Wang Liuyang, Lin Xuan, Sheng Yanan, Zhu Hongyu, Li Zhengjun, Su Zhiguo, Yu Rong, Zhang Songping
Key Laboratory of Drug-Targeting and Drug Delivery System of the Ministry of Education, West China School of Pharmacy, Sichuan University Chengdu 610041 China
State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences Beijing 100190 China
Nanoscale Adv. 2023 Feb 7;5(5):1433-1449. doi: 10.1039/d2na00767c. eCollection 2023 Feb 28.
Encapsulating antigens with zeolitic imidazole framework-8 (ZIF-8) exhibits many advantages in vaccine development. However, most viral antigens with complex particulate structures are sensitive to pH or ionic strength, which cannot tolerate harsh synthesis conditions of ZIF-8. Balancing the viral integrity and the growth of ZIF-8 crystals is crucial for the successful encapsulation of these environment-sensitive antigens in ZIF-8. Here, we explored the synthesis of ZIF-8 on inactivated foot and mouth disease virus (known as 146S), which is easily disassociated into no immunogenic subunits under the existing ZIF-8 synthesis conditions. Our results showed that intact 146S could be encapsulated into ZIF-8 with high embedding efficiency by lowering the pH of the 2-MIM solution to 9.0. The size and morphology of 146S@ZIF-8 could be further optimized by increasing the amount of Zn or adding cetyltrimethylammonium bromide (CTAB). 146S@ZIF-8 with a uniform diameter of about 49 nm could be synthesized by adding 0.01% CTAB, which was speculated to be composed of single 146S armored with nanometer-scale ZIF-8 crystal networks. Plenty of histidine on the 146S surface forms a unique His-Zn-MIM coordination in the near vicinity of 146S particles, which greatly increases the thermostability of 146S by about 5 °C, and the nano-scale ZIF-8 crystal coating exhibited extraordinary stability to resist EDTE-treatment. More importantly, the well-controlled size and morphology enabled 146S@ZIF-8(0.01% CTAB) to facilitate antigen uptake. The immunization of 146S@ZIF-8(4×Zn) or 146S@ZIF-8(0.01% CTAB) significantly enhanced the specific antibody titers and promoted the differentiation of memory T cells without adding another immunopotentiator. This study reported for the first time the strategy of the synthesis of crystalline ZIF-8 on an environment-sensitive antigen and demonstrated that the nano-size and appropriate morphology of ZIF-8 are crucial to exert adjuvant effects, thus expanding the application of MOFs in vaccine delivery.
用沸石咪唑框架-8(ZIF-8)包裹抗原在疫苗开发中具有许多优势。然而,大多数具有复杂颗粒结构的病毒抗原对pH值或离子强度敏感,无法耐受ZIF-8苛刻的合成条件。平衡病毒完整性和ZIF-8晶体生长对于在ZIF-8中成功包裹这些环境敏感抗原至关重要。在此,我们探索了在灭活口蹄疫病毒(称为146S)上合成ZIF-8,在现有的ZIF-8合成条件下,146S很容易解离成无免疫原性的亚基。我们的结果表明,通过将2-甲基咪唑溶液的pH值降至9.0,完整的146S可以以高包埋效率包裹在ZIF-8中。通过增加锌的量或添加十六烷基三甲基溴化铵(CTAB),可以进一步优化146S@ZIF-8的尺寸和形态。添加0.01% CTAB可以合成直径约49 nm的均匀146S@ZIF-8,推测其由包裹有纳米级ZIF-8晶体网络的单个146S组成。146S表面大量的组氨酸在146S颗粒附近形成独特的His-Zn-MIM配位,使146S的热稳定性大大提高约5℃,纳米级ZIF-8晶体涂层表现出非凡的稳定性以抵抗EDTA处理。更重要的是,良好控制的尺寸和形态使146S@ZIF-8(0.01% CTAB)便于抗原摄取。在不添加其他免疫增强剂的情况下,用146S@ZIF-8(4×Zn)或146S@ZIF-8(0.01% CTAB)免疫可显著提高特异性抗体滴度并促进记忆T细胞分化。本研究首次报道了在环境敏感抗原上合成结晶ZIF-8的策略,并证明ZIF-8的纳米尺寸和合适形态对于发挥佐剂作用至关重要,从而扩大了金属有机框架在疫苗递送中的应用。