Oncogenic cancer/testis antigens: prime candidates for immunotherapy

被引:252
作者
Gjerstorff, Morten F. [1 ]
Andersen, Mads H. [2 ]
Ditzel, Henrik J. [1 ,3 ]
机构
[1] Univ Southern Denmark, Dept Canc & Inflammat Res, Odense, Denmark
[2] Copenhagen Univ Hosp, Ctr Canc Immune Therapy CCIT, Dept Haematol, Herlev, Denmark
[3] Odense Univ Hosp, Dept Oncol, DK-5000 Odense, Denmark
关键词
cancer/testis antigen; oncogenesis; immunotherapy; CANCER-TESTIS ANTIGENS; MEIOSIS-SPECIFIC GENES; DOUBLE-STRAND BREAKS; MAGE-A; T-CELLS; MULTIPLE-MYELOMA; MESSENGER-RNA; MESENCHYMAL TRANSITION; CONFERS RESISTANCE; PROTEIN EXPRESSION;
D O I
10.18632/oncotarget.4694
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent developments have set the stage for immunotherapy as a supplement to conventional cancer treatment. Consequently, a significant effort is required to further improve efficacy and specificity, particularly the identification of optimal therapeutic targets for clinical testing. Cancer/testis antigens are immunogenic, highly cancer-specific, and frequently expressed in various types of cancer, which make them promising candidate targets for cancer immunotherapy, including cancer vaccination and adoptive T-cell transfer with chimeric T-cell receptors. Our current understanding of tumor immunology and immune escape suggests that targeting oncogenic antigens may be beneficial, meaning that identification of cancer/testis antigens with oncogenic properties is of high priority. Recent work from our lab and others provide evidence that many cancer/testis antigens, in fact, have oncogenic functions, including support of growth, survival and metastasis. This novel insight into the function of cancer/testis antigens has the potential to deliver more effective cancer vaccines. Moreover, immune targeting of oncogenic cancer/testis antigens in combination with conventional cytotoxic therapies or novel immunotherapies such as checkpoint blockade or adoptive transfer, represents a highly synergistic approach with the potential to improve patient survival.
引用
收藏
页码:15772 / 15787
页数:16
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