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最终中和了威胁?一种新型 SARS-CoV-2 疫苗平台,可引发增强的中和抗体反应。

Finally neutralizing the threat? A novel SARS-CoV-2 vaccine platform that elicits enhanced neutralizing antibody responses.

机构信息

Department of Microbiology, Immunology, and Molecular Genetics, University of Texas Health Science Center, San Antonio, Texas, USA.

出版信息

mBio. 2024 Apr 10;15(4):e0006724. doi: 10.1128/mbio.00067-24. Epub 2024 Feb 26.

Abstract

The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) outbreak took the world by storm due to its rapid global spread and unpredictable disease outcomes. The extraordinary ascension of SARS-CoV-2 to pandemic status motivated a world-wide effort to rapidly develop vaccines that could effectively suppress virus spread and mitigate severe disease. These efforts culminated in the development and deployment of several highly effective vaccines that were heralded as the beginning-of-the-end of the pandemic. However, these successes were short lived due to the unexpected and continuous emergence of more transmissible and immune-evasive SARS-CoV-2 variants. Thus, attention has shifted toward developing novel vaccine platforms that elicit more robust and sustained neutralizing antibody responses. Recent findings by Muñoz-Alía and colleagues address this by combining a live recombinant measles vaccine platform with novel biochemical approaches to generate vaccine candidates that bolster the potency of neutralizing antibody responses against diverse SARS-CoV-2 spike proteins (M. Á. Muñoz-Alía, R. A. Nace, B. Balakrishnan, L. Zhang, et al., mBio 9:e02928-23, 2024, https://doi.org/10.1128/mbio.02928-23).

摘要

严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)的爆发因其迅速在全球范围内传播和不可预测的疾病结果而席卷全球。SARS-CoV-2 非凡地上升为大流行状态,促使全世界努力快速开发能够有效抑制病毒传播和减轻严重疾病的疫苗。这些努力最终促成了几种高度有效的疫苗的开发和部署,这些疫苗被视为大流行结束的开始。然而,由于不可预测的、持续出现的更具传染性和免疫逃避性的 SARS-CoV-2 变体,这些成功是短暂的。因此,人们的注意力已经转向开发新型疫苗平台,以引发更强大和持久的中和抗体反应。最近 Muñoz-Alía 及其同事的研究结果通过将活重组麻疹疫苗平台与新的生化方法相结合来解决这个问题,从而产生了增强针对多种 SARS-CoV-2 刺突蛋白的中和抗体反应效力的候选疫苗(M. Á. Muñoz-Alía、R. A. Nace、B. Balakrishnan、L. Zhang 等人,mBio 9:e02928-23, 2024, https://doi.org/10.1128/mbio.02928-23)。

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