S. Pongcharoen, Nongphanga Kaewsringam, Poorichaya Somaparn, S. Roytrakul, Y. Maneerat, Komsak Pintha, Supachai Topanurak
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引用次数: 0
摘要
癌症是导致全球死亡的主要原因,传统治疗方法痛苦、复杂,而且对健康细胞有负面影响。然而,癌症免疫疗法已成为一种前景广阔的替代疗法。癌症免疫疗法的原理是重新激活 T 细胞,以对抗主要组织相容性复合体(MHC)上的多肽抗原肿瘤。这些肽抗原是通过omics技术、蛋白质组学、基因组学和生物信息学来识别的,这就是免疫肽组学。事实上,免疫肽组学能鉴定出对癌症免疫疗法非常有用的新抗原。本综述探讨了免疫肽组学在各种免疫疗法中的应用,如基于肽的疫苗、免疫检查点抑制剂、溶瘤病毒和嵌合抗原受体T细胞。我们还讨论了新抗原的多样性如何使新型抗原肽的发现成为可能,同时翻译后修饰的肽如何使与 MHC 或所谓 MHC 配体组结合的整体肽多样化。免疫肽组学的发展与时俱进,非常活跃,尤其是在临床应用方面。免疫肽组学有望快速、准确、可靠地应用于癌症免疫疗法。
Cancer is the primary cause of death worldwide, and conventional treatments are painful, complicated, and have negative effects on healthy cells. However, cancer immunotherapy has emerged as a promising alternative. Principle of cancer immunotherapy is the re-activation of T-cell to combat the tumor that presents the peptide antigen on major histocompatibility complex (MHC). Those peptide antigens are identified with the set of omics technology, proteomics, genomics, and bioinformatics, which referred to immunopeptidomics. Indeed, immunopeptidomics can identify the neoantigens that are very useful for cancer immunotherapies. This review explored the use of immunopeptidomics for various immunotherapies, i.e., peptide-based vaccines, immune checkpoint inhibitors, oncolytic viruses, and chimeric antigen receptor T-cell. We also discussed how the diversity of neoantigens allows for the discovery of novel antigenic peptides while post-translationally modified peptides diversify the overall peptides binding to MHC or so-called MHC ligandome. The development of immunopeptidomics is keeping up-to-date and very active, particularly for clinical application. Immunopeptidomics is expected to be fast, accurate and reliable for the application for cancer immunotherapies.