编码保存的非尖端抗原的T细胞导向疫苗BNT162b4可以保护动物免受严重的SARS-CoV-2感染
Christina M Arieta1, Yushu Joy Xie1, Daniel A Rothenberg1
1BioNTech US, 40 Erie Street, Cambridge, MA 02139, USA.
Cell
|May 10, 2023
概括
一种新的疫苗成分BNT162b4增强了对SARS-CoV-2变种的T细胞免疫力. 结合现有疫苗,它减少了动物模型中的疾病严重性和病毒载荷,为未来的COVID-19保护提供了希望.
科学领域:
- 免疫学
- 疫苗学
- 病毒学
背景情况:
- 对于抗击SARS-CoV-2等β型冠状病毒感染,T细胞反应至关重要,与COVID-19的严重程度降低相关.
- SARS-CoV-2 变种对现有的疫苗诱导免疫力构成挑战.
- 针对保存的病毒表位可以扩大疫苗对进化变异的有效性.
研究的目的:
- 设计和评估针对保存的SARS-CoV-2表位的mRNA疫苗组件BNT162b4.
- 评估单独使用和与BNT162b2结合使用的BNT162b4的免疫性和保护性.
- 调查BNT162b4对SARS-CoV-2变种提供广泛保护的潜力.
主要方法:
- BNT162b4 设计用于编码SARS-CoV-2 核体,膜和ORF1ab 蛋白质的变异性保存部分.
- 通过测量动物模型中的多功能CD4+和CD8+T细胞反应来评估免疫性.
- 通过使用病毒变体,评估疾病严重程度和病毒标位,通过对子进行挑战研究来评估疗效.
主要成果:
- 在动物模型中,BNT162b4诱导多功能T细胞对多种表位的反应.
- 与BNT162b2的同时使用引起T细胞反应,同时保持突起特异性免疫力.
- 在感染SARS-CoV-2变种的仓鼠中,BNT162b4显示出对严重疾病的保护,并降低了病毒标位.
结论:
- 包括BNT162b4和BNT162b2在内的组合疫苗可以减少COVID-19的严重程度和持续时间,而不是当前和未来的变种.
- BNT162b4对增强T细胞介导的针对SARS-CoV-2的免疫力具有前景.
- 目前正在对BNT162b4与更新的双价疫苗进行临床评估.
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