Shin Hojeong, Kang Seounghun, Chae Se-Youl, Won Cheolhee, Min Dal-Hee
Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.
Institute of Biotherapeutics Convergence Technology, Lemonex Inc., Seoul 06683, Republic of Korea.
ACS Appl Mater Interfaces. 2023 Mar 13. doi: 10.1021/acsami.2c19526.
Cancer vaccine is one of the immunotherapeutic strategies aiming to effectively deliver cancer antigens to professional antigen-presenting cells such as dendritic cells (DCs), macrophages, and B cells to elicit a cancer-specific immune response. Despite the advantages of the cancer vaccine that can be applied to various cancer types, the clinical approach is limited due to the non-specific or adverse immune responses, stability, and safety issues. In this study, we report an injectable nanovaccine platform based on large-sized (∼350 nm) porous silica nanoparticles (PSNs). We found that large-sized PSNs, called PS3, facilitated the formation of an antigen supply depot at the site of injection so that a single injection of PSN-based nanovaccine elicited sufficient tumor-specific cell-mediated and humoral immune response. As a result, antigen-loaded PS3 induced successful tumor regression in prophylactic and therapeutic vaccination.
癌症疫苗是一种免疫治疗策略,旨在有效地将癌症抗原递呈给专职抗原呈递细胞,如树突状细胞(DCs)、巨噬细胞和B细胞,以引发癌症特异性免疫反应。尽管癌症疫苗具有可应用于多种癌症类型的优势,但由于非特异性或不良免疫反应、稳定性和安全性问题,其临床应用方法受到限制。在本研究中,我们报道了一种基于大尺寸(约350nm)多孔二氧化硅纳米颗粒(PSNs)的可注射纳米疫苗平台。我们发现,称为PS3的大尺寸PSNs促进了注射部位抗原供应库的形成,因此单次注射基于PSN的纳米疫苗可引发足够的肿瘤特异性细胞介导和体液免疫反应。结果,负载抗原的PS3在预防性和治疗性疫苗接种中均成功诱导了肿瘤消退。