SARS-CoV-2组克隆XBB.1.5亚谱系的研究进展

A. Yameny
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引用次数: 0

摘要

2019冠状病毒病大流行的特征是高度传染性的严重急性呼吸综合征冠状病毒2 (SARS-CoV-2), Omicron变体,首次在博茨瓦纳报告,并于2022年初在全球范围内迅速传播,2023年初带来了SARS-CoV-2的Omicron变体的新亚变体,称为xbb1.5。Omicron XBB.1.5亚变体是XBB变体的一个亚谱系,XBB变体是两个BA.2亚谱系的重组,具有额外的刺突受体结合域(RBD)变化,S486P。利用伪病毒中和实验证明,XBB.1.5与XBB.1一样具有免疫逃避性,XBB.1是迄今为止具有最大免疫逃避性的Omicron亚变体。目前还没有关于疫苗对严重疾病或死亡的实际有效性的数据。此时,没有迹象表明XBB.1.5的感染严重程度与早期传播的欧米克隆亚系不同。COVID-19诊断的金标准是使用上呼吸道拭子或唾液进行逆转录-定量聚合酶链反应(RT-qPCR)检测。目前还没有对XBB.1.5的疫苗有效性(VE)估计,也没有关于COVID-19抗病毒疗法有效性的具体数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of SARS-CoV-2 Omicron XBB.1.5 sub-lineage: A review
The COVID-19 pandemic is characterized by the highly infectious severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Omicron variant, which was first reported in Botswana and quickly spread as the dominant variant worldwide during early 2022, the start of 2023 brings a new subvariant of the Omicron variant of SARS-CoV-2, known as XBB.1.5. The Omicron XBB.1.5 subvariant is a sublineage of the XBB variant, a recombinant of two BA.2 sublineages, with an additional spike receptor-binding domain (RBD) change, S486P. It is demonstrated that XBB.1.5 is just as immunologically evasive as XBB.1, the Omicron subvariant with the largest immune escape to date, using pseudotyped viral neutralization experiments. There is currently no data on real-world vaccine effectiveness against severe disease or death. At this time, there are no indications that XBB.1.5's infection severity differs from that of earlier Omicron sub-lineages that were circulating. The gold standard for COVID-19 diagnosis is reverse transcription-quantitative polymerase chain reaction (RT-qPCR) testing using upper respiratory tract swabs or saliva. there are no vaccine effectiveness (VE) estimates for XBB.1.5 yet, no specific data are currently available on the effectiveness of COVID-19 antiviral therapeutics.
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