de Duve Institute, UCLouvain, Brussels, Belgium.
Immunology Programme, The Babraham Institute, Cambridge, United Kingdom.
Clin Cancer Res. 2023 Jan 17;29(2):309-315. doi: 10.1158/1078-0432.CCR-21-3798.
T cells are key effectors of our immune response against tumors and exert their antitumor effects upon recognizing a variety of tumor-specific peptides presented by HLA molecules on the surface of tumor cells. The identification of the tumor-specific antigens of a given tumor is not required for immune checkpoint therapy (ICT), which mainly reactivates existing tumor-specific T cells together with T cells of unknown specificities. To decrease the activation of non-tumor-specific T cells, active or passive immunizations against tumor-specific antigens are considered. These immunizations require the identification of at least some of the tumor-specific antigens displayed on the tumor cells of a patient. While this has become an easy task for tumors with a large number of mutations generating neoantigens, it remains difficult for the remainder. Here, we review some facts about human tumor-specific or tumor-associated antigens, as well as some hopes for their future use in cancer immunotherapy.
T 细胞是我们针对肿瘤的免疫反应的关键效应器,它们通过识别肿瘤细胞表面 HLA 分子呈递的各种肿瘤特异性肽来发挥抗肿瘤作用。免疫检查点治疗 (ICT) 不需要确定特定肿瘤的肿瘤特异性抗原,它主要重新激活现有的肿瘤特异性 T 细胞和未知特异性的 T 细胞。为了减少非肿瘤特异性 T 细胞的激活,可以考虑针对肿瘤特异性抗原进行主动或被动免疫。这些免疫接种需要识别至少一些患者肿瘤细胞上显示的肿瘤特异性抗原。虽然对于产生新抗原的突变数量较多的肿瘤来说,这已经成为一项简单的任务,但对于其余肿瘤来说仍然很困难。在这里,我们回顾了一些关于人类肿瘤特异性或肿瘤相关抗原的事实,以及它们在癌症免疫治疗中的未来应用的一些希望。