Alsalloum Alaa, Shevchenko Julia A, Sennikov Sergey
Laboratory of Molecular Immunology, Federal State Budgetary Scientific Institution Research Institute of Fundamental and Clinical Immunology, 630099 Novosibirsk, Russia.
Faculty of Natural Sciences, Novosibirsk State University, 630090 Novosibirsk, Russia.
Cancers (Basel). 2023 Mar 15;15(6):1779. doi: 10.3390/cancers15061779.
Early efforts to identify tumor-associated antigens over the last decade have provided unique cancer epitopes for targeted cancer therapy. MAGE-A proteins are a subclass of cancer/testis (CT) antigens that are presented on the cell surface by MHC class I molecules as an immune-privileged site. This is due to their restricted expression to germline cells and a wide range of cancers, where they are associated with resistance to chemotherapy, metastasis, and cancer cells with an increasing potential for survival. This makes them an appealing candidate target for designing an effective and specific immunotherapy, thereby suggesting that targeting oncogenic MAGE-As with cancer vaccination, adoptive T-cell transfer, or a combination of therapies would be promising. In this review, we summarize and discuss previous and ongoing (pre-)clinical studies that target these antigens, while bearing in mind the benefits and drawbacks of various therapeutic strategies, in order to speculate on future directions for MAGE-A-specific immunotherapies.
在过去十年中,早期识别肿瘤相关抗原的努力为靶向癌症治疗提供了独特的癌症表位。MAGE-A蛋白是癌/睾丸(CT)抗原的一个亚类,由MHC I类分子呈递在细胞表面,作为一个免疫特惠位点。这是因为它们在生殖细胞和多种癌症中表达受限,在这些癌症中,它们与化疗耐药、转移以及生存潜力不断增加的癌细胞相关。这使得它们成为设计有效且特异性免疫疗法的有吸引力的候选靶点,从而表明通过癌症疫苗接种、过继性T细胞转移或联合疗法靶向致癌性MAGE-A将大有可为。在这篇综述中,我们总结并讨论了之前和正在进行的针对这些抗原的(临床前)临床研究,同时牢记各种治疗策略的优缺点,以便推测MAGE-A特异性免疫疗法的未来方向。