CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Computation strategies and clinical applications in neoantigen discovery towards precision cancer immunotherapy.
Computation strategies and clinical applications in neoantigen discovery towards precision cancer immunotherapy.
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新抗原是由恶性细胞产生的肿瘤特异性肽,可呈递给T细胞以引发免疫反应。由于其肿瘤特异性特征,新抗原已成为癌症免疫治疗中最有前景的生物标志物和靶点之一。既往研究已证明其能够介导肿瘤特异性免疫反应,靶向并消除肿瘤细胞,同时保留正常细胞功能。在高通量测序技术、质谱分析和人工智能进步的推动下,研究人员对建立更准确的新抗原预测算法的兴趣日益增长。在此,我们对整合性新抗原预测算法进行了全面综述,涵盖任务定义、理论发展、基准数据集、前沿应用和未来研究方向。我们系统评估了新抗原来源表征和预测算法的最新进展,特别关注为HLA-肽结合和TCR识别开发的创新方法。此外,我们探讨了新抗原在个性化癌症疫苗设计和过继性细胞治疗中的前沿应用。我们描述了基于新抗原治疗的潜在研究方向和未来前景,包括整合多组学数据以发现通用新抗原、解决算法泛化挑战以及多样化新抗原验证方法。
Neoantigens, which are tumor-specific peptides generated by malignant cells, can be presented to T cells to elicit immune responses. Owing to their tumor-specific properties, neoantigens have emerged as one of the most promising biomarkers and targets for cancer immunotherapy.
Previous studies have demonstrated their capacity to mediate tumor-specific immune responses in targeting and eliminating tumor cells while preserving normal cellular function. Driven by advancements in high-throughput sequencing technologies, mass spectrometry, and artificial intelligence, researchers have developed a growing interest in establishing more accurate neoantigen prediction algorithms.
Here, we presented a comprehensive review of integrated neoantigen prediction algorithms, encompassing task definition, theoretical developments, benchmark datasets, cutting-edge applications, and future research directions.
We systematically evaluated recent advancements in neoantigen source characterization and prediction algorithms, with particular emphasis on innovative methods for HLA-peptide binding and TCR recognition developed.
Additionally, we explored the cutting-edge applications of neoantigens in personalized cancer vaccine design and adoptive cell therapies.
We delineated potential research directions and the future prospects for neoantigen-based therapies, including integrating multi-omics data to discover universal neoantigens, addressing algorithmic generalization challenges and diversifying neoantigen validation methods.
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