长时间的Omicron特异性B细胞成熟缓解了由SARS-CoV-2无活化疫苗诱导的免疫印记
Ayijiang Yisimayi1,2, Weiliang Song1,2, Jing Wang1,2
1Biomedical Pioneering Innovation Center (BIOPIC), School of Life Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing, People's Republic of China.
Emerging microbes & infections
|October 3, 2024
概括
由于免疫印记,SARS-CoV-2疫苗更新面临挑战. 与mRNA疫苗不同,Omicron感染可以通过增强Omicron特异性记忆B细胞来克服非活化疫苗的印记.
科学领域:
- 免疫学 免疫学 免疫学
- 病毒学 病毒学
- 疫苗学 疫苗学 疫苗学
背景情况:
- 来自祖先菌株的SARS-CoV-2免疫印记使新变种的疫苗更新复杂化.
- 之前的研究表明,Omicron暴露可以覆盖非活化疫苗印记,但不能覆盖mRNA疫苗印记.
研究的目的:
- 调查通过Omicron变种突破性感染 (BTI) 后,无活化疫苗 (CoronaVac) 接种者免疫印记的缓解.
- 了解在Omicron暴露后的非活化和mRNA疫苗平台之间免疫印记的差异.
主要方法:
- 在BA.5/BF.7突破感染后接种CoronaVac疫苗的个体中分析免疫印记.
- 在长时间内对Omicron特异性记忆B细胞 (MBCs) 和抗体特征进行量化.
主要成果:
- 在CoronaVac接种者中,在Omicron BTI后观察到Omicron特定MBC的显著增加.
- 抗体显示出增强的体质突变和中和功效.
- 感染后的MBC表皮质分布与未接种疫苗的个体相似,表明缓解了印记.
结论:
- 在最初的Omicron暴露期间,Omicron特定的天真B细胞的激活和扩张有助于缓解CoronaVac诱导的免疫印记.
- 这一过程的缺失可能解释了mRNA疫苗接种者的持续性免疫印记.
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