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高活性的 ACE2 诱饵亲和力成熟体对奥密克戎 SARS-CoV-2 和新出现的冠状病毒的抑制作用。

High activity of an affinity-matured ACE2 decoy against Omicron SARS-CoV-2 and pre-emergent coronaviruses.

机构信息

Gene Therapy Program, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States of America.

出版信息

PLoS One. 2022 Aug 25;17(8):e0271359. doi: 10.1371/journal.pone.0271359. eCollection 2022.

Abstract

The viral genome of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), particularly its cell-binding spike protein gene, has undergone rapid evolution during the coronavirus disease 2019 (COVID-19) pandemic. Variants including Omicron BA.1 and Omicron BA.2 now seriously threaten the efficacy of therapeutic monoclonal antibodies and vaccines that target the spike protein. Viral evolution over a much longer timescale has generated a wide range of genetically distinct sarbecoviruses in animal populations, including the pandemic viruses SARS-CoV-2 and SARS-CoV-1. The genetic diversity and widespread zoonotic potential of this group complicates current attempts to develop drugs in preparation for the next sarbecovirus pandemic. Receptor-based decoy inhibitors can target a wide range of viral strains with a common receptor and may have intrinsic resistance to escape mutant generation and antigenic drift. We previously generated an affinity-matured decoy inhibitor based on the receptor target of the SARS-CoV-2 spike protein, angiotensin-converting enzyme 2 (ACE2), and deployed it in a recombinant adeno-associated virus vector (rAAV) for intranasal delivery and passive prophylaxis against COVID-19. Here, we demonstrate the exceptional binding and neutralizing potency of this ACE2 decoy against SARS-CoV-2 variants including Omicron BA.1 and Omicron BA.2. Tight decoy binding tracks with human ACE2 binding of viral spike receptor-binding domains across diverse clades of coronaviruses. Furthermore, in a coronavirus that cannot bind human ACE2, a variant that acquired human ACE2 binding was bound by the decoy with nanomolar affinity. Considering these results, we discuss a strategy of decoy-based treatment and passive protection to mitigate the ongoing COVID-19 pandemic and future airway virus threats.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的病毒基因组,特别是其细胞结合刺突蛋白基因,在 2019 年冠状病毒病(COVID-19)大流行期间经历了快速进化。包括奥密克戎 BA.1 和奥密克戎 BA.2 在内的变体现在严重威胁到针对刺突蛋白的治疗性单克隆抗体和疫苗的疗效。在更长的时间尺度上,病毒进化产生了广泛的遗传上不同的沙贝冠状病毒,包括大流行病毒 SARS-CoV-2 和 SARS-CoV-1。该组的遗传多样性和广泛的人畜共患潜力使得当前开发药物以应对下一次沙贝冠状病毒大流行的努力变得复杂。基于受体的诱饵抑制剂可以针对具有共同受体的广泛病毒株,并可能具有内在的抗逃逸突变和抗原漂移的能力。我们之前基于 SARS-CoV-2 刺突蛋白的受体靶标血管紧张素转换酶 2(ACE2)生成了一种亲和力成熟的诱饵抑制剂,并将其部署在重组腺相关病毒载体(rAAV)中,用于鼻内递送和被动预防 COVID-19。在这里,我们证明了这种 ACE2 诱饵对包括奥密克戎 BA.1 和奥密克戎 BA.2 在内的 SARS-CoV-2 变体的卓越结合和中和效力。紧密的诱饵结合与人类 ACE2 结合追踪了跨越冠状病毒不同进化枝的病毒刺突受体结合域。此外,在一种不能结合人类 ACE2 的冠状病毒中,获得人类 ACE2 结合能力的变体被诱饵以纳摩尔亲和力结合。考虑到这些结果,我们讨论了一种基于诱饵的治疗和被动保护策略,以减轻当前的 COVID-19 大流行和未来的气道病毒威胁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d48/9409550/e9232a36038b/pone.0271359.g001.jpg

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