武汉基于序列的重组抗原表达在E. 大肠杆菌引起的抗体能够与Omicron S-蛋白结合
Ekaterina Evtushenko1, Ekaterina Ryabchevskaya1, Angelina Kovalenko1
1Department of Virology, Faculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia.
International journal of molecular sciences
|August 29, 2024
概括
使用合成生物学开发的新型重组冠状病毒抗原有效诱导针对Omicron变异的抗体. 这些在细菌中产生的通用抗原对广泛的SARS-CoV-2疫苗有很大的前景.
科学领域:
- 疫苗学 疫苗学 疫苗学
- 免疫学 免疫学 免疫学
- 合成生物学 合成生物学
背景情况:
- 由于SARS-CoV-2的持续突变,因此需要开发通用冠状病毒疫苗.
- 设计针对多种变异的疫苗仍然是疫苗学中的一个重大挑战.
研究的目的:
- 评估先前开发的复合冠状病毒抗原与Omicron变种的交叉反应性.
- 评估与不同辅助剂配制的这些抗原的免疫性.
主要方法:
- 基于2019年武汉变种序列的重组抗原是在大肠杆菌细菌表达系统中产生的.
- 分析了抗体的产生和与Omicron变体的全长S蛋白的相互作用.
- 在小鼠中使用弗洛恩德辅助剂,Al(OH) 3和球形粒子 (SP) 辅助剂进行了免疫性研究.
主要成果:
- 重组抗原成功诱导了与Omicron变体的S蛋白交叉反应的抗体.
- 所有测试的辅助剂配方 (Freund,Al,OH3,SPs) 在小鼠中都刺激了显著的Omicron特异性IgG产生.
- 细菌表达系统被证明是适合生产抗原活性通用抗原的.
结论:
- 开发的通用冠状病毒抗原与像Omicron这样的SARS-CoV-2变种具有交叉反应性.
- 这些抗原是开发针对SARS-CoV-2的广谱疫苗的有希望的候选人.
- 合成生物学和细菌表达系统为制造有效的交叉反应疫苗提供了可行的策略.
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