Department of Ultrasound, Institute of Ultrasound in Medicine and Engineering, Zhongshan Hospital, Fudan University, Shanghai, 200032, P. R. China.
Department of Medical Ultrasound, Center of Minimally Invasive Treatment for Tumor, Shanghai Tenth People's Hospital, Ultrasound Research and Education Institute, Clinical Research Center for Interventional Medicine, School of Medicine, Tongji University. Shanghai 200072, P. R. China.
Adv Sci (Weinh). 2024 Jul;11(28):e2307225. doi: 10.1002/advs.202307225. Epub 2024 May 14.
Therapeutic mRNA vaccines have become powerful therapeutic tools for severe diseases, including infectious diseases and malignant neoplasms. mRNA vaccines encoding tumor-associated antigens provide unprecedented hope for many immunotherapies that have hit the bottleneck. However, the application of mRNA vaccines is limited because of biological instability, innate immunogenicity, and ineffective delivery in vivo. This study aims to construct a novel mRNA vaccine delivery nanosystem to successfully co-deliver a tumor-associated antigen (TAA) encoded by the Wilms' tumor 1 (WT1) mRNA. In this system, named PSB@NbC/mRNA, photosynthetic bacteria (PSB) efficiently delivers the iMXene-WT1 mRNA to the core tumor region using photo-driven and hypoxia-driven properties. The excellent photothermal therapeutic (PTT) properties of PSB and 2D iMxene (NbC) trigger tumor immunogenic cell death, which boosts the release of the WT1 mRNA. The released WT1 mRNA is translated, presenting the TAA and amplifying immune effect in vivo. The designed therapeutic strategy demonstrates an excellent ability to inhibit distant tumors and counteract postsurgical lung metastasis. Thus, this study provides an innovative and effective paradigm for tumor immunotherapy, i.e., photo-immunogene cancer therapy, and establishes an efficient delivery platform for mRNA vaccines, thereby opening a new path for the wide application of mRNA vaccines.
治疗性 mRNA 疫苗已成为治疗严重疾病(包括传染病和恶性肿瘤)的有力治疗工具。编码肿瘤相关抗原的 mRNA 疫苗为许多免疫疗法提供了前所未有的希望,这些疗法已经遇到了瓶颈。然而,由于生物不稳定性、固有免疫原性和体内无效传递,mRNA 疫苗的应用受到限制。本研究旨在构建一种新型的 mRNA 疫苗传递纳米系统,成功共递Wilms 瘤 1(WT1)mRNA 编码的肿瘤相关抗原(TAA)。在该系统中,命名为 PSB@NbC/mRNA,光合细菌(PSB)利用光驱动和缺氧驱动特性,将 iMXene-WT1 mRNA 有效递送至核心肿瘤区域。PSB 和 2D iMxene(NbC)的优异光热治疗(PTT)性能触发肿瘤免疫原性细胞死亡,从而促进 WT1 mRNA 的释放。释放的 WT1 mRNA 被翻译,在体内呈现 TAA 并放大免疫效应。所设计的治疗策略表现出抑制远处肿瘤和对抗手术后肺转移的优异能力。因此,本研究为肿瘤免疫治疗提供了一种创新且有效的范例,即光免疫基因癌症治疗,并为 mRNA 疫苗建立了有效的传递平台,从而为 mRNA 疫苗的广泛应用开辟了新途径。