致病性,病毒学特征和SARS-CoV-2 JN.1衍生变体的免疫逃避,包括JN.1.7,KP.2,KP.3和KP.3.1.1
Jialu Shi1, Xiaoyu Zhao2,3, Xiaohui Jin4
1State Key Laboratory of Emerging Infectious Diseases, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, and Pandemics Research Alliance Unit at The University of Hong Kong, Hong Kong Special Administrative Region, China.
Nature communications
|December 11, 2025
概括
新型的KP.3.1.1 SARS-CoV-2变种显示,由于其S31del尖端突变,免疫逃避和病毒进入增加. 然而,它的致病性与其他变体相比较,突出显示了复杂的病毒进化.
科学领域:
- 病毒学 病毒学
- 免疫学 免疫学 免疫学
- 结构生物学 结构生物学
背景情况:
- KP.3.1.1 成为一种主要的SARS-CoV-2变种,继承了JN.1.
- 了解KP.3.1.1的病原和病毒学特征至关重要.
研究的目的:
- 综合评估KP.3.1.1.1.的病原和特征.
- 将KP.3.1.1与JN.1及其衍生品 (JN.1.7,KP.2,KP.3) 进行比较.
主要方法:
- 病毒变异的比较分析.
- 尖峰突变的结构分析.
- 伪病毒进入效率测试.
- 在仓鼠模型中对病原性进行评估.
主要成果:
- 在KP.3.1.1的尖端蛋白中的S31del突变增强了免疫逃避,并减少了康复血清的中和.
- S31del创建新的糖化位点,帮助抗体逃避,增加伪病毒进入效率.
- KP.3.1.1表现出类似于JN.1和KP.3的病原性,但在子中比JN.1.7和KP.2更高.
- NSP10 S33C突变抵消了S31del.所赋予的传染性增加.
结论:
- 一个单一的尖峰突变 (S31del) 可以驱动免疫逃生和增加病毒感染力.
- 尖峰和非尖峰突变之间的相互作用影响病毒适应性和进化.
- 冠状病毒表现出显著的进化可塑性.
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