Peltonen Karita, Feola Sara, Umer Husen M, Chiaro Jacopo, Mermelekas Georgios, Ylösmäki Erkko, Pesonen Sari, Branca Rui M M, Lehtiö Janne, Cerullo Vincenzo
Drug Research Program, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, 00790 Helsinki, Finland.
Helsinki Institute of Life Science (HiLIFE), University of Helsinki, 00790 Helsinki, Finland.
Cancers (Basel). 2021 Jul 7;13(14):3408. doi: 10.3390/cancers13143408.
Knowledge of clinically targetable tumor antigens is becoming vital for broader design and utility of therapeutic cancer vaccines. This information is obtained reliably by directly interrogating the MHC-I presented peptide ligands, the immunopeptidome, with state-of-the-art mass spectrometry. Our manuscript describes direct identification of novel tumor antigens for an aggressive triple-negative breast cancer model. Immunopeptidome profiling revealed 2481 unique antigens, among them a novel ERV antigen originating from an endogenous retrovirus element. The clinical benefit and tumor control potential of the identified tumor antigens and ERV antigen were studied in a preclinical model using two vaccine platforms and therapeutic settings. Prominent control of established tumors was achieved using an oncolytic adenovirus platform designed for flexible and specific tumor targeting, namely PeptiCRAd. Our study presents a pipeline integrating immunopeptidome analysis-driven antigen discovery with a therapeutic cancer vaccine platform for improved personalized oncolytic immunotherapy.
了解临床上可靶向的肿瘤抗原对于治疗性癌症疫苗的更广泛设计和应用至关重要。通过使用最先进的质谱技术直接检测MHC-I呈递的肽配体(免疫肽组),可以可靠地获得这些信息。我们的手稿描述了在侵袭性三阴性乳腺癌模型中新型肿瘤抗原的直接鉴定。免疫肽组分析揭示了2481种独特的抗原,其中一种源自内源性逆转录病毒元件的新型ERV抗原。在临床前模型中,使用两种疫苗平台和治疗设置研究了所鉴定的肿瘤抗原和ERV抗原的临床益处和肿瘤控制潜力。使用专为灵活和特异性肿瘤靶向设计的溶瘤腺病毒平台(即PeptiCRAd),实现了对已建立肿瘤的显著控制。我们的研究提出了一种将免疫肽组分析驱动的抗原发现与治疗性癌症疫苗平台相结合的流程,以改进个性化溶瘤免疫疗法。