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一种源自原始新冠病毒感染的人类抗体可有效中和奥密克戎毒株。

A human antibody derived from original SARS-CoV-2 infection effectively neutralizes omicron.

作者信息

Li Tingting, Zhou Bingjie, Dong Haoyu, Lavillette Dimitri, Li Dianfan

机构信息

Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200030, China.

Shanghai Institute of Immunity and Infection, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200030, China.

出版信息

Adv Biotechnol (Singap). 2024 Jan 29;2(1):2. doi: 10.1007/s44307-024-00011-1.

Abstract

SARS-CoV-2 (Severe acute respiratory syndrome coronavirus 2) Variants of Concern (VOCs), such as the Omicron sub-variants, present significant challenges in pandemic control due to their capacity to escape antibodies and breach vaccine protections. Discovering antibodies that can tolerate mutations in VOCs and understanding their underlying mechanisms is crucial for developing therapeutics for COVID-19 patients, particularly those for whom other therapies may be unsuitable. Here, we report the neutralization of the Omicron variant by FD20, a broadly active human monoclonal antibody. In contrast to a clinically approved control antibody, FD20 neutralizes Omicron with comparable IC values to those observed for previously circulating VOCs and the original strain reported in Wuhan. Leveraging structural information, we provide insights into its resilience against mutations in Omicron. The results encourage the prospective development of FD20 as a therapeutic option for COVID-19 caused by current and potentially future VOCs.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的关切变异株(VOCs),如奥密克戎亚变体,由于其能够逃避抗体并突破疫苗保护,给疫情防控带来了重大挑战。发现能够耐受VOCs突变的抗体并了解其潜在机制,对于开发针对新冠肺炎患者的治疗方法至关重要,尤其是对于那些可能不适合其他疗法的患者。在此,我们报告了一种广泛有效的人源单克隆抗体FD20对奥密克戎变异株的中和作用。与临床批准的对照抗体相比,FD20对奥密克戎的中和作用具有与先前流行的VOCs以及武汉报告的原始毒株相当的半数抑制浓度(IC)值。利用结构信息,我们深入了解了其对奥密克戎突变的耐受性。这些结果鼓励将FD20前瞻性地开发为针对当前及未来可能出现的VOCs引起的新冠肺炎的一种治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4ec/11740836/3d08d6a97175/44307_2024_11_Fig1_HTML.jpg

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