牛痘
病毒学
接种疫苗
免疫
免疫
加药
病毒
效价
体内
医学
抗体
重组DNA
中和抗体
免疫学
病毒载体
免疫系统
斑块形成单元
重组病毒
临床前试验
生物
改良安卡拉痘苗
抗体效价
体液免疫
离体
免疫球蛋白G
免疫原性
特异性抗体
正痘病毒
作者
Kotaro Shobayashi,Jongho PARK,Hoshimi Aoyagi,Fumihiko Yasui,Michinori Kohara,Beomjoon Kim
标识
DOI:10.1038/s41598-025-29183-z
摘要
Recent advances in microneedle array patch (MAP) technology have highlighted its potential for efficient and accessible vaccine delivery. In this study, we developed a pillar-guided MAP (PG-MAP) loaded with a recombinant vaccinia virus (r-DIs-S) expressing the SARS-CoV-2 spike (S) gene. Our fabrication method enabled precise localization of a high viral titer (> 9.4 ± 1.8 × 10⁶ PFU per patch), as verified by plaque assay. In vivo immunization in mice demonstrated that the r-DIs-S-loaded PG-MAP elicited robust S-protein-specific IgG and neutralizing antibody responses. Upon SARS-CoV-2 challenge, all PG-MAP-immunized mice survived and maintained their body weight, whereas the control groups experienced severe results. These results demonstrated that the PG-MAP platform enables precise dosing, maintains viral stability, and induces potent protective immunity, offering a promising alternative for decentralized, minimally invasive vaccination strategies against emerging infectious diseases.
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