Tumor neoantigens: Novel strategies for application of cancer immunotherapy

被引:13
作者
Guan, Hanyang [1 ]
Wu, Yue [2 ]
Li, Lu [3 ]
Yang, Yabing [1 ]
Qiu, Shenghui [1 ]
Zhao, Zhan [1 ]
Chu, Xiaodong [1 ]
He, Jiashuai [1 ]
Chen, Zuyang [1 ]
Zhang, Yiran [1 ]
Ding, Hui [1 ]
Pan, Jinghua [1 ]
Pan, Yunlong [1 ]
机构
[1] Jinan Univ, Dept Gen Surg, Affiliated Hosp 1, Guangzhou 510632, Peoples R China
[2] Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Dept Gynecol, Womens Hosp, Nanjing 210004, Peoples R China
[3] Jinan Univ, Dept Gastroenterol, Affiliated Hosp 1, Guangzhou 510630, Peoples R China
关键词
Immunotherapy; Tumor vaccine; Adoptive T cell therapy; Chimeric antigen receptor; T-CELL RESPONSES; MHC CLASS-I; MUTATIONAL BURDEN; VACCINE; CHALLENGES; IMMUNOGENICITY; ASSOCIATION; PERSPECTIVE; PREDICTION; BIOMARKER;
D O I
10.32604/or.2023.029924
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Neoantigen-targeted immunotherapy is a rapidly advancing field that holds great promise for treating cancer. The recognition of antigens by immune cells is a crucial step in tumor-specific killing, and neoantigens generated by mutations in cancer cells possess high immunogenicity and are selectively expressed in tumor cells, making them an attractive therapeutic target. Currently, neoantigens find utility in various domains, primarily in the realm of neoantigen vaccines such as DC vaccines, nucleic acid vaccines, and synthetic long peptide vaccines. Additionally, they hold promise in adoptive cell therapy, encompassing tumor-infiltrating cells, T cell receptors, and chimeric antigen receptors which are expressed by genetically modified T cells. In this review, we summarized recent progress in the clinical use of tumor vaccines and adoptive cell therapy targeting neoantigens, discussed the potential of neoantigen burden as an immune checkpoint in clinical settings. With the aid of state-of-the-art sequencing and bioinformatics technologies, together with significant advancements in artificial intelligence, we anticipated that neoantigens will be fully exploited for personalized tumor immunotherapy, from screening to clinical application.
引用
收藏
页码:437 / 448
页数:12
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