2022年初来自印度的突破性感染血清靶向保守的隐性5类表位,以对抗SARS-CoV-2变体的免疫逃逸。

IF 4 2区 医学 Q2 VIROLOGY
Indrani Das Jana, Kawkab Kanjo, Subhanita Roy, Munmun Bhasin, Shatarupa Bhattacharya, Indranath Banerjee, Subhasis Jana, Arjun Chatterjee, Alok Kumar Chakrabarti, Suman Chakraborty, Budhaditya Mukherjee, Raghavan Varadarajan, Arindam Mondal
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引用次数: 0

摘要

在2019冠状病毒病(COVID-19)大流行期间,绝大多数表位作图研究都集中在高收入国家接种mrna疫苗人群的血清中。相比之下,我们报告了对2022年初印度突破性感染患者分离的164份血清样本的分析,这些患者接受了两剂ChAdOx病毒载体疫苗。筛选血清对野生型(WT)、Kappa、Delta和Omicron BA.1病毒的中和广度。利用电荷扫描诱变技术、酵母表面展示技术和下一代测序技术,选择具有最高中和宽度和效力的3种血清进行表位定位。绘制的血清主要针对最近发现的5类隐性表位,在较小程度上针对1类和4类表位。5类表位在所有严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)变异和大多数sarbecovirus中是完全保守的。基于这些观察,对另外26种血清进行了表征,所有血清都显示出广泛的中和活性,包括对XBB.1.5的中和活性。这与从接受多剂量原始和更新mRNA疫苗的个体血清中获得的结果形成对比,其中观察到XBB和后来的关注变体(VOCs)的中和受损。我们的研究表明,在高度暴露人群中接种两剂ChAdOx疫苗足以对新出现和即将出现的关注变体产生实质性的中和广度。这些数据突出了混合免疫在提供广泛保护方面的重要作用,并为未来预防快速变异病毒的疫苗战略提供了信息。重要性:在全球范围内实施2019冠状病毒病(COVID-19)疫苗以及同时出现的新型严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)变体已经形成了针对人群的体液免疫反应。虽然确定这种免疫反应的特征对于在人群水平上监测疾病进展非常重要,但也必须以新型疫苗和疗法的形式制定有效的对策。印度实施了全球第二大COVID-19疫苗接种计划,并遇到了大量疫苗接种后的“突破性”感染。从一组突破性感染患者中,我们确定了其血清对不同SARS-CoV-2变体表现出广泛中和免疫的个体。有趣的是,这些血清主要针对一种新的隐性表位,这在西方国家先前进行的人群水平研究中未被发现。这种罕见的隐性表位在所有SARS-CoV-2变体中保持保守,包括最近出现的变体,以及可能导致未来爆发的sars样冠状病毒,因此代表了未来疫苗的潜在目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early 2022 breakthrough infection sera from India target the conserved cryptic class 5 epitope to counteract immune escape by SARS-CoV-2 variants.

During the coronavirus disease 2019 (COVID-19) pandemic, the vast majority of epitope mapping studies have focused on sera from mRNA-vaccinated populations from high-income countries. In contrast, here, we report an analysis of 164 serum samples isolated from patients with breakthrough infection in India during early 2022 who received two doses of the ChAdOx viral vector vaccine. Sera were screened for neutralization breadth against wild-type (WT), Kappa, Delta, and Omicron BA.1 viruses. Three sera with the highest neutralization breadth and potency were selected for epitope mapping, using charged scanning mutagenesis coupled with yeast surface display and next-generation sequencing. The mapped sera primarily targeted the recently identified class 5 cryptic epitope and, to a lesser extent, the class 1 and class 4 epitopes. The class 5 epitope is completely conserved across all severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants and for most sarbecoviruses. Based on these observations, an additional 26 sera were characterized, and all showed a broad neutralizing activity, including against XBB.1.5. This is in contrast with the results obtained with the sera from individuals receiving multiple doses of original and updated mRNA vaccines, where impaired neutralization of XBB and later variants of concern (VOCs) were observed. Our study demonstrates that two doses of the ChAdOx vaccine in a highly exposed population were sufficient to drive substantial neutralization breadth against emerging and upcoming variants of concern. These data highlight the important role of hybrid immunity in conferring broad protection and inform future vaccine strategies to protect against rapidly mutating viruses.

Importance: Worldwide implementation of coronavirus disease 2019 (COVID-19) vaccines and the parallel emergence of newer severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants have shaped the humoral immune response in a population-specific manner. While characterizing this immune response is important for monitoring disease progression at the population level, it is also imperative for developing effective countermeasures in the form of novel vaccines and therapeutics. India has implemented the world's second largest COVID-19 vaccination drive and encountered a large number of post-vaccination "breakthrough" infections. From a cohort of patients with breakthrough infection, we identified individuals whose sera showed broadly neutralizing immunity against different SARS-CoV-2 variants. Interestingly, these sera primarily target a novel cryptic epitope, which was not identified in previous population-level studies conducted in Western countries. This rare cryptic epitope remains conserved across all SARS-CoV-2 variants, including recently emerged ones and for the SARS-like coronaviruses that may cause future outbreaks, thus representing a potential target for future vaccines.

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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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