Research advance in tumor specific antigens: a narrative review

Yusuke Takahashi, Ayako Demachi‐Okamura, Y. Oya, Takeo Nakada, N. Sakakura, H. Kuroda, H. Matsushita
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引用次数: 2

Abstract

Whether or not there are “tumor antigens” recognized by T cells had been controversial, until mouse and human tumor antigens have been identified one after another since the 1980s. In recent years, advances in genome sequencing technology has made possible to identify neo-antigens based on patientspecific gene mutations. Successful findings of immune checkpoint inhibitors (ICIs) in clinical trials have shed a light on tumor antigens which plays a key role so that they could be a candidate of novel therapeutic target. Since correlation between response to ICIs and neo-antigen has been clarified, it has become gradually clear that the immune response recognizing the neo-antigens plays a central role in anti-cancer immunity. Neo-antigens can elicit a strong immune response and are promising targets for novel cancer vaccine therapy or T-cell therapy, even though there are still some issues such as exhaustion and refractory state of T cells that they recognize. There are some types of tumor antigens with various specificity and immunogenicity to subject tumor. Several approaches utilizing tumor specific antigens are emerging as candidates of combination therapy together with ICI to maximize benefit from ICI treatment. Further studies of cancer antigens are expected to be the key to the next breakthrough in immunotherapy.
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肿瘤特异性抗原研究进展
是否存在被T细胞识别的“肿瘤抗原”一直存在争议,直到20世纪80年代,小鼠和人类的肿瘤抗原相继被鉴定出来。近年来,基因组测序技术的进步使得根据患者特异性基因突变鉴定新抗原成为可能。免疫检查点抑制剂(ICIs)在临床试验中的成功发现,揭示了肿瘤抗原的关键作用,使其成为新的治疗靶点。由于对ICIs的应答与新抗原之间的相关性已经被阐明,人们逐渐清楚地认识到,识别新抗原的免疫应答在抗癌免疫中起着核心作用。新抗原可以引起强烈的免疫反应,是新型癌症疫苗治疗或T细胞治疗的有希望的靶点,尽管它们识别的T细胞仍然存在一些问题,如衰竭和难治状态。肿瘤抗原对肿瘤具有不同的特异性和免疫原性。利用肿瘤特异性抗原的几种方法正在成为与ICI联合治疗的候选方法,以最大限度地从ICI治疗中获益。对癌症抗原的进一步研究有望成为免疫治疗下一个突破的关键。
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