Division of Abdominal Tumor Multimodality Treatment, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Front Immunol. 2024 Jul 11;15:1437774. doi: 10.3389/fimmu.2024.1437774. eCollection 2024.
Alternative splicing (AS) functions as a crucial program in transcriptional modulation, leading to proteomic diversity and functional alterations of proteins. These splicing actions induce various neoantigens that hold prognostic significance and contribute to various aspects of cancer progression, including immune responses against cancer. The advent of immunotherapy has remarkably revolutionized tumor therapy. In this regard, AS-derived neoantigens are potent targets for cancer vaccines and chimeric antigen receptor (CAR) T cell therapies. In this review, we outline that AS-derived neoantigens serve as promising immunotherapeutic targets and guide immunotherapy strategies. This evidence contributes to a deeper comprehension of the complexity of proteomic diversity and provides novel perspectives and techniques for precision medicine in immunotherapy. Moreover, we underscore the obstacles that are awaited to be addressed for this novel approach to become clinically applicable.
可变剪接(AS)作为转录调控的关键程序,导致蛋白质的蛋白质组多样性和功能改变。这些剪接作用诱导具有预后意义的各种新抗原,并有助于癌症进展的各个方面,包括针对癌症的免疫反应。免疫疗法的出现极大地改变了肿瘤治疗。在这方面,AS 衍生的新抗原是癌症疫苗和嵌合抗原受体(CAR)T 细胞疗法的有效靶点。在这篇综述中,我们概述了 AS 衍生的新抗原作为有前途的免疫治疗靶点,并指导免疫治疗策略。这一证据有助于更深入地了解蛋白质组多样性的复杂性,并为免疫治疗中的精准医学提供新的观点和技术。此外,我们强调了为使这种新方法具有临床应用价值而有待解决的障碍。