Urbanova Linda, Hradilova Nada, Moserova Irena, Vosahlikova Sarka, Sadilkova Lenka, Hensler Michal, Spisek Radek, Adkins Irena
SOTIO, Prague, Czech Republic; Department of Immunology, 2nd Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
SOTIO, Prague, Czech Republic.
Immunol Lett. 2017 Jul;187:27-34. doi: 10.1016/j.imlet.2017.05.005. Epub 2017 May 8.
High hydrostatic pressure (HHP) can be used to generate dendritic cell (DC)-based active immunotherapy for prostate, lung and ovarian cancer. We showed here that HHP treatment of selected human cancer cell lines leads to a degradation of tumor antigens which depends on the magnitude of HHP applied and on the cancer cell line origin. Whereas prostate or ovarian cell lines displayed little protein antigen degradation with HHP treatment up to 300MPa after 2h, tumor antigens are hardly detected in lung cancer cell line after treatment with HHP 250MPa at the same time. On the other hand, quick reduction of tumor antigen-coding mRNA was observed at HHP 200MPa immediately after treatment in all cell lines tested. To optimize the DC-based active cellular therapy protocol for HHP-sensitive cell lines the immunogenicity of HHP-treated lung cancer cells at 150, 200 and 250MPa was compared. Lung cancer cells treated with HHP 150MPa display characteristics of immunogenic cell death, however cells are not efficiently phagocytosed by DC. Despite induction of the highest number of antigen-specific CD8 T cells, 150 MPa-treated lung cancer cells survive in high numbers. This excludes their use in DC vaccine manufacturing. HHP of 200MPa treatment of lung cancer cells ensures the optimal ratio of efficient immunogenic killing and delivery of protein antigens in DC. These results represent an important pre-clinical data for generation of immunogenic killed lung cancer cells in ongoing NSCLC Phase I/II clinical trial using DC-based active cellular immunotherapy (DCVAC/LuCa).
高静水压(HHP)可用于生成基于树突状细胞(DC)的前列腺癌、肺癌和卵巢癌主动免疫疗法。我们在此表明,对选定的人类癌细胞系进行HHP处理会导致肿瘤抗原降解,这取决于所施加的HHP大小以及癌细胞系的来源。在2小时内,高达300MPa的HHP处理对前列腺或卵巢癌细胞系的蛋白质抗原降解作用较小,而在相同时间用250MPa的HHP处理后,肺癌细胞系中几乎检测不到肿瘤抗原。另一方面,在所有测试的细胞系中,处理后立即在200MPa的HHP条件下观察到肿瘤抗原编码mRNA的快速减少。为了优化针对HHP敏感细胞系的基于DC的主动细胞治疗方案,比较了在150、200和250MPa下HHP处理的肺癌细胞的免疫原性。用150MPa的HHP处理的肺癌细胞表现出免疫原性细胞死亡的特征,然而细胞不能被DC有效吞噬。尽管诱导了数量最多的抗原特异性CD8 T细胞,但150MPa处理的肺癌细胞仍大量存活。这排除了它们在DC疫苗生产中的应用。200MPa的HHP处理肺癌细胞可确保在DC中高效免疫原性杀伤和蛋白质抗原递送的最佳比例。这些结果代表了在正在进行的使用基于DC的主动细胞免疫疗法(DCVAC/LuCa)的非小细胞肺癌I/II期临床试验中生成免疫原性杀伤肺癌细胞的重要临床前数据。