Wang Rui, Wu Jingni, Lin Yifeng, Xiao Yufei, Yang Bin, Yao Sheng, Pan Tianhui, Fu Zhixuan, Li Shuyu, Wang Caihua, Zhu Yongliang
Laboratory of Gastroenterology, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Department of International Healthcare Center and General Medicine, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Cell Rep Med. 2025 Mar 18;6(3):101981. doi: 10.1016/j.xcrm.2025.101981. Epub 2025 Feb 24.
Antigenic peptide-based mRNA vaccines have been explored for immunotherapeutic use in various types of cancer because of their advantages in activating durable and specific immune responses. However, their role in modulating tumor metastasis is still unclear. Here, we identify a conserved linear epitope-based peptide, Ma3P, located in the proteolytic region of major histocompatibility complex (MHC) class I-related chain A (MICA) α3 and further design mCM10-L, an mRNA vaccine that encodes the carrier protein CRM197 and 10 tandem repeats of Ma3P. We demonstrate that vaccination with mCM10-L induces the production of specific antibodies that block MICA/B α1/2 shedding, activate CD8 T cells and natural killer (NK) cells, and significantly inhibit MICA/B tumor metastasis in mice. Furthermore, mCM10-L stimulation triggers the production of specific antibodies to promote MICA/B-mediated immune killing in an in-vitro-interacting human organoid model and humanized mice. Our results indicate the potential clinical application prospects of the mCM10-L vaccine.
基于抗原肽的mRNA疫苗因其在激活持久且特异性免疫反应方面的优势,已被探索用于各类癌症的免疫治疗。然而,它们在调节肿瘤转移中的作用仍不清楚。在此,我们鉴定出一种基于保守线性表位的肽段Ma3P,其位于主要组织相容性复合体(MHC)I类相关链A(MICA)α3的蛋白水解区域,并进一步设计了mCM10-L,这是一种编码载体蛋白CRM197和10个串联重复Ma3P的mRNA疫苗。我们证明,用mCM10-L进行疫苗接种可诱导产生特异性抗体,这些抗体可阻断MICA/B α1/2的脱落,激活CD8 T细胞和自然杀伤(NK)细胞,并显著抑制小鼠体内MICA/B肿瘤转移。此外,mCM10-L刺激在体外相互作用的人类类器官模型和人源化小鼠中触发产生特异性抗体,以促进MICA/B介导的免疫杀伤。我们的结果表明了mCM10-L疫苗潜在的临床应用前景。