mRNA vaccines have shown great efficacy against SARS-CoV-2, yet challenges remain in optimizing vaccine components to achieve enhanced immune response and vaccine stability. In this study, we developed CPVax-CoV, a new lyophilized mRNA vaccine that features novel thiolactone-based ionizable lipids and newly designed untranslated regions (UTRs) for enhanced expression. Incorporation of these optimized components into our vaccine candidate CPVax-CoV significantly improved immune responses in mice compared to commercially available mRNA vaccines. Moreover, lyophilized CPVax-CoV has proven to be thermostable, maintaining its biological activity for up to one year at 4â°C and 25â°C after lyophilization, overcoming the cold-chain limitations of current mRNA vaccines. This vaccine demonstrates protective efficacy against ancestral SARS-CoV-2 and the Omicron XBB variant, offering a scalable solution for global distribution and pandemic preparedness. These findings underscore the potential of this platform for future next-generation mRNA vaccine development.
Preserved efficacy of lyophilized SARS-CoV-2 mRNA vaccine incorporating novel ionizable lipids after one year at 25â°C.
含有新型可电离脂质的冻干SARS-CoV-2 mRNA疫苗在25℃下保存一年后仍保持其效力
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作者:Mata Elena, Broset Esther, Matute Carlos, Stoian Andrei, Adame Susana, Alejo Teresa, López Alexandre, Andrés Beatriz, Heredero Juan, de Miguel Diego, Giménez-Warren Javier, Lampaya Verónica, Casabona Diego, Calvo Alba, Quincoces Gema, Peñuelas Iván, Gamazo Carlos, Uranga Iratxe, Peña Natacha, Arias Maykel, Pardo Julián, Moreno Bernardino, Badiola Juan, MartÃnez-Oliván Juan, Pérez-Herrán Esther
| 期刊: | NPJ Vaccines | 影响因子: | 6.500 |
| 时间: | 2025 | 起止号: | 2025 Jul 1; 10(1):135 |
| doi: | 10.1038/s41541-025-01201-1 | 研究方向: | 炎症/感染 |
| 疾病类型: | 新冠 | ||
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