Key Laboratory of Tropical Translational Medicine of Ministry of Education & Hainan Provincial Key Laboratory of Tropical Medicine, Hainan Medical University, Haikou 571199, PR China; State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, PR China.
Key Laboratory of Tropical Translational Medicine of Ministry of Education & Hainan Provincial Key Laboratory of Tropical Medicine, Hainan Medical University, Haikou 571199, PR China.
J Control Release. 2021 Apr 10;332:245-259. doi: 10.1016/j.jconrel.2021.02.029. Epub 2021 Feb 27.
Virus is a nanosized pathogen and mainly composed of viral protein and nucleic acids. Under the pressure of long-term selection, mammals have gradually evolved effective immune mechanisms to defend themselves against viruses. In addition to recognizing viral proteins, immune system can also respond to viral sequence-specific nucleic acids, including CpG ODN, single- and double- strand RNA, and thereby enhancing the ability to remove infected viruses. Inspired by these immune mechanisms, we have attempted to develop a tracing virus-mimicking nanovaccine for tumor immunotherapy. This nanovaccine mainly consists of nucleic acids (CpG ODN), proteins (including tumor-associated antigen, and neutravidin (nAvidin) as skeleton materials for constructing nanovaccine and carriers for loading tumor-associated antigen and CpG ODN), and the dye molecules for assembling nAvidin to form nanoparticles comparable in size to viruses and tracing the vaccine in vitro and in vivo. The as-prepared nanovaccine efficiently induces the maturation of dendritic cell, the enhancement of antigen cross-presentation ability, and amplification of cytokine production in vitro. Furthermore, in vivo analysis clearly shows that it targets lymph nodes, successfully presents antigens to generate tumor-antigen-specific CD8 T cells and induces a Th1-biased immune response. Most notably, this virus-mimicking nanovaccine significantly inhibits the growth of antigen-expressed tumor and prolongs the survival time of the antigen-expressed tumor bearing mice.
病毒是一种纳米级病原体,主要由病毒蛋白和核酸组成。在长期选择压力下,哺乳动物逐渐进化出有效的免疫机制来抵御病毒。除了识别病毒蛋白外,免疫系统还可以对病毒序列特异性核酸(包括 CpG ODN、单链和双链 RNA)产生反应,从而增强清除感染病毒的能力。受这些免疫机制的启发,我们尝试开发了一种模拟病毒的跟踪纳米疫苗用于肿瘤免疫治疗。该纳米疫苗主要由核酸(CpG ODN)、蛋白质(包括肿瘤相关抗原和链亲和素(nAvidin)作为构建纳米疫苗的骨架材料和负载肿瘤相关抗原和 CpG ODN 的载体)以及用于组装 nAvidin 以形成与病毒大小相当的纳米颗粒并在体外和体内追踪疫苗的染料分子组成。所制备的纳米疫苗在体外有效地诱导树突状细胞成熟、增强抗原交叉呈递能力和细胞因子产生的放大。此外,体内分析清楚地表明,它靶向淋巴结,成功地呈递抗原以产生肿瘤抗原特异性 CD8 T 细胞,并诱导 Th1 偏向性免疫反应。值得注意的是,这种模拟病毒的纳米疫苗显著抑制了表达抗原的肿瘤的生长并延长了表达抗原的肿瘤荷瘤小鼠的存活时间。