疗中,检查点抑制剂(CPI)的引入和出人意料的疗效,以及最近嵌合抗原受体 T 细胞(CAR T 细胞)的应用,推动了免疫治疗方法的开发和临床应用。然而,与临床反应相关的预测因素的定义以及促进治疗疗效的潜在机制的确定仍有待确定。从第一个免疫治疗试验开始,就很明显,疫苗诱导的肿瘤特异性 T 细胞或扩增的 T 淋巴细胞的过继转移可以识别和消除恶性细胞,从而导致一些患者的长期缓解。此外,在应答患者中观察到的一种称为表位扩展的现象似乎提高了效率,可能是一个重要的预测因素。这篇综述将重点介绍在癌症免疫治疗中诱导表位扩展的实验和临床证据及其在维持有效的抗肿瘤免疫反应中的作用。